Preface
About the Authors
Almost 1,650 media are described in the second edition of the Handbook of Media for Clinical...
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Preface
About the Authors
Almost 1,650 media are described in the second edition of the Handbook of Media for Clinical Microbiology, including newly described media for the cultivation of emerging pathogens. Diseases caused by emerging pathogens that are responsible for increased rates of morbidity and mortality rates, such as Escherichia coli O157:H7, methicillin resistant Staphylococcus aureus, and vancomycin resistant enterococci, have raised special concerns and various media included in the Handbook have been designed for the specific cultivation and identification of these pathogens.
Ronald M. Atlas is Graduate Dean, Professor of Biology, and Professor of Public Health at the University of Louisville. He received his B.S. from the State University of New York at Stony Brook in 1968 and his M.S. and Ph.D. from Rutgers in 1970 and 1972, respectively. Dr. Atlas has received a number of honors including: The University of Louisville Excellence in Research Award, the Johnson and Johnson Fellowship for Biology, and the ASM Award in Applied and Environmental Microbiology. He has authored several microbiology textbooks and handbooks of microbiological media. His research has included development of diagnostic systems for pathogenic microorganisms. He has served on the editorial boards of Applied and Environmental Microbiology, BioScience, Biotechniques, Environmental Microbiology, Biosecurity, and Bioterrorism, and Journal of Industrial Microbiology. He is editor of Critical Reviews in Microbiology. He also has served as President of the American Society for Microbiology.
Many of the new media included in the second edition of the Handbook of Media for Clinical Microbiology permit the cultivation of bacteria, fungi, and viruses that are currently causing major medical problems around the world. These media are very important for the rapid detection of pathogenic microorganisms and the diagnosis of individuals with specific infectious diseases. Several of the new media described in the second edition of the Handbook of Media for Clinical Microbiology include chromogenic or fluorogenic substrates that permit the rapid detection of specific pathogens. An important function of the second edition of the Handbook of Media for Clinical Microbiology is to provide descriptions of the media that are used to cultivate and identify microorganisms from clinical specimens and to maintain reference cultures of human pathogens in various clinical settings. The Handbook provides a compilation of the formulations, methods of preparation, and applications for media used in the clinical microbiology laboratory. Each listing is alphabetical and includes medium composition, instruction for preparation, commercial sources, and intended uses. The format of the Handbook allows easy reference to information needed to prepare media for the cultivation of microorganisms relevant to clinical diagnostics. The second edition of the Handbook of Media for Clinical Microbiology includes descriptions of expected results as they apply to microorganisms of importance for the examination of clinical specimens. Importantly, the second edition of the Handbook of Media for Clinical Microbiology is user friendly and should save time and effort for anyone cultivating pathogenic microorganisms. It should be a valuable resource for anyone working in the area of clinical microbiology.
James W. Snyder is Professor of Pathology in the Department of Pathology and Laboratory Medicine at the University of Louisville School of Medicine and serves as the Director of Microbiology for the University of Louisville Hospital. He received his B.S. in 1969 and M.S. in 1970 from Eastern Kentucky University and Ph.D. in 1974 from the University of Dayton. Dr. Snyder is a diplomate of the American Board of Medical Microbiology (ABMM) and a Fellow in the American Academy of Microbiology. He has received a number of honors including: The South Central Association for Clinical Microbiology Outstanding Contribution to Microbiology Award, the Spirit of Louisville Foundation Award, Outstanding Service Award as Chairman of the Committee on Continuing Education of the American Society for Microbiology, and election to the Alpha Omega Alpha Honor Medical Society. He is the former Editor of The Yearbook of Clinical Microbiology and the Certified Clinical Microbiology Data Base. He is currently a member of the Critical Reviews in Microbiology editorial board and serves on the Professional Affairs Committee of the American Society for Microbiology. He maintains an active research program in both applied and basic clinical microbiology, including molecular techniques for the detection of pathogens and the assessment and comparison of automated and nonautomated diagnostic systems and tracking of microbial incidence and in vitro activity of antibiotics in support of local and national surveillance programs.
Table of Contents Diagnostic Microbiology: Isolation and Identification of Pathogens...........................1 Isolation and Culture Procedures.............................1 Media for the Isolation and Identification of Microorganisms from Clinical Specimens......2 References................................................................4 A 3 Agar...................................................................5 A 3B Agar................................................................5 A 7 Agar...................................................................6 A 7 Agar, Modified..................................................7 A 7B Agar................................................................7 A 8B Agar................................................................8 A 1 Broth .................................................................9 Abeyta-Hunt Bark Agar...........................................9 ABY Agar ..............................................................10 AC Agar.................................................................10 AC Broth................................................................10 Acanthamoeba Medium.........................................11 ACC Medium.........................................................11 Acetamide Agar .....................................................11 Acetamide Broth ....................................................11 Acetamide Cetrimide Glycerol Mannitol Selective Medium..............................................12 Acetamide Medium................................................12 Acetamide Medium................................................13 Acetate Differential Agar.......................................13 Acetobacteroides glycinophilus Medium...............13 Achromobacter Choline Medium ..........................14 Achromobacter Choline Medium, Modified.............................................14 Achromobacter Medium ........................................15 Acid Egg Medium..................................................15 Acid Tomato Broth ................................................15 Actidione® Agar....................................................15 Actinomyces Agar ..................................................16 Actinomyces Broth .................................................16 Actinomyces Isolation Agar ...................................16 Actinomycete Growth Medium .............................17 Activated Carbon Medium.....................................17 AE Sporulation Medium, Modified .......................17 Aeromonas Differential Agar.................................18 Aeromonas hydrophila Medium ............................18 Aeromonas Medium...............................................18 AFPA......................................................................19 AH5 Medium .........................................................19 AKI Medium..........................................................20 Alcaligenes Agar....................................................20 Alcaligenes Medium ..............................................20 Alcaligenes N5 Medium ........................................20 Alcaligenes NA YE Medium .................................21 Alcaligenes NB YE Agar .......................................21 Alcaligenes NB YE Broth......................................21 Alcaligenes NB YE Medium .................................21
Alginate Utilization Medium.................................21 Alkaline Peptone Agar...........................................22 Alkaline Peptone Salt Broth ..................................22 Alkaline Peptone Water .........................................22 Alkvisco Medium ..................................................22 Allantoin Agar .......................................................22 Allantoin Broth ......................................................23 ALOA Medium......................................................23 ALP Basal Medium ...............................................24 Amies Modified Transport Medium with Charcoal ....................................................24 Amies Modified Transport Medium with Charcoal ....................................................25 Amies Transport Medium without Charcoal .........25 AMO.1 Medium ....................................................25 Ampicillin Kanamycin Nutrient Agar ...................26 Ampicillin L Broth Medium..................................26 Ampicillin TY Salt Medium..................................27 Amygdalin Medium...............................................27 Anaerobe Agar.......................................................27 Anaerobe Agar.......................................................28 Anaerobe Medium .................................................28 Anaerobic Agar......................................................28 Anaerobic Agar......................................................29 Anaerobic Broth.....................................................29 Anaerobic CNA Agar ............................................29 Anaerobic Egg Yolk Agar......................................29 Anaerobic Egg Yolk Agar......................................30 Anaerobic LKV Blood Agar..................................30 Anaerobic Oxalate Medium...................................31 Anaerobic Trypticase™ Soy Agar with Calf Blood .................................................32 Anaerobic TVLS Medium .....................................32 Andersen’s Pork Pea Agar .....................................32 Andrade’s Carbohydrate Broth and Indicator........33 Andrade’s Broth.....................................................33 Anthracis Chromogenic Agar ................................34 Antibiotic Medium 1..............................................34 Antibiotic Medium 2..............................................34 Antibiotic Medium 3..............................................34 Antibiotic Medium 3 Plus......................................35 Antibiotic Medium 4..............................................35 Antibiotic Medium 5..............................................35 Antibiotic Medium 6..............................................35 Antibiotic Medium 7..............................................35 Antibiotic Medium 8..............................................36 Antibiotic Medium 9..............................................36 Antibiotic Medium 10............................................36 Antibiotic Medium 11............................................36 Antibiotic Medium 12............................................37 Antibiotic Medium 13............................................37 Antibiotic Medium 19............................................37 Antibiotic Medium 20............................................37
Antibiotic Medium 21............................................37 Antibiotic Sulfonamide Sensitivity Test Agar .......38 AOAC Letheen Broth ............................................38 Arenavirus Plaquing Medium................................38 Arginine Broth .......................................................39 Arginine Broth with NaCl......................................39 Arginine Glucose Slants ........................................39 Armstrong Fusarium Medium ...............................39 Arylsulfatase Agar .................................................39 Ascospore Agar......................................................40 ASM Medium ........................................................40 Asparaginate Glycerol Agar ..................................40 Asparagine Broth ...................................................40 Aspergillus Differential Medium ...........................40 Aspergillus Medium...............................................41 ATS Medium..........................................................41 AV Agar with Vitamins..........................................41 Avian Mycoplasma Agar........................................42 Avian Mycoplasma Broth ......................................42 Azide Blood Agar ..................................................43 Azide Blood Agar with Crystal Violet...................43 Azide Broth............................................................44 Azide Medium .......................................................44 B Broth...................................................................44 Bacillus cereus Medium ........................................44 Bacillus cereus Selective Agar Base......................45 Bacillus Medium....................................................45 Bacillus Medium....................................................46 Bacteroides Bile Esculin Agar...............................46 BAF Agar...............................................................47 BAGG Broth ..........................................................47 Baird-Parker Agar..................................................47 Baird-Parker Agar, Supplemented .........................48 Baird-Parker Medium ............................................48 Balamuth Medium .................................................48 Basal Synthetic Medium........................................49 Basic Cultivation Medium .....................................49 Basic Mineral Medium ..........................................49 BC Motility Medium .............................................49 BCM Bacillus cereus Group Plating Medium .......49 BCM O157:H7(+) Plating Medium.......................50 BCP D Agar ...........................................................50 BCP DCLS Agar....................................................50 BCYE Agar............................................................50 BCYE Differential Agar ........................................51 BCYE Medium, Diphasic Blood Culture ..............51 BCYE Selective Agar with CCVC ........................52 BCYE Selective Agar with GPVA.........................52 BCYE Selective Agar with GVPC ........................53 BCYE Selective Agar with PAC............................53 BCYE Selective Agar with PAV............................54 BCYEα with Alb ...................................................54 BCYEα without L-Cysteine...................................54 Beef Extract Agar ..................................................55 Beef Extract Broth .................................................55 Beef Extract Peptone Serum Medium ...................55
Beef Infusion Agar ................................................55 Beef Infusion Broth ...............................................56 Beef Liver Medium for Anaerobes........................56 Bennett’s Agar .......................................................56 Bennett’s Agar with Maltose .................................56 Bennett’s Modified Agar Medium.........................56 BG Sulfa Agar .......................................................56 BHI with Glucose ..................................................57 BHI Glucose Medium............................................57 BHI with Glycerol and Reducing Agents..............57 BHI Medium..........................................................58 BHI/1 Medium.......................................................58 BHI/2 Medium.......................................................58 BHI/3 Medium.......................................................58 Bifidobacterium Medium.......................................58 BiGGY Agar..........................................................59 Bile Esculin Agar...................................................59 Bile Esculin Agar with Kanamycin .......................60 Bile Esculin Azide Agar ........................................60 Bile Oxalate Sorbose Broth ...................................60 Bile Salts Brilliant Green Starch Agar...................61 Bile Salts Gelatin Agar ..........................................61 BIN Medium..........................................................62 Biosynth Chromogenic Medium for Listeria monocytogenes ...............................62 Biphasic Medium for Neisseria .............................62 Bird Seed Agar ......................................................63 Bismuth Sulfite Agar .............................................63 Bismuth Sulfite Agar Wilson and Blair .................63 Bismuth Sulfite Broth ............................................64 BL Agar .................................................................64 Blood Agar.............................................................64 Blood Agar Base....................................................65 Blood Agar Base No. 2..........................................65 Blood Agar Base with Peptone..............................66 Blood Agar Base, Sheep ........................................66 Blood Agar Base with Special Peptone .................66 Blood Agar, Diphasic ............................................66 Blood Agar, Diphasic Base Medium .....................67 Blood Agar with Low pH ......................................67 Blood Agar No. 2...................................................67 Blood Base Agar....................................................67 Blood Base Agar with Charcoal ............................67 Blood Base Agar with Horse Blood ......................68 Blood Base Agar with Horse Blood, Fumarate and Formate ................68 Blood Glucose Cystine Agar .................................68 BMPA-α Medium ..................................................68 BMPA-α Medium ..................................................69 Bonner-Addicott Medium......................................69 Bordetella pertussis Selective Medium with Bordet-Gengou Agar Base ........................69 Bordetella pertussis Selective Medium with Charcoal Agar Base...................................70 Bordet-Gengou Agar .............................................70 Bordet-Gengou Medium........................................71
Borrelia Medium ...................................................71 Bouillon Medium...................................................72 Bovine Albumin Tween 80 Medium, Ellinghausen and McCullough, Modified .........72 Bovine Albumin Tween 80 ....................................80 Semisolid Medium, Ellinghausen and McCullough, Modified ...............................72 Bovine Serum Albumin Tween 80 Agar................73 Bovine Serum Albumin Tween 80 Broth ..............73 Bovine Serum Albumin Tween 80 Soft Agar ........74 Brain Heart CC Agar .............................................74 Brain Heart Infusion ..............................................74 Brain Heart Infusion Agar .....................................75 Brain Heart Infusion Agar 0.7% ............................75 Brain Heart Infusion with 0.7% Agar....................76 Brain Heart Infusion Agar with Chloramphenicol ...............................................76 Brain Heart Infusion Agar with Kanamycin..........76 Brain Heart Infusion Agar with Penicillin and Streptomycin ......................76 Brain Heart Infusion Agar with 10% Sheep Blood, Gentamicin, and Chloramphenicol ........77 Brain Heart Infusion Agar with Tween 80.............77 Brain Heart Infusion with Agar, Yeast Extract, NaCl, Inactivated Horse Serum, and Penicillin..............................77 Brain Heart Infusion with Agar, Yeast Extract, Sucrose, Horse Serum, and Penicillin..............................78 Brain Heart Infusion with Agar, Yeast Extract, Sucrose, Inactivated Horse Serum, and Penicillin..............................78 Brain Heart Infusion Blood Agar...........................78 Brain Heart Infusion Broth ....................................79 Brain Heart Infusion with Casein ..........................79 Brain Heart Infusion Casein Starch .......................79 Brain Heart Infusion with Cystine .........................79 Brain Heart Infusion with Glucose and Horse Serum .........................80 Brain Heart Infusion with 5% NaCl ......................80 Brain Heart Infusion with PABA ...........................80 Brain Heart Infusion with PABA and Agar.........................................80 Brain Heart Infusion with Rabbit Serum ...............81 Brain Heart Infusion with 3% Sodium Chloride ...81 Brain Heart Infusion Soil Extract Medium............81 Brain Heart Infusion with Sucrose and Horse Serum ...............................................82 Brain Liver Heart Semisolid Medium ...................82 Brewer Anaerobic Agar .........................................82 Brewer Thioglycolate Medium..............................82 Brewer Thioglycolate Medium, Modified .............82 BRILA MUG Broth ...............................................83 Brilliant Green Agar ..............................................83 Brilliant Green Agar, Modified..............................83
Brilliant Green 2%-Bile Broth, Fluorocult® .......................................................84 Brilliant Green Lactose Bile Broth ........................84 Brilliant Green Phenol Red Agar...........................84 BROLACIN MUG Agar........................................84 Bromcresol Purple Broth .......................................85 Bromcresol Purple Dextrose Broth........................85 Bromthymol Blue Agar .........................................85 Bromthymol Blue Broth ........................................86 Brucella Agar.........................................................86 Brucella Agar Base Campylobacter Medium........87 Brucella Agar with Vitamin K1 .............................87 Brucella Albimi Broth with 0.16% Agar...............87 Brucella Albimi Broth with 0.16% Agar and 1% Glycine ........................................87 Brucella Albimi Broth with Formate and Fumarate...............................88 Brucella Albimi Broth with Sheep Blood .............88 Brucella Albimi Medium, Semisolid.....................88 Brucella Anaerobic Blood Agar ............................88 Brucella Blood Agar with Hemin and Vitamin K1 .........................................................89 Brucella Blood Culture Broth................................89 Brucella Broth .......................................................89 Brucella Broth with Additives...............................90 Brucella Broth with 0.16% Agar ...........................90 Brucella Broth Base Campylobacter Medium ......91 Brucella Broth, Modified.......................................91 Brucella FBP Agar ................................................91 Brucella FBP Broth ...............................................91 Brucella Medium Base ..........................................92 Brucella Medium, Selective ..................................92 Brucella Selective Medium ...................................92 Brucella Semisolid Medium with Cysteine.....................................................92 Brucella Semisolid Medium with Glycine ............93 Brucella Semisolid Medium with NaCl ................93 Brucella Semisolid Medium with Nitrate..............93 BSK Medium .........................................................94 BSK Medium, Modified ........................................94 BSK Medium, Revised ..........................................95 BTB Lactose Agar .................................................96 BTB Teepol® Agar................................................96 BTU Medium.........................................................97 Buffered Charcoal Yeast Extract Differential Agar ...............................................97 Buffered Enrichment Broth ...................................97 Buffered Peptone Water.........................................98 Burkholderia cepacia Agar....................................98 BYE Agar ..............................................................98 BYEB.....................................................................99 Caffeic Acid Ferric Citrate Test Medium ..............99 Caffeine Medium ...................................................99 CAL Agar ............................................................100 CAL Broth ...........................................................100
Calymmatobacterium granulomatis Semidefined Medium ......................................100 CAMG Broth .......................................................100 Campy THIO Medium.........................................100 Campylobacter Agar............................................101 Campylobacter Agar with 5 Antimicrobics and 10% Sheep Blood .............101 Campylobacter Agar, Blaser’s.............................101 Campylobacter Agar, Skirrow’s ..........................102 Campylobacter Blood-Free Agar Base Modified .................................................102 Campylobacter Blood-Free Selective Agar .................................................102 Campylobacter Charcoal Differential Agar .............................................103 Campylobacter Enrichment Broth .......................103 Campylobacter Enrichment Broth .......................104 Campylobacter fecalis Medium...........................105 Campylobacter fetus Medium..............................105 Campylobacter fetus Medium..............................106 Campylobacter fetus Selective Medium ..............106 Campylobacter Isolation Agar A.........................106 Campylobacter Isolation Agar B .........................107 Campylobacter Medium ......................................107 Campylobacter mucosalis Medium .....................107 Campylobacter rectus Medium............................108 Campylobacter Selective Medium, Blaser-Wang.....................................108 Campylobacter Selective Medium, Blaser-Wang.....................................109 Campylobacter Selective Medium, Butzler’s...........................................109 Campylobacter Selective Medium, Karmali’s..........................................110 Campylobacter Selective Medium, Preston’s ..........................................................110 Campylobacter sputorum Subspecies bubulus Medium ...........................110 Campylobacter sputorum Subspecies mucosalis Medium........................ 111 Campylobacter Thioglycolate Medium with 5 Antimicrobics ........................ 111 Candida BCG Agar Base..................................... 111 Candida Isolation Agar........................................112 Capnocytophaga Medium....................................112 Capnocytophaga II Medium................................112 Carbohydrate Fermentation Broth .......................112 Carbon Assimilation Medium..............................113 Carbon Assimilation Medium, Auxanographic Method for Yeast Identification ...................................................113 Carbon Utilization Test ........................................114 Cardiobacterium hominis Medium......................114 Carnitine Chloride Medium .................................114 Carrot Potato Dextrose Agar................................115
Cary and Blair Transport Medium....................... 115 Cary and Blair Transport Medium, Modified .......................... 115 Casamino Acids Yeast Extract Lincomycin Medium .......................... 116 Casamino Acids Yeast Extract Salts Broth, Gorbach........................... 116 Casein Agar ......................................................... 116 Casein Yeast Extract Glucose Agar ..................... 116 Casein Yeast Extract Glucose Broth .................... 117 Casman Agar Base............................................... 117 Casman Agar Base with Rabbit Blood ................ 117 CASO MUG Agar ............................................... 117 CCY Modified Medium....................................... 118 CDC Anaerobe Blood Agar................................. 118 CDC Anaerobe Blood Agar with Kanamycin and Vancomycin................... 118 CDC Anaerobe Blood Agar with Phenylethyl Alcohol................................ 119 CDC Anaerobe Laked Blood Agar with Kanamycin and Vancomycin................... 119 Cefiximine Rhamnose Sorbitol MacConkey Agar ............................................120 Cefsulodin Irgasan Novobiocin Agar ..................120 Cell Growth Medium...........................................121 Cellobiose Polymyxin B Colistin Agar, Modified...............................122 Cellobiose Polymyxin Colistin Agar ...................123 Cereal Agar..........................................................123 Cetrimide Agar, Non-USP ...................................123 Cetrimide Agar, USP ...........................................123 CF Assay Medium ...............................................123 CFAT Medium .....................................................124 CGY Agar............................................................124 CH 1 Medium ......................................................124 Chapman Stone Agar ...........................................125 Charcoal Agar......................................................125 Charcoal Agar with Horse Blood ........................125 Charcoal Agar with Horse Blood and Cepahalexin ..............................................125 Charcoal Blood Medium......................................126 Chlamydia Growth Medium ................................126 Chlamydia Isolation Medium ..............................127 Chlamydospore Agar ...........................................127 Chloramphenicol Ampicillin LB Medium...........127 Chloramphenicol Erythromycin LB Medium......128 Chloramphenicol L Broth Medium No. 1............128 Chloramphenicol L Broth Medium No. 2............128 Chloramphenicol L Broth Medium No. 3............129 Chloramphenicol LB Medium No. 1 ...................129 Chloramphenicol LB Medium No. 2 ...................129 CHO Medium Base..............................................129 Chocolate Agar ....................................................129 Chocolate Agar ....................................................130 Chocolate Agar, Enriched....................................130
Chocolate Agar, Enriched ....................................131 Chocolate Agar-Bartonella C-29.........................131 Chocolate II Agar.................................................132 Chocolate II Agar with Hemoglobin and IsoVitaleX............................132 Chocolate Tellurite Agar......................................132 Cholera Medium TCBS .......................................133 Cholic Acid Medium ...........................................133 Cholera Medium TCBS .......................................133 Chopped Meat Agar.............................................134 Chopped Meat Broth............................................134 Chopped Meat Broth with Carbohydrates ...........134 Chopped Meat Broth with Formate and Fumarate.............................134 Chopped Meat Broth with Vitamin K1 ........... 135 Chopped Meat Carbohydrate Medium ................135 Chopped Meat Glucose Agar...............................136 Chopped Meat Glucose Broth..............................136 Chopped Meat Glucose Medium .........................136 Chopped Meat Medium .......................................136 Chopped Meat Medium with Formate and Fumarate ...................................................137 Chopped Meat Medium, Modified ......................137 Chopped Meat Medium, Modified with Formate and Fumarate.............................138 Christensen Agar..................................................139 Christensen Citrate Agar......................................139 Christensen Citrate Agar, Modified .....................139 Christensen Citrate Sulfide Medium....................139 Christensen’s Urea Agar ......................................140 CHROMagar Candida .........................................140 CHROMagar E. coli ............................................140 CHROMagar ECC ...............................................140 CHROMagar Listeria ..........................................141 CHROMagar O157 ..............................................141 CHROMagar Orientation.....................................141 CHROMagar Salmonella.....................................141 CHROMagar Staph. aureus .................................141 CHROMagar Vibrio .............................................141 Chromogenic Candida Agar................................142 Chromogenic Listeria Agar .................................142 Chromogenic MRSA Agar ..................................142 Chromogenic Salmonella Esterase Agar .............143 Chromogenic Substrate Broth..............................143 Chromogenic Urinary Tract Infection (UTI) Medium..................................143 Chromogenic UTI Medium, Clear.......................144 CIN Agar..............................................................144 Citrate Medium, Koser’s Modified......................144 CLED Agar ..........................................................145 CLED Agar with Andrade Indicator....................145 Clostridia Medium ...............................................145 Clostridium botulinum Isolation Agar .................145 Clostridium difficile Agar ....................................146 Clostridium Medium............................................147
Clostridium Medium............................................148 Clostridium Medium............................................149 Clostridium novyi Blood Agar.............................149 Clostridium perfringens Agar, OPSP ..................150 Clostridium Selective Agar..................................150 CM3 Medium.......................................................150 CN Screen Medium .............................................151 Coagulase Agar Base...........................................151 Coagulase Mannitol Agar ....................................151 COBA ..................................................................151 Coletsos Medium .................................................152 Coletsos Selective Medium .................................152 Coliform Agar, Chromocult®..............................153 Coliform Agar ES, Chromocult...........................153 Columbia Agar.....................................................154 Columbia Blood Agar..........................................154 Columbia Blood Agar Base .................................154 Columbia Blood Agar Base with Horse Blood....................................155 Columbia Blood Agar Base with Horse Blood and Charcoal ......................155 Columbia Broth ...................................................155 Columbia Broth ...................................................156 Columbia CNA Agar ...........................................156 Columbia CNA Agar, Modified with Sheep Blood ....................................................157 Complex Medium ................................................157 Congo Red Acid Morpholinepropanesulfonic Acid Pigmentation Agar..................................157 Congo Red Agar ..................................................157 Congo Red Agar ..................................................158 Congo Red BHI Agarose Medium ......................158 Congo Red BHI Agarose Medium ......................159 Congo Red Magnesium Oxalate Agar.................159 Conradi Drigalski Agar........................................160 Converse Liquid Medium, Levine Modification .160 Cooke Rose Bengal Agar.....................................160 Cooked Meat Medium .........................................160 Cooked Meat Medium .........................................161 Cooked Meat Medium with Glucose, Hemin, and Vitamin K .....................161 Cooked Meat Medium, Modified ........................162 Cooked Meat Medium with Peptone and Yeast Extract.............................................162 Cornmeal Agar.....................................................162 Cornmeal Agar with Strep100 and Tet100 ..........162 Cornmeal Yeast Glucose Agar.............................163 CREA...................................................................163 Creatinine Agar....................................................163 Creatinine Medium ..............................................163 CreDm1 Medium .................................................164 Crystal Violet Agar ..............................................164 Crystal Violet Azide Esculin Agar ......................165 Crystal Violet Esculin Agar .................................165 CT Agar ...............................................................165
CTA Agar.............................................................166 CTA Medium .......................................................166 CTA Medium with Yeast Extract and Rabbit Serum .................................................166 CTLM Medium....................................................166 CVA Medium .......................................................167 Cycloserine Cefoxitin Egg Yolk Fructose Agar ..167 CYE Agar ............................................................167 CYE Agar, Buffered ............................................168 Cystine Heart Agar ..............................................168 Cystine Heart Agar with Rabbit Blood................169 Cystine Tellurite Blood Agar ...............................169 Czapek Dox Agar, Modified................................169 Czapek Dox Broth ...............................................170 Czapek Dox Liquid Medium, Modified ..............170 Czapek Solution Agar ..........................................170 Czapek Yeast Extract Agar ..................................170 DCLS Agar ..........................................................171 Decarboxylase Base, Møller ................................171 Decarboxylase Medium Base, Falkow ................171 Decarboxylase Medium, Ornithine Modified......171 Demi-Fraser Broth ...............................................172 Deoxycholate Agar ..............................................172 Deoxycholate Citrate Agar ..................................172 Deoxycholate Citrate Agar ..................................173 Deoxycholate Citrate Agar, Hynes ......................173 Deoxycholate Lactose Agar.................................173 Dermasel Agar Base ............................................174 Dermatophyte Test Medium Base........................174 DEV Lactose Peptone MUG Broth .....................174 Dextrose Agar ......................................................174 Dextrose Agar ......................................................175 Dextrose Ascitic Fluid Semisolid Agar ...............175 Dextrose Broth.....................................................175 Dextrose Proteose No. 3 Agar .............................175 Dextrose Starch Agar...........................................176 Diagnostic Sensitivity Test Agar .........................176 Diamonds Medium, Modified..............................177 Diethyl Phosphonate Agar ...................................177 Differential Agar Medium A8 for Ureaplasma urealyticum..........................177 Dilute Peptone Water ...........................................178 Dilute Potato Medium..........................................178 Diphasic Blood Agar Base Medium ....................178 Diphasic Blood Agar Medium with 10% Blood.............................................178 Diphasic Blood Agar Medium with 30% Blood.............................................179 Diphasic Medium for Amoeba.............................179 Dixon Agar ..........................................................180 DNase Agar..........................................................180 DNase Medium ....................................................180 DNase Test Agar ..................................................181 DNase Test Agar with Methyl Green...................181 DNase Test Agar with Toluidine Blue .................181
Dorset Egg Medium.............................................181 DTC Agar ............................................................181 DTM Agar ...........................................................182 Dulaney Slants .....................................................182 Duncan-Strong Sporulation Medium, Modified..182 Dunkelberg Carbohydrate Medium, Modified ....182 Dunkelberg Maintenance Medium ......................183 Dunkelberg Semisolid Carbohydrate Fermentation Medium ...................................183 E. coli O157:H7 MUG Agar................................183 Eagle Medium......................................................183 Eagle Medium......................................................184 Eagle Medium......................................................185 Eagle Medium, Modified.....................................185 Eagle’s Minimal Essential Medium with Earle’s Salts and Nonessential Amino Acids..186 Earle’s Balanced Salts, Phenol Red-Free.............187 EB Motility Medium............................................187 EC Broth ..............................................................187 EC Broth with MUG............................................187 EC Medium, Modified with Novobiocin.............187 ECD MUG Agar ..................................................188 Egg Yolk Agar .....................................................188 Egg Yolk Agar, Modified.....................................188 Egg Yolk Emulsion ..............................................189 Egg Yolk Emulsion, 50%.....................................189 Egg-yolk Tellurite Emulsion 20% .......................189 Eijkman Lactose Medium....................................189 EMB Agar............................................................190 EMB Agar Base...................................................190 EMB Agar, Modified ...........................................190 Endo Agar............................................................190 Endo Agar............................................................191 Endo Agar, LES ...................................................191 Endo Broth...........................................................192 Enriched Nutrient Broth ......................................192 Enrichment Broth for Aeromonas hydrophila .....192 Entamoeba Medium.............................................192 Enteric Fermentation Base...................................193 Enterobacter Medium..........................................193 Enterococci Broth, Chromocult ...........................193 Enterococcosel™ Agar ........................................194 Enterococcosel Broth...........................................194 Enterococcus Agar...............................................194 Enterococcus faecium Medium ...........................195 Erythritol Agar.....................................................195 Erythritol Broth....................................................195 Esculin Agar ........................................................195 Esculin Agar, Modified CDC ..............................195 Esculin Broth .......................................................195 Esculin Iron Agar.................................................196 Esculin Mannitol Agar.........................................196 ETGPA.................................................................196 Ethyl Violet Azide Broth .....................................197 Eubacterium Medium ..........................................198
Fastidious Anaerobe Agar ...................................198 Fastidious Anaerobe Agar, Alternative Selective..198 Fastidious Anaerobe Agar, Alternative Selective with Neomycin, Vancomycin, and Josamycin ...............................................199 Fastidious Anaerobe Agar, Selective ...................199 Fastidious Anaerobe Agar, Selective with Neomycin and Vancomycin...........................200 Fay and Barry Medium ........................................200 FDA Agar ............................................................201 FDA Broth ...........................................................201 Fecal Coliform Agar, Modified ...........................201 Fermentation Broth ..............................................201 Fermentation Medium..........................................202 F-G Agar ..............................................................202 F-G Agar with Selenium......................................202 F-G Broth.............................................................203 FGTC Agar...........................................................203 Fildes Enrichment Agar .......................................204 Fish Peptone Agar................................................204 Fish Peptone Broth...............................................204 Five g Agar ..........................................................205 Fletcher Medium..................................................205 Fletcher Medium with Fluorouracil.....................205 Fletcher’s Semisolid Medium ..............................205 FLN Medium .......................................................205 Fluid Sabouraud Medium ....................................206 Fluid Thioglycolate Agar.....................................206 Fluid Thioglycolate Agar with Calcium Carbonate ........................................206 Fluid Thioglycolate Medium ...............................206 Fluid Thioglycolate Medium with Beef Extract...........................................207 Fluid Thioglycolate Medium without Glucose or Eh Indicator ....................207 Fluid Thioglycolate Medium with K Agar ...................................................207 Fluid Thioglycolate Medium with Rabbit Serum.........................................207 Fluorocult E. coli 0157:H7 Agar .........................208 FN Medium..........................................................208 Folic Acid Agar ...................................................208 Formate Fumarate Medium .................................209 FRAG Agar..........................................................209 Francisella tularensis Isolation Medium.............210 Freezing Medium.................................................210 G Medium ............................................................210 GAM Agar ...........................................................211 GAM Semisolid ...................................................211 Gardnerella vaginalis Selective Medium ............211 GBNA Medium....................................................211 GBS Agar Base, Islam .........................................212 GBS Medium, Rapid............................................212 GC Agar...............................................................212 GC Agar...............................................................213
GC Agar with Ampicillin ....................................214 GC Agar with Ampicillin and Gentamicin..........215 GC Agar with Ampicillin and Tetracycline.........215 GC Agar with Chloramphenicol, Tetracycline, and Ampicillin .........................216 GC Agar with Defined Supplements ...................217 GC Agar with Penicillin G ..................................217 GC Agar with Supplement A...............................218 GC Agar with Supplement A and with VCN Inhibitor.................................219 GC Agar with Supplement A and with VCTN Inhibitor .....................................219 GC Agar with Supplement B...............................220 GC Medium, New York City Formulation ..........221 GCII Agar ............................................................221 GCII Agar ............................................................222 GC-Lect™ Agar ..................................................222 GC Medium with Chloramphenicol ....................223 GCA Agar with Thiamine ...................................223 Gelatin Agar.........................................................224 Gelatin Infusion Broth .........................................224 Gelatin Medium ...................................................225 Gelatin Metronidazole Cadmium Medium..........225 Gelatin Phosphate Salt Agar................................225 Gelatin Phosphate Salt Broth...............................226 Gelatin Salt Agar .................................................226 Gelatinase Test Medium ......................................226 Gluconate Peptone Broth.....................................226 Glucose Nutrient Agar.........................................226 Glucose Phosphate Broth.....................................227 Glucose Salt Teepol Broth ...................................227 Glucose Salts Medium.........................................227 Glutarate Medium................................................227 Glycerol Agar ......................................................228 Glycerol Asparagine Meat Agar..........................228 GN Broth, Hajna..................................................228 Gonococcus Medium ...........................................229 GP Agar ...............................................................229 GPHF Agar ..........................................................229 Granada Medium .................................................229 Group A Selective Strep Agar with Sheep Blood ..........................................230 H Agar .................................................................230 H Broth ................................................................231 H Diphasic Medium.............................................232 Haemophilus ducreyi Medium.............................233 Haemophilus ducreyi Medium, Revised..............233 Haemophilus influenzae Defined Medium MI ....234 Haemophilus influenzae Defined Medium MI-Cit............................................................234 Haemophilus Medium .........................................235 Haemophilus Test Medium..................................235 Ham’s F-10 Medium............................................236 HBT Bilayer Medium ..........................................236 Heart Infusion Agar .............................................237
Heart Infusion Agar with Glucose .......................238 Heart Infusion Agar with 0.1% Glucose..............238 Heart Infusion Agar (pH 7.6) with Inactivated Horse Serum .......................238 Heart Infusion Agar with Inactivated Horse Serum ..................................................238 Heart Infusion Agar with Inactivated Horse Serum, NaCl, and Penicillin ...............238 Heart Infusion Agar with Rabbit Blood...............239 Heart Infusion Broth ............................................239 Heart Infusion Broth (pH 7.5) with Inactivated Human Serum and Yeast Extract..................................................239 Heart Infusion Broth with Additives for Staphylococcus ................239 Heart Infusion Broth with Additives for Streptobacillus.................239 Heart Infusion Broth with Inactivated Horse Serum and Fresh Yeast Extract ...........240 Heart Infusion Broth with Inactivated Horse Serum, Fresh Yeast Extract, and Sucrose....................................................240 Heart Infusion Medium with Fetal Bovine Serum ...............................240 Heart Infusion Tyrosine Agar ..............................240 Hektoen Enteric Agar ..........................................241 Helicobacter pylori Isolation Agar ......................241 Helicobacter pylori Selective Medium................241 Hemo ID Quad Plate with Growth Factors..........242 Hemorrhagic Coli Agar .......................................242 Herellea Agar.......................................................242 Hershey’s Tris-Buffered Salts Medium ...............243 Hexamita Medium ...............................................243 HiCrome™ Aureus Agar Base ............................244 HiCrome Coliform Agar......................................244 HiCrome Coliform Agar with Novobiocin..........245 HiCrome E. coli Agar A ......................................245 HiCrome E. coli Agar B ......................................245 HiCrome ECC Agar.............................................245 HiCrome ECC Selective Agar .............................246 HiCrome Enterococci Broth ................................247 HiCrome Listeria Agar Base, Modified ..............247 HiCrome MacConkey-Sorbitol Agar...................247 HiCrome MacConkey-Sorbitol Agar with Tellurite-Cefixime Supplement .............248 HiCrome M-CP Agar Base ..................................248 HiCrome MS.O157 Agar.....................................249 HiCrome MS.O157 Agar with Tellurite ..............249 HiCrome Rapid Coliform Broth ..........................249 HiCrome Rapid Enterococci Agar.......................250 HiCrome Salmonella Agar...................................250 HiCrome Salmonella Chromogen Agar...............250 HiCrome UTI Agar, Modified .............................250 Histoplasma capsulatum Agar.............................251 Histoplasma capsulatum Agar.............................252
Histoplasma capsulatum Broth............................253 HL Agar ...............................................................254 HO-LE Trace Elements Solution.........................254 Horse Blood Agar ................................................254 Horse Serum Agar ...............................................255 Horse Serum Broth ..............................................255 Hoyle Medium .....................................................255 Hoyle Medium Base ............................................255 HR Antifungal Assay Medium Buffered with MOPS.....................................256 Hugh-Leifson’s Glucose Broth ............................256 Hydroxybenzoate Agar........................................256 Hydroxybenzoate Broth.......................................257 Imidazole Utilization Medium.............................257 Indole Medium.....................................................258 Indole Nitrite Medium .........................................258 Infection Medium ................................................258 Infusion Broth......................................................258 Inhibitory Mold Agar...........................................259 Inositol Brilliant Green Bile Salts Agar...............259 Inositol Urea Caffeic Acid Medium ....................259 Intracellular Growth Phase Medium....................260 Ion Agar for Ureaplasma.....................................260 Irgasan Ticarcillin Chlorate Broth .......................261 Iron Agar, Lyngby................................................261 Iron Milk Medium ...............................................261 Iso-Sensitest Agar................................................261 Iso-Sensitest Broth...............................................262 Isoleucine Hydroxamate Medium........................262 Jones-Kendrick Pertussis Transport Medium ......262 Jordan’s Tartrate Agar..........................................263 Kanamycin Vancomycin Blood Agar ..................263 Kanamycin Vancomycin Laked Blood Agar .......263 Kasai Medium......................................................264 KCN Broth...........................................................264 Keister's Modified TYI-S-33 Medium ................264 Kelly Medium, Nonselective Modified ...............264 Kelly Medium, Selective Modified .....................265 KF Streptococcus Agar ........................................266 KF Streptococcus Agar ........................................267 KF Streptococcus Broth .......................................267 Kirchner’s Enrichment Medium ..........................267 K-L Virulence Agar .............................................268 Klebsiella Medium...............................................269 Klebsiella Selective Agar ....................................269 Kligler Iron Agar .................................................270 Knisely Medium for Bacillus anthracis ..............270 Koch’s K1 Medium..............................................270 Korthof Medium ..................................................271 Korthof Medium, Modified .................................271 Koser Citrate Medium .........................................271 Kosmachev’s Medium .........................................271 Kupferberg Trichomonas Base ............................271 Kupferberg Trichomonas Broth ...........................272 L Agar..................................................................272
L Broth.................................................................272 L Diphasic Blood Agar Medium .........................272 L Diphasic Blood Agar Medium .........................273 Lab-Lemco Agar..................................................273 Lactose Broth .......................................................273 Lactose Egg Yolk Milk Agar ...............................274 Lactose Gelatin Medium......................................274 Lash Serum Medium............................................274 Lauryl Sulfate Broth ............................................275 Lauryl Sulfate Broth with MUG..........................275 LB Agar ...............................................................275 Lead Acetate Agar ...............................................275 Lecithin Lactose Agar..........................................276 Lecithin Lipase Anaerobic Agar..........................276 Lecithin Tween Medium ......................................276 Legionella Agar Base...........................................277 Legionella pneumophila Medium........................277 Legionella Selective Agar....................................277 Leishmania Medium ............................................278 Leptospira Medium..............................................278 Leptospira Medium, EMJH .................................278 Leptospira Medium, Modified.............................279 Leptospira Protein-Free Medium.........................279 Leptotrichia buccalis Medium.............................279 Leptotrichia Medium ...........................................280 Letheen Agar........................................................280 Letheen Agar, Modified.......................................280 Letheen Broth ......................................................281 Letheen Broth, Modified......................................281 Levine EMB Agar................................................281 Levinthal’s Agar ..................................................281 Listeria Enrichment Broth ...................................281 Listeria Fermentation Broth.................................282 Listeria Transport Enrichment Medium ..............282 LIT Medium.........................................................282 Litmus Milk .........................................................282 Littman Oxgall Agar ............................................283 Liver Broth...........................................................283 Liver Infusion Agar .............................................283 Liver Infusion Broth ............................................283 Liver Veal Agar....................................................283 Liver Veal Egg Yolk Agar....................................284 LMX Broth Modified, Fluorocult........................284 Loeffler Blood Serum Medium............................284 Loeffler Blood Serum Medium............................285 Loeffler Medium..................................................285 Loeffler Slant .......................................................285 Loeffler Slant, Modified ......................................285 Lombard–Dowell Agar ........................................286 Lombard-Dowell Bile Agar .................................286 Lombard-Dowell Broth........................................286 Lombard-Dowell Egg Yolk Agar.........................287 Lombard-Dowell Esculin Agar............................287 Lombard-Dowell Gelatin Agar ............................287 Lombard-Dowell Neomycin Agar .......................288
Long-Term Preservation Medium........................288 Low Iron YC Agar...............................................289 Low Iron YC Broth..............................................289 Lowenstein-Gruft Medium ..................................290 Lowenstein-Jensen Medium ................................290 Lowenstein-Jensen Medium without Glycerol....291 Lowenstein-Jensen Medium with Streptomycin .291 LPM Agar ............................................................291 LPM Agar with Esculin and Ferric Iron ..............292 LST-MUG Broth..................................................292 Lysine Arginine Iron Agar...................................292 Lysine Broth Falkow with NaCl ..........................293 Lysine Decarboxylase Broth, Falkow..................293 Lysine Decarboxylase Broth, Taylor Modification.......................................293 Lysine Decarboxylase Broth, Taylor Modification.......................................293 Lysine Decarboxylase Medium ...........................293 Lysine Iron Agar ..................................................293 Lysine Ornithine Mannitol Agar..........................294 M7 Medium .........................................................294 M9 Medium with Casamino Acids......................295 MacConkey Agar.................................................295 MacConkey Agar, CS ..........................................296 MacConkey Agar No. 2.......................................296 MacConkey Agar No. 3.......................................296 MacConkey Agar without Crystal Violet ............296 MacConkey Agar, Fluorocult ..............................297 MacConkey Agar without Salt ............................297 MacConkey MUG Agar ......................................297 Magnesium Oxalate Agar ....................................297 Maintenance of L Antigen in Neisseria...............297 Malachite Green Broth ........................................298 Malonate Broth ....................................................298 Malonate Broth, Ewing Modified........................298 Malt Agar.............................................................298 Mannitol Salt Agar ..............................................298 Martin-Lewis Agar ..............................................299 Martin-Lewis Agar, Enriched ..............................299 Maximum Recovery Diluent ...............................300 McBride Listeria Agar.........................................300 McCarthy Agar ....................................................300 McClung Carbon-Free Broth...............................301 McClung-Toabe Agar ..........................................301 McClung-Toabe Agar, Modified .........................301 McClung-Toabe Agar, Modified .........................302 McClung-Toabe Egg Yolk Agar, CDC Modified..302 m-CP Medium .....................................................303 Membrane Lactose Glucuronide Agar.................303 Methylene Blue Milk Medium ............................304 MH IH Agar.........................................................304 Middlebrook 13A Medium ..................................304 Middlebrook ADC Enrichment ...........................305 Middlebrook 7H9 Broth with Middlebrook ADC Enrichment.....................305
Middlebrook 7H9 Broth with Middlebrook OADC Enrichment ..................305 Middlebrook 7H9 Broth with Middlebrook OADC Enrichment and Triton WR 1339 ......................................306 Middlebrook 7H9 Broth, Supplemented..............306 Middlebrook 7H10 Agar with Middlebrook ADC Enrichment .....................307 Middlebrook 7H10 Agar with Middlebrook OADC Enrichment ..................307 Middlebrook 7H10 Agar with Middlebrook OADC Enrichment and Hemin .....................308 Middlebrook 7H10 Agar with Middlebrook OADC Enrichment and Triton WR 1339 ......................................308 Middlebrook 7H10 Agar with Streptomycin .......309 Middlebrook 7H11 Agar, Selective .....................309 Middlebrook 7H11 Agar with Middlebrook ADC Enrichment .....................310 Middlebrook 7H11 Agar with Middlebrook OADC Enrichment ..................310 Middlebrook 7H11 Agar with Middlebrook OADC Enrichment and Triton WR 1339 ......................................311 Middlebrook 7H12 Medium ................................311 Middlebrook Medium ..........................................312 Middlebrook Medium with Mycobactin..............312 Middlebrook OADC Enrichment.........................313 Middlebrook OADC Enrichment with Triton WR 1339.....................................313 MIL Medium........................................................313 Minimum Essential Medium with Bicarbonate, Serum, and Antibiotics.............313 Mitis-Salivarius Agar...........................................314 Møller Decarboxylase Broth................................315 Molybdate Agar ...................................................315 Monsur Agar ........................................................315 Motility GI Medium.............................................315 Motility Indole Ornithine Medium ......................316 Motility Medium S...............................................316 Motility Nitrate Agar ...........................................316 Motility Nitrate Medium......................................316 Motility Nitrate Medium......................................317 Motility Nitrate Medium, Buffered......................317 Motility Sulfide Medium .....................................317 Motility Test and Maintenance Medium..............317 Motility Test and Maintenance Medium, Gilardi ..318 Motility Test and Maintenance Medium, Tatum ...318 Motility Test Medium ..........................................318 Motility Test Medium, Semisolid ........................318 MRS Agar ............................................................319 MRS Broth...........................................................319 MRVP Broth ........................................................319 MRVP Medium....................................................319 Mucate Broth .......................................................319
Mucate Control Broth ..........................................320 Mueller-Hinton Agar ...........................................320 Mueller-Hinton Agar with IsoVitaleX and Hemoglobin..........................320 Mueller-Hinton Broth ..........................................320 Mueller-Hinton Chocolate Agar ..........................321 Mueller-Hinton II Agar........................................321 MUG Tryptone Soya Agar ..................................321 Muller-Kauffmann Tetrathionate Broth...............321 MWY Medium.....................................................322 Mycin Assay Agar ...............................................322 Mycobacterium Agar ...........................................322 Mycobactin Medium............................................322 Mycobactosel™ Agar ..........................................323 Mycobactosel L-J Medium ..................................324 Mycobiotic Agar..................................................324 Mycological Agar ................................................324 Mycological Agar with Low pH..........................324 Mycological Broth ...............................................325 Mycophil™ Broth................................................325 Mycoplasma Agar................................................325 Mycoplasma Agar Base .......................................326 Mycoplasma Agar with Increased Selectivity .....326 Mycoplasma Agar with Supplement G................326 Mycoplasma Agar with Supplement P ................327 Mycoplasma Broth...............................................327 Mycoplasma Broth Base......................................328 Mycoplasma Broth, Supplemented......................328 Mycoplasma Broth with Supplement G ..............328 Mycoplasma Broth with Supplement P ...............329 Mycoplasma Horse Serum Broth.........................329 Mycoplasma pneumoniae Isolation Medium.......329 Mycoplasmal Agar...............................................330 Neisseria Medium................................................330 Neisseria meningitidis Medium...........................330 Nelson Culture Medium for Naegleria................330 Nelson Culture Medium for Naegleria................331 Nelson Medium for Naegleria fowleri ................331 Neomycin Agar, Modified ...................................331 Neomycin Blood Agar.........................................331 Neomycin Luria Agar ..........................................332 Neomycin Medium No. 1 ....................................332 Neopeptone Glucose Agar...................................332 Neopeptone Glucose Rose Bengal Aureomycin® Agar.......................................332 Neopeptone Infusion Agar...................................333 New York City Medium ......................................333 New York City Medium, Modified......................334 NIH Agar .............................................................335 NIH Thioglycolate Broth.....................................335 Nitrate Agar .........................................................335 Nitrate Broth ........................................................335 Nitrate Broth ........................................................336 Nitrate Broth, Campylobacter .............................336 Nitrate Reduction Broth.......................................336
Nitrate Reduction Broth, Clark............................336 Nitrate Reduction Broth for Pseudomonas and Related Genera ................337 NNN Medium ......................................................337 Nonfat Dry Milk, Reconstituted ..........................337 Nonnutrient Agar Plates.......................................337 NOS Medium, Modified ......................................337 NOS Spirochete Medium.....................................338 Novobiocin Agar..................................................338 Nutrient Agar .......................................................339 Nutrient Agar with Formate, Fumarate, and Horse Blood ............................................339 Nutrient Agar No. 2 .............................................339 Nutrient Agar with Dihydrostreptomycin............339 Nutrient Agar with Horse Serum .........................340 Nutrient Agar with 0.5% NaCl ............................340 Nutrient Agar with 2% NaCl ...............................340 Nutrient Agar with Yeast Extract.........................340 Nutrient Broth ......................................................340 Nutrient Broth ......................................................341 Nutrient Broth No. 2 ............................................341 Nutrient Broth, Standard II ..................................341 Nutrient Gelatin ...................................................341 N-Z Amine A™ Glycerol Agar ...........................341 N-Z Amine A Medium with Soluble Starch and Glucose...................341 NZY Agar ............................................................342 NZY Agar ............................................................342 NZY Broth ...........................................................342 O157:H7(+) Plating Medium...............................342 O157:H7 ID Agar ................................................342 Oatmeal Agar .......................................................343 Ogawa TB Medium .............................................343 Oleic Albumin Complex......................................343 Önöz Salmonella Agar.........................................343 ONPG Broth ........................................................344 OR Indicator Agar ...............................................344 Oral Fusobacterium Medium...............................344 Oral Treponema Medium .....................................345 Organic Acid Medium KP ...................................345 Ornithine Broth ....................................................345 Ornithine Broth with NaCl ..................................345 Oxford Agar .........................................................346 Oxford Agar, Modified ........................................346 Oxidation-Fermentation Medium ........................346 Oxidation-Fermentation Medium, Hugh-Leifson’s ..............................................347 Oxidation-Fermentation Medium, King’s............347 Oxidative-Fermentative Medium.........................347 Oxidative-Fermentative Glucose Medium, Semisolid .........................348 Oxidative-Fermentative Glucose Medium, Semisolid, with NaCl.......348 Oxidative-Fermentative Test Medium .................348 P Agar ..................................................................348
Pagano Levin Agar ..............................................348 Pai Medium..........................................................349 PALCAM Agar ....................................................349 Pasteurella haemolytica Selective Medium ........350 Pasteurella multocida Selective Medium............350 PDM-114 Medium ...............................................350 Peptone Iron Agar................................................351 Peptone Meat Extract Soil Extract Agar..............352 Peptone Starch Dextrose Agar.............................352 Peptone Water ......................................................352 Peptone Water with Andrade’s Indicator .............352 Peptone Yeast Trypticase Agar ............................353 Petragnani Medium..............................................353 Pfizer Selective Enterococcus Agar ....................353 PGA .....................................................................354 PGP Broth............................................................354 PGT Medium........................................................354 Phenol Red Agar..................................................354 Phenol Red Agar..................................................355 Phenol Red Broth.................................................355 Phenol Red Glucose Broth...................................355 Phenol Red Lactose Agar ....................................355 Phenol Red Lactose Broth ...................................356 Phenol Red Mannitol Agar ..................................356 Phenol Red Mannitol Broth .................................356 Phenol Red Sucrose Broth ...................................356 Phenol Red Tartrate Agar ....................................357 Phenol Red Tartrate Broth ...................................357 Phenylalanine Agar..............................................357 Phenylalanine Malonate Broth ............................357 Phenylethanol Agar .............................................357 Phenylethanol Blood Agar...................................358 PHYG Medium....................................................358 Pike Streptococcal Broth .....................................358 Pine and Drouhet’s Histoplasma Yeast Phase Medium .....................................358 Pisu Medium........................................................360 PKU Test Agar.....................................................360 Plate Count MUG Agar .......................................361 PLET Agar...........................................................361 Poly-β-Hydroxybutyrate Medium .......................362 Polymyxin Staphylococcus Medium ...................362 Porcine Heart Agar ..............................................362 Potassium Cyanide Broth ....................................362 Potassium Tellurite Agar .....................................363 Potato Dextrose Yeast Agar .................................363 Potato Extract Agar..............................................363 PPLO Agar...........................................................363 PPLO Broth with Crystal Violet ..........................364 PPLO Broth without Crystal Violet.....................364 PPLO Broth without Crystal Violet with Calf Serum, Fresh Yeast Extract, and Sodium Acetate.........................364 Presumpto Media .................................................364 Proteose No. 3 Agar.............................................365
Proteose No. 3 Agar.............................................366 Proteose Yeast Extract Medium...........................366 Pseudomonas Agar F ...........................................366 Pseudomonas Agar P ...........................................366 Pseudomonas Basal Mineral Medium .................367 Pseudomonas CFC Agar......................................367 Pseudomonas CN Agar........................................367 Purple Agar ..........................................................368 Purple Broth.........................................................368 Purple Lactose Agar.............................................369 Purple Serum Agar Base......................................369 PV Blood Agar.....................................................369 PY Basal Medium................................................369 Pyrazinamidase Agar ...........................................370 Pyrazinamide Medium.........................................370 Pyruvate Utilization Medium...............................370 Pyruvic Acid Egg Medium ..................................370 R Medium ............................................................371 Rabbit Blood Agar ...............................................371 Rabbit Heart Infusion Agar..................................371 Rabbit Serum Medium.........................................371 Rainbow Agar O157 ............................................372 RAMBACH® Agar .............................................372 Rapid Fermentation Medium ...............................373 RAPID´E. coli 2 Agar..........................................373 RAPID´Enterococcus Agar .................................373 RAPID´L. mono Medium ....................................373 Rappaport Broth, Modified..................................373 Rappaport-Vassiliadis Enrichment Broth.............374 Rappaport-Vassiliadis R10 Broth.........................374 Rappaport-Vassiliadis Soya Peptone Broth .........374 Reactivation with Tryptone Soya Broth ..............374 Reduced Transport Fluid......................................375 Regan-Lowe Charcoal Agar ................................375 Regan-Lowe Semisolid Transport Medium.........375 Reinforced Clostridial Agar.................................376 Reinforced Clostridial Medium ...........................376 Reinforced Clostridial Medium with Sodium Lactate......................................376 Rice Extract Agar.................................................376 Rice Extract Agar.................................................377 Rimler-Shotts Medium.........................................377 RIOT Agar ...........................................................377 Rogosa Agar ........................................................377 Rogosa SL Agar...................................................378 Rogosa SL Broth..................................................378 RPMI 1640 Medium with L-Glutamine...............378 Russell Double-Sugar Agar .................................379 SABHI Agar ........................................................379 SABHI Agar, Modified........................................380 SABHI Blood Agar..............................................380 Sabouraud Agar ...................................................380 Sabouraud Agar with CCG and 3% NaCl ...........380 Sabouraud Agar with CCG and 5% NaCl ...........381 Sabouraud Glucose Agar, Emmons .....................381
Sabouraud Glucose Broth ....................................381 Sabouraud Maltose Agar .....................................381 Sabouraud Maltose Broth ....................................382 Sabouraud Medium, Fluid ...................................382 Salmonella Chromogen Agar ..............................382 Salmonella Chromogenic Agar............................382 Salmonella Rapid Test Elective Medium ............383 Salmonella Rapid Test Elective Medium, 2X......383 Salmonella Shigella Agar ....................................383 Salmonella Shigella Agar, Modified ...................383 Salt Meat Broth....................................................383 Salt Tolerance Medium........................................384 Salt Tolerance Medium, Gilardi ..........................384 Salt Tolerance Medium, Tatum............................384 Sauton’s Medium .................................................385 SBG Enrichment Broth........................................385 SBG Sulfa Enrichment ........................................385 SCGYEM Medium ..............................................385 Schaedler Agar.....................................................385 Schaedler Agar.....................................................386 Schaedler Agar with Vitamin K1 and Sheep Blood ..................................................386 Schaedler Broth ...................................................386 Schaedler CNA Agar with Vitamin K1 and Sheep Blood............................................386 Schaedler KV Agar with Vitamin K1 and Sheep Blood ................387 Schleifer-Krämer Agar ........................................387 Selenite Broth ......................................................387 Selenite Broth Base, Mannitol.............................388 Selenite Cystine Broth .........................................388 Selenite F Broth ...................................................388 Semisolid Brucella Broth ....................................388 Semisolid Medium for Motility ...........................388 Sensitest Agar ......................................................389 Serratia Differential Medium ..............................389 Serratia Hd-MHr .................................................389 Serratia Medium..................................................390 Serum Glucose Agar............................................390 Serum Glucose Agar, Farrell Modified ...............390 Serum Potato Infusion Agar ................................391 Serum Tellurite Agar ...........................................391 Seven H11 Agar...................................................392 SF Broth...............................................................392 Shigella Broth ......................................................392 Sierra Medium .....................................................393 SIM Medium........................................................393 Simmons’ Citrate Agar ........................................393 Skim Milk Agar ...................................................394 Skirrow Brucella Medium ...................................394 SM ID2 Agar .......................................................394 Snyder Agar .........................................................394 Snyder Test Agar .................................................394 Sodium Chloride Broth, 6.5.................................395 Sodium Chloride Sucrose Medium 900...............395
Sodium Chloride Sucrose Medium 900 with Penicillin G ......................395 Sodium Hippurate Broth......................................395 Soft Agar Gelatin Overlay ...................................396 Sorbitol MacConkey Agar ...................................396 Sorbitol MacConkey Agar with BCIG ................396 Soy Peptone Broth ...............................................397 Specimen Preservative Medium ..........................397 Spray’s Fermentation Medium.............................397 SPS Agar..............................................................397 SS Deoxycholate Agar.........................................397 ST Holding Medium ............................................398 Standard Fluid Medium 10B................................398 Standard II Nutrient Agar ....................................399 Staphylococcus Agar No. 110 ..............................399 Staphylococcus Broth...........................................399 Staphylococcus Medium ......................................399 Staphylococcus Medium No. 110 ........................399 Staphylococcus/Streptococcus Selective Medium...400 Starch Agar ..........................................................400 Starch Agar with Bromcresol Purple ...................400 Starch Agar with Bromcresol Purple ...................401 Starch Hydrolysis Agar........................................401 Sterility Test Broth...............................................401 Stock Culture Agar ..............................................401 Stock Culture Agar with L-Asparagine................402 Stonebrink’s Medium...........................................402 Strep ID Quad Plate .............................................402 StrepB Carrot Broth™ .........................................403 Streptococcal Growth Medium ............................403 Streptococcus Agar ..............................................403 Streptococcus Blood Agar, Selective ...................403 Streptococcus Medium.........................................404 Streptococcus pneumoniae Medium ....................404 Streptococcus Selective Medium .........................404 Streptosel™ Agar.................................................404 Streptosel Broth ...................................................405 Stuart Leptospira Broth, Modified.......................405 Stuart Medium Base.............................................405 Stuart Transport Medium .....................................405 Stuart Transport Medium, Modified ....................405 Sucrose Phosphate Glutamate Transport Medium .........................................406 Sucrose Phosphate Transport Medium ................406 Sucrose Teepol Tellurite Agar .............................406 Sucrose Yeast Extract Medium ............................406 Tap Water Agar ....................................................407 Tarshis Blood Agar ..............................................407 TB Nitrate Reduction Broth.................................407 TBX Agar ............................................................407 TCBS Agar ..........................................................407 TCH Medium.......................................................408 Tellurite Glycine Agar .........................................408 Tellurite Glycine Agar .........................................409 Tergitol 7 Agar .....................................................409
Tergitol 7 Agar H.................................................410 Tergitol 7 Broth....................................................410 Tetrathionate Broth ..............................................410 Tetrathionate Broth .............................................. 411 Tetrathionate Broth, Hajna...................................412 Tetrathionate Broth with Novobiocin ..................412 Tetrathionate Broth, USA ....................................412 Tetrathionate Crystal Violet Enhancement Broth...412 Tetrathionate Reductase Test Medium.................413 Tetrazolium Thallium Glucose Agar ...................413 Tetrazolium Tolerance Agar ................................413 Thayer-Martin Agar, Modified ............................413 Thayer-Martin Medium .......................................414 Thayer-Martin Medium, Modified ......................415 Thayer-Martin Medium, Selective.......................416 Thayer-Martin Selective Agar .............................417 Thiogel® Medium ...............................................417 Thioglycolate Bile Broth .....................................417 Thioglycolate Broth USP, Alternative .................418 Thioglycolate Gelatin Medium............................418 Thioglycolate Medium.........................................418 Thioglycolate Medium with 20% Bile ................418 Thioglycolate Medium, Brewer...........................419 Thioglycolate Medium, Brewer Modified...........419 Thioglycolate Medium, Enriched ........................419 Thioglycolate Medium without Glucose .............420 Thioglycolate Medium without Glucose and Indicator..................................................420 Thioglycolate Medium without Indicator............420 Thioglycolate Medium without Indicator-135C ..421 Thioglycolate Medium without Indicator with Hemin ....................................421 Thioglycolate Medium, USP ...............................421 Thiol Medium ......................................................422 Tinsdale Agar.......................................................422 Tissue Culture Amino Acids, HeLa 100X...........422 Tissue Culture Amino Acids, Minimal Eagle 50X .......................................422 Tissue Culture Dulbecco Solution .......................423 Tissue Culture Earle Solution ..............................423 Tissue Culture Hanks Solution ............................423 Tissue Culture Medium 199 ................................423 Tissue Culture Medium Eagle with Earle Balanced Salt Solution.........................424 Tissue Culture Medium Eagle with Hanks Balanced Salt Solution .......................424 Tissue Culture Medium Eagle, HeLa ..................425 Tissue Culture Medium Ham F10 .......................425 Tissue Culture Medium NCTC 109.....................426 Tissue Culture Medium RPMI No.1640..............427 Tissue Culture Minimal Medium Eagle...............427 Tissue Culture Minimal Medium Eagle with Earle Balanced Salts Solution ...............428 Tissue Culture Minimal Medium Eagle Spinner Modified...........................................429
Tissue Culture Tyrode Solution ...........................429 Tissue Culture Vitamins Minimal Eagle, 100X ...429 T1N0 Broth...........................................................429 T1N1 Agar ............................................................430 T1N2 Agar ............................................................430 T1N1 Broth...........................................................430 T1N3 Broth ...........................................................430 T1N6 Broth...........................................................430 T1N8 Broth...........................................................430 T1N10 Broth .........................................................430 TOC Agar.............................................................431 Todd-Hewitt Broth ...............................................431 Todd-Hewitt Broth, Modified ..............................431 Toluidine Blue DNA Agar ...................................432 Toxoplasma Medium............................................432 TPEY Agar ..........................................................432 TPGY Medium ....................................................433 Trace Elements Solution HO-LE .........................433 Transgrow Medium..............................................433 Transgrow Medium..............................................434 Transgrow Medium with Trimethoprim ..............434 Transgrow Medium without Trimethoprim .........435 Transport Medium ...............................................435 Transport Medium Stuart .....................................436 Treponema Isolation Medium ..............................436 Treponema Medium .............................................437 Treponema Medium .............................................438 Treponema Medium .............................................439 Treponema Medium .............................................440 Treponema Medium 1 ..........................................440 Treponema Medium 2 ..........................................440 Treponema Medium 3 ..........................................440 Treponema Medium, Prereduced .........................441 Trichomonas Medium ..........................................441 Trichomonas Medium No. 2 ................................441 Trichomonas Selective Medium ..........................442 Trichosel™ Broth, Modified................................442 Trimethylamine N-Oxide Medium ......................443 Triple Sugar Iron Agar.........................................443 Trypaflavin Nalidixic Acid Serum Agar..............443 Trypanosome Medium .........................................444 Tryptic Digest Broth ............................................444 Tryptic Nitrate Medium .......................................444 Tryptic Soy Agar with Sodium Chloride .............444 Tryptic Soy Fast Green Agar ...............................445 Trypticase Agar Base ...........................................445 Trypticase Agar Base with Carbohydrate ............445 Trypticase Novobiocin Broth...............................445 Trypticase Peptone Glucose Yeast Extract Broth........................................445 Trypticase Peptone Glucose Yeast Extract Broth, Buffered........................446 Trypticase Peptone Glucose Yeast Extract Broth with Trypsin ..................446 Trypticase Soy Agar ............................................446
Trypticase Soy Agar with Human Blood.............446 Trypticase Soy Agar with Lecithin and Polysorbate 80..................446 Trypticase Soy Agar, Modified............................447 Trypticase Soy Agar with Sheep Blood...............447 Trypticase Soy Agar with Sheep Blood, Formate, and Fumarate ........................................447 Trypticase Soy Agar with Sheep Blood and Gentamicin........................448 Trypticase Soy Agar with Sheep Blood, Sucrose, and Tetracycline ....................................448 Trypticase Soy Agar with Tobramycin ................448 Trypticase Soy Agar with Sheep Blood and Tween 80 ...........................449 Trypticase Soy Agar with Sheep Blood and Vacnomycin.......................449 Trypticase Soy Agar Yeast Extract ......................449 Trypticase Soy Broth with 10mM Glucose .........449 Trypticase Soy Broth without Glucose ................450 Trypticase Soy Broth with 1.5% NaCl ................450 Trypticase Soy Broth with Sheep Blood..............450 Trypticase Soy Broth with Tobramycin...............450 Trypticase Soy Broth with Tween 80...................450 Trypticase Soy Broth with Yeast Extract.............451 Trypticase Tellurite Agar Base ............................451 Tryptone Bile Glucuronide Agar, Harlequim ......451 Tryptone Bile X-glucuronide Agar, Chromocult.451 Tryptone Phosphate Broth ...................................452 Tryptone Soya Agar.............................................452 Tryptone Soya Broth............................................452 Tryptone Soya Broth with 0.1% Tween 80..........452 Tryptone Water Broth ..........................................452 Tryptone Yeast Extract Agar................................452 Tryptone Yeast Extract Agar 1.............................453 Tryptophan 1% Solution ......................................453 Tryptose Agar ......................................................453 Tryptose Agar with Citrate ..................................453 Tryptose Agar with Sheep Blood.........................453 Tryptose Agar with Thiamine..............................454 Tryptose Blood Agar ...........................................454 Tryptose Blood Agar Base with Yeast Extract ....454 Tryptose Broth .....................................................454 Tryptose Broth with Citrate .................................455 Tryptose Cycloserine Dextrose Agar...................455 Tryptose Phosphate Agar.....................................455 Tryptose Phosphate Broth....................................455 Tryptose Phosphate Broth, Modified...................455 Tryptose Sulfite Cycloserine Agar ......................456 Tryptose Sulfite Cycloserine Agar ......................456 Tryptose Sulfite Cycloserine Agar with Polymyxin and Kanamycin ...................456 Tryptose Sulfite Cycloserine Agar without Egg Yolk...........................................456 TSC Agar, Fluorocult ..........................................457 TSN Agar.............................................................457
Tween 80 Hydrolysis Broth .................................458 Tween 80 Hydrolysis Medium.............................458 TY Medium..........................................................459 TY Salt Medium ..................................................459 TYGS Medium ....................................................459 TYI-S-33 Medium ...............................................459 TYM Basal Medium, Modified 1 ........................460 TYM Basal Medium, Modified 2 ........................460 TYM Basal Medium, Modified 4 ........................460 U Agar Plates .......................................................461 U Broth ................................................................461 U9 Broth ..............................................................462 U9 Broth with Amphotericin B ...........................463 U9B Broth............................................................463 U9C Broth............................................................464 Urea Agar.............................................................464 Urea Agar Base....................................................465 Urea Broth 10B for Ureaplasma urealyticum......465 Urea Broth Base...................................................466 Urea R Broth........................................................466 Urea Semisolid Medium ......................................466 Urea Test Broth ....................................................467 Urease Test Broth.................................................467 UVM Listeria Enrichment Broth .........................468 UVM Modified Listeria Enrichment Broth .........468 V Agar..................................................................468 V-8™ Agar...........................................................468 V-8 Agar...............................................................469 Veal Infusion Agar ...............................................469 Veal Infusion Broth..............................................469 Veal Infusion Broth with Horse Serum................469 Veillonella Agar ...................................................469 Veillonella Medium..............................................470 Veillonella Medium, DSM ...................................470 Veillonella Selective Medium ..............................470 Vibrio Agar...........................................................470 Vibrio parahaemolyticus Sucrose Agar ...............471 Violet Peptone Bile Lactose Broth.......................471 Viral Transport Medium ......................................471 Vitamin B6 Blood Agar........................................471 Vitamin B6 Blood Agar with Pyridoxal-HCl .......472 VL Agar with Blood ............................................472 VL Medium..........................................................472 Vogel and Johnson Agar ......................................472 VP Medium..........................................................473 VRB Agar, Fluorocult..........................................473 VRB MUG Agar..................................................473 VRE Agar ............................................................473 VRE Agar ............................................................474 VRE Broth ...........................................................474 Wagatsuma Agar..................................................475
Wallerstein Medium.............................................475 Wickerham Broth.................................................475 Wickerham Broth.................................................476 Wickerham Broth with Raffinose ........................476 Wilkins-Chalgren Agar........................................476 Wilkins-Chalgren Anaerobe Agar .......................477 Wilkins-Chalgren Anaerobe Agar with GN Supplement ....................................477 Wilkins-Chalgren Anaerobe Agar with NS Supplement......................................477 Wilkins-Chalgren Anaerobe Broth ......................478 Wilson Blair Base ................................................478 Winge Agar..........................................................478 Wolin-Bevis Medium...........................................479 Worfel-Ferguson Agar .........................................479 Xanthine Agar......................................................479 XL Agar Base ......................................................479 XL Agar Base ......................................................480 XLD Agar ............................................................480 Xylose Lactose Tergitol 4 ....................................480 Xylose Sodium Deoxycholate Citrate Agar ...................................................481 Y1 Adrenal Cell Growth Medium .......................481 Y1 Adrenal Cell Growth Medium .......................482 Yeast Extract Agar ...............................................482 Yeast Extract Agar ...............................................483 Yeast Extract Sodium Lactate Medium ...............483 Yeast Extract Sucrose Agar .................................483 Yeast Fermentation Medium................................483 Yeast Glucose Agar .............................................484 Yeastrel Agar .......................................................484 YEPD Medium ....................................................484 Yersinia Selective Agar Base ...............................484 YI-S Medium .......................................................485 YPC Medium .......................................................485 YPNC Medium ...................................................485 Agars....................................................................487 Peptones...............................................................487 Meat and Plant Extracts .......................................488 Growth Factors ....................................................489 Selective Components .........................................491 pH Buffers ...........................................................494 Differential Components .....................................494 Preparation of Media ...........................................494 Autoclaving..........................................................494 Tyndallization ......................................................495 Inspissation ..........................................................495 Filtration ..............................................................495 Caution about Hazardous Components ...............495 Index ....................................................................497
Introduction Diagnostic Microbiology: Isolation and Identification of Pathogens The definitive diagnosis of an infectious disease is in part dependant on the detection and/or the isolation and identification of the pathogenic microorganism or the detection of antigens or antibodies specifically associated with the pathogen. Specific culture methods are used for the isolation and identification of a wide variety of pathogenic microorganisms. Traditional methods for the identification of pathogens depend on microscopic observations, phenotypic characteristics observed in culture, and metabolic changes following growth in a variety of substrates. Many differential media and selective media utilize color changes to highlight specific cultural features or substrate utilization. These growth-dependent methods provide a reliable and relatively accurate means for identifying the pathogen and diagnosing many infectious diseases. A wide range of biochemical, serological, and nucleic acid-based procedures are available for the definitive identification of microbial isolates of clinical significance. Accuracy, reliability, and speed are important factors that govern the selection of clinical identification protocols. The selection of the specific procedures to be employed for the identification of pathogenic isolates is guided by the need for presumptive or definitive identification of the organism at the family or genus and species level, based on the observation of colonial morphology, phenotypic characteristics, and other key growth characteristics on primary isolation medium. Identification of pathogenic filamentous fungi and protozoa is generally based on the morphological characteristics of the organism. Additionally, the identification of the former is based primarily on cultural and microscopic characteristics and a limited number of biochemical tests. Conventional identification schemes for bacteria and yeasts rely on the determination of a variety of biochemical features. In general, fewer than 20 biochemical tests are required to identify most clinical bacterial isolates to the species level. The primary objective is to differentiate the isolates present in the specimen using a minimal number of tests to accurately define distinct taxa.
Isolation and Culture Procedures A variety of procedures are employed for the collection, isolation, and identification of pathogenic microorganisms from different anatomical sites including tissue, body fluids, pulmonary secretions, and blood. Various procedures are used for the isolation of different types of microorganisms. Laboratory procedures are designed to screen and facilitate the recovery of etiologic agents of disease that predominate in particular clinical syndromes. When the manifestation of a disease suggests that the disease may be caused by a rare pathogen and/or routine screening fails to detect a probable causative microorganism, additional specialized isolation procedures may be required. As the clinical microbiology laboratory slowly enters into the new era of “molecular diagnostics,” the dependency on traditional culture methods involving the production and preparation of growth supporting media will continue to play an integral role in our efforts to detect and characterize both known and “new” microbial pathogens. Furthermore, the major goal of the clinical microbiology laboratory, as stated by Dr. Raymond Bartlett over twenty years ago, has not and will not change, “to provide information of maximal and epidemiological usefulness as rapidly as is consistent with acceptable accuracy and minimal cost.” The latter two criteria serve as the driving forces that account for the slow introduction and acceptance by the clinical microbiology community of methods that have been developed for either the noncultural detection or cultural confirmation of pathogenic microorganisms. Many procedures, including the more recent nucleic acid probes and gene amplification methods, remain cost prohibitive for many laboratories, lack acceptable sensitivity and/or specificity, and are not practical or adaptable for use in the service-oriented, clinical laboratory. Until such problems are resolved, microbiologists will continue to rely on the availability and utilization of a variety of media for the isolation, characterization, and identification of primary and opportunistic microbial pathogens. The selection of a specific procedure(s) to be employed for the definitive identification of a pathogen at the family or genus and species level is influenced by the information gleaned from observing colonial morphology, pigment production, and other characteristics that are observed following growth of the microorganism on either selective, differential, or general purpose media.
2
Media for the Isolation and Identification of Microorganisms from Clinical Specimens
These concepts also apply to fungi and viruses. The limited availability of practical and cost-effective detection methods requires that these microorganisms be recovered in culture before confirmation of identity can be accomplished using key morphological and biochemical characteristics, the type of cytopathic effect (CPE), or the application of culture confirmation methods such as serological, direct fluorescent antibiody, nucleic acid probes, or amplification technologies. Culture media will continue to be developed and used for the cultivation of microorganisms despite the inevitable impact that noncultural methods will have on the rapid detection of microbial pathogens and ultimately affect, in a beneficial manner, patient outcome.
Media for the Isolation and Identification of Microorganisms from Clinical Specimens The second edition of the Handbook of Media for Clinical Microbiology includes both classic and modern media used for the identification, cultivation, and maintenance of diverse bacteria described in the Manual for medically important microorganisms. Below are some of the primary media used in clinical microbiology laboratories for the isolation of pathogens.
Representative Microbiological Media that are used for Isolation and Identification of Microorganisms from Clinical Specimens
Medium
Use
Brain Heart Infusion Cultivation of a wide variety of human pathogens Medium Brilliant Green Agar
Selective cultivation of Salmonella species
Campylobacter Agar
Selective cultivation Campylobacter species
Chocolate Agar
Cultivation of a wide variety of human pathogens including Haemophilus and Neisseria species
Chopped Meat Glucose Medium
Cultivation of anaerobes
Deoxycholate Agar
Selective cultivation of Gramnegative enteric bacteria
Deoxycholate Citrate Agar
Selective cultivation of Salmonella and some Shigella species
Enterococcus Agar
Selective cultivation of enterococci
Eosin Methylene Blue Agar
Selective cultivation of Gramnegative enteric bacteria
GN Broth
Enrichment for Salmonella and Shigella species
Hektoen Enteric Agar
Selective cultivation of enteric bacteria including Shigella species
MacConkey Agar
Selective cultivation of Gramnegative enteric bacteria
of
Medium
Use
Anaerobic Blood Agar
Cultivation of a wide variety of anaerobic pathogens
Mannitol Salt Agar
Selective cultivation of Staphylococcus species
Anaerobic Kanamy- Cultivation of Bacteroides specin Vancomycin cies Laked Blood Agar
Martin–Lewis Agar
Selective cultivation of Neisseria species
New York City Agar
Selective cultivation of Neisseria and Mycoplasma species
Phenylethyl Alcohol Medium
Selective cultivation of Staphylococcus and Streptococcus species
Selenite F Broth
Enrichment species
Tetrathionate Broth
Enrichment for Salmonella and some Shigella species
Thayer Martin Agar
Selective cultivation of Neisseria species
Thioglycollate Broth
Cultivation of aerobes and anaerobes
Xylose Lysine Deoxycholate Agar
Selective cultivation of Salmonella and some Shigella species
Azide Blood Agar
Cultivation of Streptococcus pyogenes which forms small colonies and demonstrates beta hemolysis
Bacteroides Bile Esculin Agar
Cultivation of Bacteroides species
Bile Esculin Agar
Cultivation of group D streptococci including Enterococcus faecalis
Bismuth Sulfite Agar
Cultivation of Salmonella including S. typhi from faecal specimens
Blood Agar
Cultivation of many pathogens
Blood Agar with Colistin and Nalixic Acid
Selective cultivation of Grampositive bacteria
for
Salmonella
Media for the Isolation and Identification of Microorganisms from Clinical Specimens
3
Some Media and Procedures Used for the Diagnosis of Various Diseases Anatomical Site
Specimen
Culture Media
Probable Organism
Syndrome
Upper respiratory tract: throat and nasopharyngeal cultures
Sterile dacron swabs
Blood agar
Streptococcus pyogenes
Pharyngitis, rheumatic fever
Chocolate agar
Haemophilus influenzae
Epiglottitis
Neisseria gonorrhoeae
Phayingitis
Bordetella pertussis
Whooping cough
Lower respiratory tract
Central nervous system
Bordet-Gengou
Sputum, transtracheal aspirate, bronchoalveolar lavage, biopsy
Lumbar puncture for cerebro– spinal fluid
Tellurite serum agar Corynebacterium diphtheriae
Diphtheria
Blood agar
Streptococcus pneumoniae, Staphylococcus aureus
Pneumonia
Chocolate agar
Haemophilus influenzae
MacConkey’s agar
Klebsiella pneumoniae, Haemophilus influenzae
Sabouraud’s agar
Coccidioides immitis, Candida albicans
Lowenstein-Jensen
Mycobacterium tuberculosis
Tuberculosis
Liquid enrichment media
Streptococcus pneumoniae
Meningitis
Blood agar
Neisseria meningitidis
Chocolate agar
Haemophilus influenzae
Circulatory system blood
Venus puncture
Tryptic Soy BHI
Various
Septicemia
Urinary tract
Midstream catch of voided urine
Blood agar
Escherichia coli
Urinary tract infections
Cysteine lactose electrolyte-deficient agar
Klebsiella, Proteus, Pseudomonas, Salmonella
MacConkey’s agar, EMB agar
Serratia, E. coli, and other Gram-negative rods
4
Media for the Isolation and Identification of Microorganisms from Clinical Specimens Some Media and Procedures Used for the Diagnosis of Various Diseases Anatomical Site
Specimen
Culture Media
Genital tract
Urethral exudate (males) Swabs from cervix, vagina, and anal canal (females
Thayer-Martin me- Neisseria gonorrhoeae dium and chocolate agar
Gonorrhea
Intestinal tract
Stool samples
Hektoen enteric me- Salmonella-Shigella dia, xylose-lysinedesoxycholate media, brilliant green, EMB, Endo, and MacConkey’s agar
Gastroenteritis
Ears
Fluids
Blood, chocolate, and MacConkey’s agar, Gram stain
Otitis media
Skin
Swabs, aspirates, or washings from lesions
Aerobic and anaero- Clostridium tetani, bic culture techC. perfringens niques
References Atlas of the Clinical Microbiology of Infectious Diseases, Volume 1: Bacterial Agents. 2003. Bottone, E.J. Parthenon Pub. Group, New York. Atlas of the Clinical Microbiology of Infectious Diseases, Volume 2: Viral, Fungal, and Parasitic Agents, 2006. Bottone, E.J. Parthenon Pub. Group, New York. Biohazardous Bloodborne and Airborne Pathogens: A Guide for Clinical and Laboratory Safety. 2004. Langerman, N. Lewis Pub., Boca Raton, FL. Clinical Bacteriology. 2003. Struthers, J.K. and R.P. Westran. ASM Press, Washington DC. Clinical Microbiology Procedures Handbook. 2004. Isenberg, H.D., L. Clarke, P. Della-Latta, G.A. Denys, S.D. Douglas, L.S. Garcia, K.C. Hazen, J.F. Hindler, and S.G. Jenkins. ASM Press, Washington DC. Clinical Mycology. 2003. Anaissie, E.J., M.R. McGinnis, and M.A. Pfaller. Churchill Livingston, New York.
Probable Organism
Haemonpilus influenzae
Syndrome
Tetanus Gas gangrene
P.C. Schreckenberger, and W.C. Winn, Jr., eds. J.B. Lippincott Co., Philadelphia, PA. Diagnostic Microbiology. 1990. Finegold, S.M. and W.J. Martin. C.V. Mosby Co., St. Louis, MO. Difco & BBL Manual: Dehydrated Culture Media and Reagents for Microbiology. 2003. Becton, Dickinson and Co., Sparks, MD. Manual of Clinical Microbiology, eighth edition. 2003. Murray, P.R., E.J.Baron. J.H. Jorgensen, M.A. Pfaller, and R.H. Yolken. ASM Press, Washington, DC. Media for Isolation–Cultivation–Identification– Maintenance of Medical Bacteria. 1985. McFaddin, J.F. Williams and Wilkins, Baltimore, MD. Pocket Guide to Clinical Microbiology. 2004. Murray, P. R. ASM Press, Washington DC. Practical Guide to Clinical Virology. 2002. Haaheim L.R., J.R. Pattison, and R.J. Whitley. John Wiley & Sons, Chichester, UK.
Clinical Mycology. 2003. Dismukes, W.E., P.G. Pappas, and J.D. Sobel. Oxford University Press, New York.
Principles and Practice of Clinical Virology. 2004. Zuckerman, A.J., J.E. Banatvala, P. Griffiths, J.R. Pattison, and B. Schoub. John Wiley & Sons, Chichester, UK.
Color Atlas and Textbook of Diagnostic Microbiology. 1992. Koneman, E.W., S.D. Allen, W.M. Janda,
Textbook of Diagnostic Microbiology. Mahon, C. Saunders, Philadelphia.
2000.
A 3B Agar
A 3 Agar Composition per 202.4mL: Agar base .................................................... 140.0mL Supplement solution ..................................... 62.4mL pH 6.0 ± 0.2 at 25°C
Agar Base: Composition per liter: Pancreatic digest of casein................................17.0g Ionagar no. 2 .......................................................7.5g NaCl ....................................................................5.0g Papaic digest of soybean meal ............................3.0g K2HPO4 ...............................................................2.5g Glucose ...............................................................2.5g
Source: Ionagar no. 2 is available from Oxoid Unipath.
Phenol Red Solution: Composition per 10.0mL: Phenol Red..........................................................0.1g
Preparation of Phenol Red Solution: Add Phenol Red to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Aseptically combine 140.0mL of cooled, sterile agar base and 62.4mL of sterile supplement solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation of Ureaplasma urealyticum from urine for the detction of urogenital infections. Also used for the cultivation of other Ureaplasma species.
Preparation of Agar Base: Add components, except agar, to distilled/deionized water and bring volume to 1.0L. Adjust pH to 5.5. Add agar. Mix thoroughly. Gently heat and bring to boiling. Distribute into screw-capped bottles in 140.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Supplement Solution: Composition per 62.4mL:
5
A 3B Agar Composition per 101.5mL: Agar base ...................................................... 80.0mL Supplement solution ..................................... 21.5mL pH 6.0 ± 0.2 at 25°C
Agar Base: Composition per liter:
Horse serum-urea solution ............................ 40.0mL Fresh yeast extract solution........................... 20.0mL Penicillin solution ........................................... 2.0mL Phenol Red solution ........................................ 0.4mL
Pancreatic digest of casein................................17.0g Ionagar no. 2 .......................................................7.5g NaCl....................................................................5.0g Papaic digest of soybean meal............................3.0g K2HPO4...............................................................2.5g Glucose ...............................................................2.5g
Preparation of Supplement Solution: Asepti-
Source: Ionagar no. 2 is available from Oxoid Uni-
cally combine components. Mix thoroughly.
Horse Serum-Urea Solution: Composition per 40.0mL:
path.
Preparation of Agar Base: Add components, ex-
Add urea to 40.0mL of horse serum. Mix thoroughly. Filter sterilize.
cept agar, to distilled/deionized water and bring volume to 1.0L. Adjust pH to 5.5. Add agar. Mix thoroughly. Gently heat and bring to boiling. Distribute into screw-capped bottles in 80.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Fresh Yeast Extract Solution: Composition:
Supplement Solution: Composition per 21.5mL:
Baker’s yeast, live, pressed, starch-free............25.0g
Horse serum-urea solution............................ 20.0mL Penicillin solution ........................................... 1.0mL L-Cysteine·HCl·H2O solution ......................... 0.5mL
Urea.....................................................................0.2g Horse serum, unheated.................................. 40.0mL
Preparation of Horse Serum-Urea Solution:
Preparation of Fresh Yeast Extract Solution: Add the live Baker’s yeast to 100.0mL of distilled/ deionized water. Autoclave for 90 min at 15 psi pressure–121°C. Allow to stand. Remove supernatant solution. Adjust pH to 6.6–6.8. Filter sterilize.
Penicillin Solution: Composition per 10.0mL:
Preparation of Supplement Solution: Aseptically combine components. Mix thoroughly.
Horse Serum-Urea Solution: Composition per 40.0mL:
Penicillin G .............................................1,000,000U
Urea.....................................................................0.2g Horse serum, unheated.................................. 40.0mL
Preparation of Penicillin Solution: Add peni-
Preparation of Horse Serum-Urea Solution:
cillin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Add urea to 40.0mL of horse serum. Mix thoroughly. Filter sterilize.
6
A 7 Agar
Penicillin Solution: Composition per 10.0mL:
Fresh Yeast Extract Solution: Composition per 100.0mL:
Penicillin G .............................................1,000,000U
Baker’s yeast, live, pressed, starch-free............25.0g
Preparation of Penicillin Solution: Add peni-
Preparation of Fresh Yeast Extract Solution: Add the live Baker’s yeast to 100.0mL of distilled/ deionized water. Autoclave for 90 min at 15 psi pressure–121°C. Allow to stand. Remove supernatant solution. Adjust pH to 6.6–6.8. Filter sterilize.
cillin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. L-Cysteine·HCl·H2O
Solution: Composition per 10.0mL: L-Cysteine·HCl·H2O............................................0.2g
Preparation of L-Cysteine·HCl·H2O Solution: Add L-cysteine·HCl·H2O to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Aseptically combine
Penicillin Solution: Composition per 10.0mL: Penicillin G ............................................. 1,000,000U
Preparation of Penicillin Solution: Add penicillin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
80.0mL of cooled, sterile agar base and 21.5mL of sterile supplement solution. Mix thoroughly.
CVA Enrichment: Composition per liter:
Use: For the cultivation of Ureaplasma urealyticum from urine for the detction of urogenital infections. Also used for the cultivation of other Ureaplasma species.
Glucose ...........................................................100.0g L-Cysteine·HCl·H2O..........................................25.9g L-Glutamine ......................................................10.0g L-Cystine·2HCl ...................................................1.0g Adenine...............................................................1.0g Nicotinamide adenine dinucleotide ..................0.25g Cocarboxylase.....................................................0.1g Guanine·HCl .....................................................0.03g Fe(NO3)3 ...........................................................0.02g Vitamin B12 .......................................................0.01g p-Aminobenzoic acid......................................0.013g Thiamine·HCl ..................................................3.0mg
A 7 Agar (Shepard’s Differential Agar) Composition per 205.7mL: Agar base .................................................... 160.0mL Supplement solution ..................................... 45.7mL pH 6.0 ± 0.2 at 25°C
Agar Base: Composition per 165.0mL: Pancreatic digest of casein................................2.72g Agar ....................................................................2.1g NaCl ....................................................................0.8g Papaic digest of soybean meal ..........................0.48g K2HPO4 ...............................................................0.4g Glucose ...............................................................0.4g MnSO4·H2O ......................................................0.15g
Preparation of Agar Base: Add components, except agar, to distilled/deionized water and bring volume to 165.0mL. Adjust pH to 5.5. Add agar. Mix thoroughly. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C.
Supplement Solution: Composition per 45.72mL: Horse serum, unheated.................................. 40.0mL Fresh yeast extract solution............................. 2.0mL Penicillin solution ........................................... 2.0mL CVA enrichment.............................................. 1.0mL L-Cysteine·HCl·H2O solution.......................... 0.5mL Urea solution................................................. 0.22mL
Preparation of Supplement Solution: Aseptically combine components. Mix thoroughly.
Preparation of CVA Enrichment: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize. L-Cysteine·HCl·H2O
Solution: Composition per 10.0mL: L-Cysteine·HCl·H2O............................................0.4g
Preparation of L-Cysteine·HCl·H2O Solution: Add L-cysteine·HCl·H2O solution to distilled/
deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Urea Solution: Composition per 10.0mL: Urea, ultrapure ....................................................1.0g
Preparation of Urea Solution: Add urea to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Aseptically combine 160.0mL of cooled, sterile agar base and 45.9mL of sterile supplement solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation and differentiation of Ureaplasma urealyticum from urine based on its ability to produce ammonia from urea for the detction of uro-
A 7B Agar genital infections. Bacteria that produce ammonia appear as golden to dark brown colonies. Also used for the cultivation of other Ureaplasma species.
A 7 Agar, Modified Composition per 205.7mL: Agar base .................................................... 160.0mL Supplement solution ..................................... 45.7mL pH 6.0 ± 0.2 at 25°C
Agar Base: Composition per 165.0mL: Agar ..................................................................10.0g Pancreatic digest of casein................................2.72g NaCl ....................................................................0.8g Papaic digest of soybean meal ..........................0.48g K2HPO4 ...............................................................0.4g Glucose ...............................................................0.4g MnSO4·H2O ......................................................0.15g
Preparation of Agar Base: Add components, except agar, to distilled/deionized water and bring volume to 165.0mL. Adjust pH to 5.5. Add agar. Mix thoroughly. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C.
Supplement Solution: Composition per 45.72mL: Horse serum, unheated.................................. 40.0mL Fresh yeast extract solution............................. 2.0mL Penicillin solution ........................................... 2.0mL CVA enrichment.............................................. 1.0mL L-Cysteine·HCl·H2O solution.......................... 0.5mL Urea solution................................................. 0.22mL
Preparation of Supplement Solution: Aseptically combine components. Mix thoroughly.
Fresh Yeast Extract Solution: Composition per 100.0mL: Baker’s yeast, live, pressed, starch-free............25.0g
Preparation of Fresh Yeast Extract Solution: Add the live Baker’s yeast to 100.0mL of distilled/ deionized water. Autoclave for 90 min at 15 psi pressure–121°C. Allow to stand. Remove supernatant solution. Adjust pH to 6.6–6.8. Filter sterilize. Penicillin Solution: Composition per 10.0mL: Penicillin G .............................................1,000,000U
Preparation of Penicillin Solution: Add penicillin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
CVA Enrichment: Composition per liter: Glucose ...........................................................100.0g L-Cysteine·HCl·H2O..........................................25.9g
7
L-Glutamine
......................................................10.0g ...................................................1.0g Adenine...............................................................1.0g Nicotinamide adenine dinucleotide ..................0.25g Cocarboxylase.....................................................0.1g Guanine·HCl .....................................................0.03g Fe(NO3)3 ...........................................................0.02g p-Aminobenzoic acid......................................0.013g Vitamin B12 .......................................................0.01g Thiamine·HCl ..................................................3.0mg L-Cystine·2HCl
Preparation of CVA Enrichment: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize. L-Cysteine·HCl·H2O
Solution: Composition per 10.0mL: L-Cysteine·HCl·H2O............................................0.4g
Preparation of L-Cysteine·HCl·H2O Solution: Add L-cysteine·HCl·H2O solution to distilled/
deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Urea Solution: Composition per 10.0mL: Urea, ultrapure ....................................................1.0g
Preparation of Urea Solution: Add urea to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Aseptically combine 160.0mL of cooled, sterile agar base and 45.9mL of sterile supplement solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation and differentiation of Ureaplasma urealyticum from urine based on its ability to produce ammonia from urea for the detction of urogenital infections. Bacteria that produce ammonia appear as golden to dark brown colonies. Also used for the cultivation of other Ureaplasma species.
A 7B Agar Composition per 205.7mL: Agar base .................................................... 160.0mL Supplement solution ..................................... 45.7mL pH 6.0 ± 0.2 at 25°C
Agar Base: Composition per 165.0mL: Pancreatic digest of casein................................2.72g Agar ....................................................................2.1g NaCl....................................................................0.8g Papaic digest of soybean meal..........................0.48g K2HPO4...............................................................0.4g Glucose ...............................................................0.4g Putrescine·2HCl ................................................0.33g MnSO4·H2O ......................................................0.15g
8
A 8B Agar
Preparation of Agar Base: Add components, except agar, to distilled/deionized water and bring volume to 165.0mL. Adjust pH to 5.5. Add agar. Mix thoroughly. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C.
Supplement Solution: Composition per 45.72mL: Horse serum, unheated.................................. 40.0mL Fresh yeast extract solution............................. 2.0mL Penicillin solution ........................................... 2.0mL CVA enrichment.............................................. 1.0mL L-Cysteine·HCl·H2O solution.......................... 0.5mL Urea solution................................................. 0.22mL
deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Urea Solution: Composition per 10.0mL: Urea, ultrapure ....................................................1.0g
Preparation of Urea Solution: Add urea to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Aseptically combine 160.0mL of cooled, sterile agar base and 45.9mL of sterile supplement solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Preparation of Supplement Solution: Asepti-
Use: For the cultivation and differentiation of Urea-
cally combine components. Mix thoroughly.
plasma urealyticum from urine based on its ability to produce ammonia from urea for the detction of urogenital infections. Bacteria that produce ammonia appear as golden to dark brown colonies. Also used for the cultivation of other Ureaplasma species.
Fresh Yeast Extract Solution: Composition per 100.0mL: Baker’s yeast, live, pressed, starch-free............25.0g
Preparation of Fresh Yeast Extract Solution: Add the live Baker’s yeast to 100.0mL of distilled/ deionized water. Autoclave for 90 min at 15 psi pressure–121°C. Allow to stand. Remove supernatant solution. Adjust pH to 6.6–6.8. Filter sterilize. Penicillin Solution: Composition per 10.0mL: Penicillin G .............................................1,000,000U
Preparation of Penicillin Solution: Add penicillin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
CVA Enrichment: Composition per liter: Glucose ...........................................................100.0g L-Cysteine·HCl·H2O..........................................25.9g L-Glutamine.......................................................10.0g L-Cystine·2HCl....................................................1.0g Adenine...............................................................1.0g Nicotinamide adenine dinucleotide ..................0.25g Cocarboxylase.....................................................0.1g Guanine·HCl .....................................................0.03g Fe(NO3)3 ...........................................................0.02g p-Aminobenzoic acid......................................0.013g Vitamin B12 .......................................................0.01g Thiamine·HCl ..................................................3.0mg
Preparation of CVA Enrichment: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize. L-Cysteine·HCl·H2O
Solution: Composition per 10.0mL: L-Cysteine·HCl·H2O............................................0.4g
Preparation of L-Cysteine·HCl·H2O Solution: Add L-cysteine·HCl·H2O solution to distilled/
A 8B Agar Composition per 84.6mL: Agar base ...................................................... 80.0mL Supplement solution ....................................... 4.6mL pH 6.0 ± 0.2 at 25°C
Agar Base: Composition per 165.0mL: Pancreatic digest of casein................................2.72g Agar ....................................................................2.1g NaCl....................................................................0.8g Papaic digest of soybean meal..........................0.48g K2HPO4...............................................................0.4g Glucose ...............................................................0.4g MnSO4·H2O ......................................................0.15g CaCl2·2H2O ......................................................0.03g Putrescine·2HCl .............................................34.0mg
Preparation of Agar Base: Add components, except agar, to distilled/deionized water and bring volume to 165.0mL. Adjust pH to 5.5. Add agar. Mix thoroughly. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C.
Supplement Solution: Composition per 4.6mL: Horse serum, unheated.................................... 1.0mL Fresh yeast extract solution ............................ 1.0mL Penicillin solution ........................................... 1.0mL Urea solution................................................... 1.0mL L-Cysteine·HCl·H2O solution ......................... 0.5mL GHL tripeptide solution.................................. 0.1mL
Preparation of Supplement Solution: Aseptically combine components. Mix thoroughly.
Abeyta-Hunt Bark Agar
9
Fresh Yeast Extract Solution: Composition per 100.0mL:
Source: This medium is available as a premixed
Baker’s yeast, live, pressed, starch-free............25.0g
Preparation of Medium: Add components to
Preparation of Fresh Yeast Extract Solution:
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into test tubes containing an inverted Durham tube. Autoclave for 10 min at 15 psi pressure–121°C.
Add the live Baker’s yeast to 100.0mL of distilled/ deionized water. Autoclave for 90 min at 15 psi pressure–121°C. Allow to stand. Remove supernatant solution. Adjust pH to 6.6–6.8. Filter sterilize.
Penicillin Solution: Composition per 10.0mL: Penicillin G .............................................1,000,000U
Preparation of Penicillin Solution: Add penicillin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
GHL Tripeptide Solution: Composition per 10.0mL: GHL (Glycyl-L-histidyl-L-lysine acetate) tripeptide .........................................0.2g
Preparation of GHL Tripeptide Solution:
powder from BD Diagnostic Systems.
Use: For the detection of fecal coliforms by a mostprobable-number (MPN) method. Multiple dilutions of samples (3, 5, or 10 replicates per dilution) are added to tubes containing A 1 broth. After incubation, test tubes with gas accumulation in the Durham tubes are scored positive and those with no gas as negative. An MPN table is consulted to determine the most probable number of fecal coliforms.
Abeyta-Hunt Bark Agar Composition per 1016.0mL:
deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Beef heart, infusion from................................500.0g Agar ..................................................................15.0g Tryptose ............................................................10.0g NaCl....................................................................5.0g Yeast extract........................................................2.0g Horse blood, lysed ........................................ 50.0mL Amphotericin B solution................................. 4.0mL Cefoperazone solution .................................... 4.0mL Rifampicin solution ........................................ 4.0mL Ferrous sulfate pyruvate metabisulfite solution ............................... 4.0mL pH 7.4 ± 0.2 at 25°C
Urea Solution: Composition per 10.0mL:
Amphotericin B Solution: Composition per 100.0mL:
Add GHL (Glycyl-L-histidyl-L-lysine acetate) tripeptide to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. L-Cysteine·HCl·H2O
Solution: Composition per 10.0mL: L-Cysteine·HCl·H2O............................................0.4g
Preparation of L-Cysteine·HCl·H2O Solution: Add L-cysteine·HCl·H2O solution to distilled/
Urea, ultrapure ....................................................1.0g
Preparation of Urea Solution: Add urea to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Aseptically combine
Amphotericin B ................................................0.05g
Preparation of Amphotericin B Solution: Add Amphotericin B to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
80.0mL of cooled, sterile agar base and 4.6mL of sterile supplement solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Cefoperazone Solution: Composition per 100.0mL:
Use: For the cultivation of Ureaplasma urealyticum
Preparation of Cefoperazone Solution: Add
from urine. Also used for the cultivation of other Ureaplasma species.
A 1 Broth Composition per liter: Pancreatic digest of casein................................20.0g Lactose ................................................................5.0g NaCl ....................................................................5.0g Salicin .................................................................0.5g Triton™ X-100 ............................................... 1.0mL pH 6.9 ± 0.1 at 25°C
Sodium cefoperazone........................................0.08g sodium cefoperazone to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Rifampicin Solution: Composition per 100.0mL: Rifampicin ........................................................0.25g
Preparation of Rifampicin Solution: Add rifampicin to 70.0mL ethanol. Mix thoroughly. Add distilled/deionized water to bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
10
ABY Agar
Ferrous Sulfate, Pyruvate, Metabisulfite Solution: Composition per 100.0mL: FeSO4 ................................................................6.25g Na-pyruvate ......................................................6.25g Na-metabisulfite................................................6.25g
Preparation of Ferrous Sulfate, Pyruvate, Metabisulfite Solution: Add Na-pyruvate to 20mL distilled/deionized water. Mix thoroughly. Add Na-metabisulfite and FeSO4. Bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except cefoperazone solution, amphotericin B solution, rifampicin solution, ferrous sulfate pyruvate metabisulfide solution, and horse blood, to distilled/ deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C. Aseptically add 4.0mL cefoperazone solution, 4.0mL amphotericin B solution, 4.0mL rifampicin solution, 4.0mL ferrous sulfate pyruvate metabisulfide solution, and 50.0mL lysed horse blood. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
brown to black colonies with no pigment diffusion and no sheen, whereas Candida tropicalis appears as dark brown colonies with black centers, black pigment diffusion, and a sheen.
AC Agar (AC Medium) Composition per liter: Proteose peptone no. 3......................................20.0g Glucose ...............................................................5.0g Beef extract.........................................................3.0g Yeast extract........................................................3.0g Malt extract.........................................................3.0g Ascorbic acid ......................................................0.2g Agar ....................................................................1.0g pH 7.2 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to
Use: For the isolation and cultivation of Campylo-
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
bacter spp.
Use: For the cultivation and isolation of anaerobes,
ABY Agar (Acid Bismuth Yeast Agar)
microaerophiles, and aerobes. Recommended for the sterility testing of solutions and other materials not containing mercurial preservatives.
Composition per liter: Agar ..................................................................20.0g Glucose .............................................................20.0g Bi2(SO3)2 .............................................................8.0g (NH4)2SO4...........................................................3.0g KH2PO4 ...............................................................3.0g MgSO4·7H2O ....................................................0.25g CaCl2·2H2O.......................................................0.25g Biotin ............................................................. 10.0µg pH 7.2 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Cool tubes in a slanted position.
Use: For the selective isolation and differentiation of Candida albicans from other Candida species. Candida albicans and Candida tropicalis colonies appear as smooth, brownish-black round colonies. Other Candida species are differentially pigmented or produce diffusible pigments. Usually used in conjunction with BiGGY agar to differentiate further Candida; on BiGGY agar, Candida albicans appears as
AC Broth Composition per liter: Proteose peptone no. 3......................................20.0g Glucose ...............................................................5.0g Beef extract.........................................................3.0g Yeast extract........................................................3.0g Malt extract.........................................................3.0g Ascorbic acid ......................................................0.2g pH 7.2 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation and isolation of a wide variety of microorganisms, including anaerobes, microaerophiles, and aerobes. Recommended for the sterility testing of solutions and other materials not containing mercurial preservatives.
Acetamide Broth
Acanthamoeba Medium Composition per liter: Proteose peptone ...............................................15.0g Glucose .............................................................15.0g KH2PO4 ...............................................................0.3g L-Methionine..................................................14.9mg Thiamine ..........................................................1.0mg Biotin ...............................................................0.2mg Vitamin B12 ...................................................... 1.0µg Salt solution .................................................... 1.0mL pH 5.5 ± 0.2 at 25°C
Salt Solution: Composition per 100.0mL: MgSO4·7H2O ................................................... 2.46g CaCl2·2H2O.......................................................0.15g FeCl3 .................................................................0.02g
Preparation of Salt Solution: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 5.5. Filter through Whatman paper to remove particles. Distribute into screw-capped tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of Acanthamoeba species.
ACC Medium Composition per liter: Proteose peptone ...............................................20.0g Agar ..................................................................12.0g Glycerol ..............................................................1.5g K2SO4..................................................................1.5g MgSO4·7H2O ......................................................1.5g Antibiotic solution ........................................ 10.0mL pH 7.2 ± 0.2 at 25°C
Antibiotic Solution: Composition per 10.0mL:
11
Use: For the selective isolation and cultivation of fluorescent Pseudomonas species.
Acetamide Agar Composition per liter: Agar ..................................................................15.0g Acetamide .........................................................10.0g NaCl....................................................................5.0g K2HPO4...............................................................1.0g NH4H2PO4 ..........................................................1.0g MgSO4·7H2O ......................................................0.2g Bromthymol Blue .............................................0.08g pH 6.9 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Adjust pH. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Cool tubes in a slanted position to produce a long slant.
Use: For the differentiation of nonfermentative Gram-negative bacteria, especially Pseudomonas aeruginosa. Bacteria that deamidate acetamide turn the medium blue.
Acetamide Agar Composition per liter: Agar ..................................................................15.0g Acetamide .........................................................10.0g NaCl....................................................................5.0g K2HPO4.............................................................1.39g KH2PO4.............................................................0.73g MgSO4·7H2O ......................................................0.5g Phenol Red......................................................0.012g pH 6.9 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to
Cycloheximide ................................................0.075g Ampicillin .........................................................0.05g Chloramphenicol...........................................0.0125g
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Adjust pH. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Cool tubes in a slanted position to produce a long slant.
Preparation of Antibiotic Solution: Add com-
Use: For the differentiation of nonfermentative
ponents to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except antibiotic solution, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile antibiotic solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Gram-negative bacteria, especially Pseudomonas aeruginosa. Bacteria that deamidate acetamide turn the medium blue.
Acetamide Broth Composition per liter: Acetamide .........................................................10.0g NaCl....................................................................5.0g K2HPO4.............................................................1.39g
12
Acetamide Cetrimide Glycerol Mannitol Selective Medium
KH2PO4 .............................................................0.73g MgSO4·7H2O ......................................................0.5g Phenol Red......................................................0.012g pH 6.9 ± 0.2 at 25°C
MgSO4·7H2O solution.................................... 2.4mL Trace elements solution .................................. 1.0mL
Preparation of Medium: Add components to
CsC12 ..............................................................16.84g
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the differentiation of nonfermentative Gram-negative bacteria, especially Pseudomonas aeruginosa. Bacteria that deamidate acetamide turn the broth purplish red.
CsCl2 Solution: Composition per 100.0mL: Preparation of CsCl2 Solution: Add CsC12 to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Acetamide Solution: Composition per 100.0mL: Acetamide .........................................................5.91g
Acetamide Cetrimide Glycerol Mannitol Selective Medium Composition per liter: Agar ..................................................................15.0g K2SO4................................................................10.0g D-Mannitol ..........................................................5.0g MgCl2·6H2O .......................................................1.4g Cetrimide ............................................................0.3g Peptone................................................................0.2g Acetamide solution ..................................... 100.0mL Glycerol .......................................................... 5.0mL pH 7.0 ± 0.2 at 25°C
Acetamide Solution: Composition per 100.0mL: Acetamide .........................................................10.0g Phenol Red......................................................0.012g
Preparation of Acetamide Solution: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except acetamide solution, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Adjust pH to 7.0. Gently heat and bring to boiling. Autoclave for 20 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile acetamide solution. Mix thoroughly. Pour into sterile Petri dishes.
Use: For the cultivation of Pseudomonas aeruginosa, Pseudomonas fluorescens, Pseudomonas putida, Pseudomonas alcaligenes, Pseudomonas cepacia, and Pseudomonas pseudoalcaligenes.
Acetamide Medium Composition per liter: Agar, noble........................................................20.0g Glucose .............................................................20.0g KH2PO4 ............................................................15.0g CsC12 solution............................................... 12.5mL Acetamide solution ....................................... 10.0mL CaCl2·2H2O solution ...................................... 4.1mL
Preparation of Acetamide Solution: Add acetamide to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C.
CaCl2·2H2O Solution: Composition per 100.0mL: CaCl2·2H2O ......................................................14.7g
Preparation of CaCl2·2H2O Solution: Add CaCl2·2H2O to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. MgSO4·7H2O Solution: Composition per 100.0mL: MgSO4·7H2O..................................................24.65g
Preparation of MgSO4·7H2O Solution: Add MgSO4·7H2O to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Trace Elements Solution: Composition per liter: FeSO4·7H2O .......................................................5.0g CoCl2·6H2O........................................................3.7g MnSO4·1H2O......................................................1.6g ZnSO4·7H2O.......................................................1.4g
Preparation of Trace Elements Solution: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly.
Preparation of Medium: Add components, except CsC12 solution, acetamide solution, CaCl2·2H2O solution, and MgSO4·7H2O solution, to distilled/ deionized water and bring volume to 971.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Aseptically add 12.5mL of sterile CsC12 solution, 10.0mL of sterile acetamide solution, 4.1mL of sterile CaCl2·2H2O solution, and 2.4mL of sterile MgSO4·7H2O solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Acetobacteroides glycinophilus Medium Use: For the cultivation and maintenance of Trichoderma longibrachiatum.
Acetamide Medium Composition per liter: Stock basal solution .................................... 400.0mL Stock acetamide solution ............................ 100.0mL pH 6.9 ± 0.2 at 25°C
Stock Basal Solution: Composition per 400.0mL: Agar ....................................................................0.5g KH2PO4 solution, 0.5M ................................ 14.0mL K2HPO4 solution, 0.5M .................................. 6.0mL
Preparation of Stock Basal Solution: Add components, except PR-CV solution, to distilled/ deionized water and bring volume to 400.0mL. Mix thoroughly. Gently heat and bring to boiling with agitation to dissolve agar. Add 1.0mL PR-CV solution.
PR-CV Solution: Composition per 200.0mL: Phenol Red..........................................................2.0g Crystal Violet ......................................................0.2g
Preparation of PR-CV Solution: Add components to distilled/deionized water and bring volume to 200.0mL. Mix thoroughly. Add 5N NaOH while stirring until components are dissolved.
Stock Acetamide Solution: Composition per 100.0mL: Acetamide ...........................................................1.0g
Preparation of Stock Acetamide Solution: Add acetamide to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Store over methylene chloride in a screw capped container. Can be stored indefinitely at room temperature.
Preparation of Medium: Combine 400.0mL
13
MgSO4·7H2O ......................................................0.2g Bromthymol Blue .............................................0.08g pH 6.8 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to cold distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes to produce a 1 cm butt and 30 cm slant. Autoclave for 15 min at 15 psi pressure– 121°C. Cool tubes in a slanted position.
Use: For the differentiation of Shigella species from Escherichia coli and also for the differentiation of nonfermenting Gram-negative bacteria. Bacteria that can utilize acetate as the sole carbon source turn the medium blue.
Acetobacteroides glycinophilus Medium Composition per 1020.0mL: Na2HPO4 .............................................................5.8g KH2PO4...............................................................3.0g NH4Cl .................................................................1.0g MgCl2·6H2O .......................................................0.2g Resazurin .........................................................1.0mg CaCl2·2H2O ......................................................0.13g Trace elements solution ................................ 10.0mL Vitamin solution.............................................. 5.0mL Yeast extract solution...................................... 5.0mL Glycine solution.............................................. 5.0mL NaHCO3 solution ............................................ 5.0mL Na2S·9H2O solution........................................ 5.0mL pH 7.2–7.4 at 25°C
Trace Elements Solution: Composition per liter:
Composition per liter:
Nitrilotriacetic acid .............................................2.8g NaCl....................................................................1.0g FeCl3·4H2O .........................................................0.2g CoCl2·6H2O ......................................................0.17g CaCl2·2H2O ........................................................0.1g MnCl2·4H2O .......................................................0.1g ZnCl2 ...................................................................0.1g NiCl2·6H2O .....................................................0.026g CuCl2 ................................................................0.02g Na2SeO·5H2O ...................................................0.02g H3BO3 ...............................................................0.01g Na2MoO·2H2O..................................................0.01g
Agar ..................................................................20.0g NaCl ....................................................................5.0g Sodium acetate....................................................2.0g (NH4)H2PO4 ........................................................1.0g K2HPO4 ...............................................................1.0g
Preparation of Trace Elements Solution: Add nitrilotriacetic acid to 500.0mL of distilled/deionized water. Dissolve by adjusting pH to 6.5 with KOH. Add distilled/deionized water to 1.0L. Add remaining components. Mix thoroughly.
stock basal solution and 100.0mL stock acetamide solution. Mix thoroughly. Distribute into tubes or flasks. Steam for 10 min at 100°C. Cool.
Use: For the differentiation of nonfermentative Gram-negative bacteria, especially Pseudomonas aeruginosa.
Acetate Differential Agar (Sodium Acetate Agar) (Simmons’ Citrate Agar, Modified)
14
Achromobacter Choline Medium
Vitamin Solution: Composition per liter: Pyridoxine·HCl ..............................................10.0mg Calcium DL-pantothenate.................................5.0mg Lipoic acid .......................................................5.0mg Nicotinic acid ...................................................5.0mg p-Aminobenzoic acid.......................................5.0mg Riboflavin ........................................................5.0mg Thiamine·HCl ..................................................5.0mg Biotin ...............................................................2.0mg Folic acid..........................................................2.0mg Vitamin B12 ......................................................0.1mg
Preparation of Vitamin Solution: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly.
Yeast Extract Solution: Composition per 5.0mL: Yeast extract........................................................0.5g
Preparation of Yeast Extract Solution: Add yeast extract to distilled/deionized water and bring volume to 5.0mL. Mix thoroughly. Sparge under 100% N2 gas for 3 min. Autoclave for 15 min at 15 psi pressure–121°C. Store under N2 gas.
just pH to 7.2–7.4 with NaOH. Mix thoroughly. Gently heat and bring to boiling. Boil for a few minutes. Allow to cool to room temperature under 100% N2. Distribute into tubes or flasks under 100% N2. Autoclave for 15 min at 15 psi pressure–121°C. Cool to room temperature. Before inoculation, aseptically and anaerobically add yeast extract solution, glycine solution, NaHCO3 solution, and Na2S·9H2O solution.
Use: For the cultivation and maintenance of Acetobacteroides glycinophilus.
Achromobacter Choline Medium Composition per liter: NaCl..................................................................30.0g Agar ..................................................................18.0g Choline chloride..................................................5.0g K2HPO4...............................................................1.0g MgSO4·7H2O ......................................................0.5g FeSO4·7H2O......................................................0.01g
Preparation of Medium: Add components to
Glycine................................................................1.5g
distilled/deionized water and bring volume to 1.0L. Mix well and warm gently until dissolved. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes.
Preparation of Glycine Solution: Add glycine
Use: For the cultivation and maintenance of Achro-
Glycine Solution: Composition per 5.0mL:
to distilled/deionized water and bring volume to 5.0mL. Mix thoroughly. Sparge under 100% N2 gas for 3 min. Autoclave for 15 min at 15 psi pressure– 121°C. Store under N2 gas.
NaHCO3 Solution: Composition per 5.0mL: NaHCO3 ..............................................................0.5g
mobacter cholinophagum and other bacteria that can utilize choline as a carbon source.
Achromobacter Choline Medium, Modified Composition per liter:
Na2S·9H2O Solution: Composition per 5.0mL:
NaCl..................................................................30.0g Agar ..................................................................15.0g Choline chloride..................................................5.0g K2HPO4...............................................................1.0g MgSO4·7H2O ......................................................1.0g FeSO4·7H2O....................................................0.018g pH 7.4 ± 0.2 at 25°C
Na2S·9H2O..........................................................0.5g
Preparation of Medium: Add agar, MgSO4·7H2O,
Preparation of NaHCO3 Solution: Add
NaHCO3 to distilled/deionized water and bring volume to 5.0mL. Mix thoroughly. Sparge under 100% N2 gas for 3 min. Autoclave for 15 min at 15 psi pressure–121°C. Store under N2 gas.
Preparation of Na2S·9H2O Solution: Add
Na2S·9H2O solution to distilled/deionized water and bring volume to 5.0mL. Mix thoroughly. Sparge under 100% N2 gas for 3 min. Autoclave for 15 min at 15 psi pressure–121°C. Store under N2 gas.
Preparation of Medium: Add components, except yeast extract solution, glycine solution, NaHCO3 solution, and Na2S·9H2O solution, to distilled/deionized water and bring volume to 1.0L. Ad-
and FeSO4·7H2O to 500.0mL distilled/deionized water. Mix thoroughly. Bring volume to 1.0L with distilled/deionized water. Gently heat and bring to boiling. Add choline chloride. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of Achromobacter cholinophagum.
Actidione® Agar
Achromobacter Medium (ATCC Medium 457)
15
or flasks. Autoclave for 15 min at 15 psi pressure– 121°C with tubes in an upright position.
Composition per liter:
Use: For the cultivation and maintenance of Myco-
K2HPO4 .............................................................7.32g Ammonium tartrate.............................................4.6g KH2PO4 .............................................................1.09g MgSO4·7H2O ....................................................0.04g FeSO4·7H2O......................................................0.04g CaCl2·2H2O.....................................................0.014g MgSO4·7H2O ..................................................0.002g pH 7.5 ± 0.2 at 25°C
bacterium tuberculosis.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix well and warm gently until dissolved. Distribute into test tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation and maintenance of Achromobacter species and Alcaligenes species.
Achromobacter Medium (ATCC Medium 589) Composition per liter: Agar ..................................................................20.0g K2HPO4 ...............................................................7.0g Methionine ..........................................................5.0g KH2PO4 ...............................................................2.0g (NH4)2SO4...........................................................1.0g Sodium citrate .....................................................0.4g MgSO4·7H2O ......................................................0.1g
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes.
Use: For the cultivation and maintenance of Achromobacter species.
Acid Egg Medium Composition per 1640.0mL:
Acid Tomato Broth Composition per liter: Glucose .............................................................10.0g Peptone .............................................................10.0g Yeast extract........................................................5.0g MgSO4·7H2O......................................................0.2g MnSO4·4H2O....................................................0.05g Tomato juice ............................................... 250.0mL L-Cysteine solution ......................................... 0.5mL L-Cysteine
Solution: Composition per 10.0mL: L-Cysteine ...........................................................0.1g
Preparation of L-Cysteine Solution: Add 0.1g of L-cysteine to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except L-cysteine solution, to distilled/deionized water and bring volume to 999.5mL. Mix thoroughly. Adjust pH to 4.8. Autoclave for 15 min at 15 psi pressure–121°C. Aseptically add 0.5mL of sterile Lcysteine solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation of a variety of fungi.
Actidione® Agar (Cycloheximide Agar) Composition per liter: Glucose .............................................................50.0g Agar ..................................................................15.0g Pancreatic digest of casein..................................5.0g Yeast extract........................................................4.0g KH2PO4.............................................................0.55g KCl..................................................................0.425g CaCl2·2H2O ....................................................0.125g MgSO4·7H2O ..................................................0.125g Bromocresol Green........................................22.0mg Actidione (cycloheximide) ............................10.0mg FeCl3 ................................................................2.5mg pH 5.5 ± 0.2 at 25°C
Potato starch......................................................30.0g KH2PO4 .............................................................12.3g Malachite Green..................................................0.4g MgSO4·7H2O ......................................................0.3g Penicillin G .............................................. 100,000IU Fresh egg mixture ..................................... 1000.0mL Glycerol ........................................................ 12.0mL
Source: Actidione Agar is available as a prepared medium from Oxoid Unipath.
Source: This medium is available as a prepared me-
Preparation of Medium: Add components to
dium from Oxoid Unipath.
Preparation of Medium: Add components to 1.0L of fresh egg mixture. Mix thoroughly. Gently heat and bring to boiling. Bring volume to 1640.0mL with distilled/deionized water. Distribute into tubes
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
16
Actinomyces Agar
Use: For the enumeration and detection of bacteria in specimens containing large numbers of yeasts and molds.
Actinomyces Agar Composition per liter: Agar ..................................................................20.0g K2HPO4 .............................................................13.0g Heart muscle, solids from infusion ...................10.0g Peptic digest of animal tissue............................10.0g Glucose ...............................................................5.0g Yeast extract........................................................5.0g NaCl ....................................................................5.0g Pancreatic digest of casein..................................4.0g KH2PO4 ...............................................................2.0g (NH4)2SO4...........................................................1.0g L-Cysteine·HCl·H2O............................................1.0g Soluble starch......................................................1.0g MgSO4·7H2O ......................................................0.2g CaCl2·2H2O.......................................................0.01g pH 6.9 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. If a semisolid medium is desired, add 7.0g of agar instead of 20.0g. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 10 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the maintenance or cultivation of a variety of anaerobic bacteria, including Actinomyces species, Eubacterium species, Fusobacterium species, Propionibacterium species, and others.
Actinomyces Broth Composition per liter: K2HPO4 .............................................................13.0g Heart muscle, solids from infusion ...................10.0g Peptic digest of animal tissue............................10.0g Glucose ...............................................................5.0g Yeast extract........................................................5.0g NaCl ....................................................................5.0g Pancreatic digest of casein..................................4.0g KH2PO4 ...............................................................2.0g (NH4)2SO4...........................................................1.0g L-Cysteine·HCl·H2O............................................1.0g Soluble starch......................................................1.0g MgSO4·7H2O ......................................................0.2g CaCl2·2H2O.......................................................0.01g pH 6.9 ± 0.2 at 25°C
Mix thoroughly. Distribute into tubes or flasks. Autoclave for 10 min at 15 psi pressure–121°C.
Use: For the maintenance or cultivation of a variety of anaerobic bacteria including Actinomyces species, Eubacterium species, Fusobacterium species, Propionibacterium species and others.
Actinomyces Broth Composition per liter: Beef heart, infusion from................................500.0g KH2PO4.............................................................15.0g Peptic digest of animal tissue ...........................10.0g Glucose ...............................................................5.0g Yeast extract........................................................5.0g NaCl....................................................................5.0g Pancreatic digest of casein..................................4.0g KH2PO4...............................................................2.0g (NH4)2SO4 ..........................................................1.0g L-Cysteine·HCl·H2O............................................1.0g Soluble starch......................................................1.0g MgSO4·7H2O ......................................................0.2g CaCl2·2H2O ......................................................0.02g pH 7.2 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 10 min at 15 psi pressure–121°C.
Use: For the maintenance or cultivation of a variety of anaerobic bacteria, including Actinomyces species, Eubacterium species, Fusobacterium species, Propionibacterium species, and others.
Actinomyces Isolation Agar Composition per liter: Agar ..................................................................15.0g Glycerol ..............................................................5.0g Sodium propionate..............................................4.0g Sodium caseinate ................................................2.0g K2HPO4...............................................................0.5g Asparagine ..........................................................0.1g MgSO4·7H2O ......................................................0.1g FeSO4·7H2O....................................................0.001g
Preparation of Medium: Add components to
powder from BD Diagnostic Systems.
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Preparation of Medium: Add components to
Use: For the isolation and cultivation of Actinomy-
distilled/deionized water and bring volume to 1.0L.
ces species.
Source: This medium is available as a premixed
AE Sporulation Medium, Modified
Actinomycete Growth Medium Composition per liter: Succinic acid .....................................................1.18g L-Glutamine.......................................................0.29g CaCl2·2H2O.........................................................0.2g KH2PO4 ...............................................................0.2g MgSO4·7H2O ......................................................0.2g NaCl ....................................................................0.1g m-Inositol ..........................................................0.09g Ferric EDTA....................................................0.037g MnSO4·H2O .....................................................4.5mg H3BO3 ..............................................................1.5mg ZnSO4·7H2O ....................................................1.5mg Nicotonic acid ..................................................0.5mg Pyridoxine-HCl................................................0.5mg Thiamine-HCl ..................................................0.1mg CuSO4·5H2O ..................................................0.04mg Na2MoO4·2H2O ...........................................0.025mg pH 6.4 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of actinomycetes.
Activated Carbon Medium (DSMZ Medium 811) Composition per liter: Agar ..................................................................15.0g Na2HPO4·12H2O.................................................9.0g Activated carbon .................................................5.0g KH2PO4 ...............................................................1.5g NH4Cl .................................................................1.5g MgSO4·7H2O ......................................................0.2g CaCl2·2H2O....................................................20.0mg NH4-Fe-III-Citrate ...........................................1.2mg Trace elements solution TS2........................... 1.0mL pH 7.5 ± 0.1 at 25°C
Trace Elements Solution TS2: Composition per liter: Na2MoO4·4H2O ...........................................900.0mg H3BO3 ..........................................................300.0mg CoCl2·6H2O .................................................200.0mg ZnSO4·7H2O ................................................100.0mg MnCl2·4H2O ..................................................30.0mg NiCl2·6H2O ....................................................20.0mg Na2SeO3 .........................................................20.0mg CuCl2·2H2O ...................................................10.0mg
Preparation of Solution A: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly.
Preparation of Medium: Add components, except activated carbon, to distilled/deionized water and
17
bring volume to 900.0mL. Mix thoroughly. After all components are dissolved add activated carbon. Bring volume to 1.0L with distilled/deionized water. Adjust pH to 7.5. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into Petri dishes or leave in tubes.
Use: For the cultivation of Streptomyces thermoautotrophicus.
AE Sporulation Medium, Modified Composition per 1079.2mL: Polypeptone™ ..................................................10.0g Yeast extract......................................................10.0g Na2HPO4 ..........................................................4.36g Ammonium acetate.............................................1.5g KH2PO4 ............................................................0.25g MgSO4·7H2O ......................................................0.2g Raffinose solution ......................................... 39.6mL Na2CO3 solution ........................................... 13.2mL CoCl2·6H2O solution .................................... 13.2mL Sodium ascorbate solution............................ 13.2mL pH 7.8 ± 0.1 at 25°C
Raffinose Solution: Composition per 100.0mL: Raffinose...........................................................10.0g
Preparation of Raffinose Solution: Add raffinose to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Na2CO3 Solution: Composition per 100.0mL: Na2CO3 ...............................................................7.0g
Preparation of Na2CO3 Solution: Add Na2CO3
to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
CoCl2 Solution: Composition per 100.0mL: CoCl2·6H2O......................................................0.32g
Preparation of CoCl2 Solution: Add CoCl2·6H2O to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Sodium Ascorbate Solution: Composition per 100.0mL: Sodium ascorbate................................................1.5g
Preparation of Sodium Ascorbate Solution: Add sodium ascorbate to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize. Use freshly prepared solution.
Preparation of Medium: Add components—except raffinose solution, Na2CO3 solution, CoCl2 solution, and sodium ascorbate solution—to distilled/ deionized water and bring volume to 1.0L. Mix thor-
18
Aeromonas Differential Agar
oughly. Adjust pH to 7.5 using 2m sodium carbonate solution. Distribute into tubes in 15.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C. Aseptically add 0.6mL of sterile raffinose solution, 0.2mL of sterile Na2CO3 solution, and 0.2mL of sterile CoCl2 solution to each tube. Mix thoroughly. Prior to inoculation, steam medium for 10 min. Cool to 25°C. Aseptically add 0.2mL of sterile sodium ascorbate solution to each tube.
Use: For the cultivation and sporulation of Clostridium perfringens.
Aeromonas Differential Agar (Dextrin Fuchsin Sulfite Agar) Composition per liter: Dextrin ..............................................................15.0g Agar ..................................................................13.0g Pancreatic digest of casein................................10.0g Na2HPO4 ...........................................................7.75g NaCl ....................................................................5.0g Beef extract .........................................................3.0g Na2SO3 ................................................................1.6g Acid Fuchsin solution ................................... 50.0mL pH 7.5 ± 0.2 at 25°C
Acid Fuchsin Solution: Composition per 50.0mL: Acid Fuchsin .....................................................0.25g Aquesou dioxan, 5% ..................................... 50.0mL
Preparation of Acid Fuchsin Solution: Add Acid Fuchsin to 50.0mL of 5% aqueous dioxan. Mix well to dissolve.
Caution: Acid Fuchsin is a potential carcinogen and care must be taken to avoid inhalation of the powdered dye and contamination of the skin.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the isolation and differentiation of Aeromonas species from other Gram-negative rods such as Pseudomonas and Enterobacteriaceae. Specimens with low numbers of Aeromonas may first be enriched by growth in starch broth for 4–9 days. After 24h of growth on this agar, colonies are sprayed with Nadi reagent (1% solution of N,N,N´,N´-tetramethylp-phenylene-diammonium dichloride). A positive Nadi reaction (dextrin degradation) is indicated by a purple color at the periphery of the colony. Dextrin fermentation is also indicated by red colonies. Aero-
monas species appear as large, convex, dark red colonies with a purple periphery.
Aeromonas hydrophila Medium Composition per liter: Inositol ..............................................................10.0g Pancreatic digest of casein................................10.0g L-Ornithine·HCl ..................................................5.0g Proteose peptone.................................................5.0g Agar ....................................................................3.0g Yeast extract........................................................3.0g Mannitol..............................................................1.0g Ferric ammonium citrate.....................................0.5g Na2S2O3·5H2O ....................................................0.4g Bromcresol Purple ............................................0.02g pH 6.7 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat until dissolved. Adjust pH to 6.7. Distribute into tubes in 5.0mL volumes. Autoclave for 12 min at 15 psi pressure–121°C.
Use: For the isolation and cultivation of Aeromonas hydrophila.
Aeromonas Medium (Ryan’s Aeromonas Medium) Composition per liter: Agar ..................................................................12.5g Na2S2O3 ..........................................................10.67g Proteose peptone.................................................5.0g NaCl....................................................................5.0g Xylose ...............................................................3.75g L-Lysine·HCl .......................................................3.5g Yeast extract........................................................3.0g Sorbitol ...............................................................3.0g Bile salts no. 3.....................................................3.0g Inositol ................................................................2.5g L-Arginine·HCl....................................................2.0g Lactose................................................................1.5g Ferric ammonium citrate.....................................0.8g Bromthymol Blue .............................................0.04g Thymol Blue .....................................................0.04g pH 8.0 ± 0.1 at 25°C
Source: This medium is available as a dehydrated powder from Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Do not autoclave. Cool to 50°C and aseptically add 5.0mg of ampicillin. Pour into sterile Petri dishes.
Use: For the isolation and selective differentiation of Aeromonas hydrophila and other Aeromonas species
AH5 Medium from clinical and nonclinical specimens. Aeromonas species appear as small (0.5–1.5mm), dark green colonies with darker centers.
AFPA (Aspergillus flavus/parasiticus Agar) Composition per liter: Yeast extract......................................................20.0g Agar ..................................................................15.0g Peptone..............................................................10.0g Ferric ammonium citrate.....................................0.5g Dichloran (Botran®)........................................2.0mg pH 6.3 ± 0.2 at 25°C
19
Preparation of Supplement Solution: Aseptically combine components. Mix thoroughly.
Fresh Yeast Extract Solution: Composition per 100.0mL: Baker’s yeast, live, pressed, starch-free............25.0g
Preparation of Fresh Yeast Extract Solution: Add the live Baker’s yeast to 100.0mL of distilled/ deionized water. Autoclave for 90 min at 15 psi pressure–121°C. Allow to stand. Remove supernatant solution. Adjust pH to 6.6–6.8. Penicillin Solution: Composition per 10.0mL:
Source: This medium is available as a dehydrated
Penicillin G ............................................. 1,000,000U
powder from Oxoid Unipath.
Preparation of Penicillin Solution: Add peni-
Preparation of Medium: Add components to
cillin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Add 100.0mg of chloramphenicol. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes.
Use: For the selective isolation and enumeration of Aspergillus flavus and Aspergillus parasiticus. Colonies of these fungi appear with dark yellow-orange color on the reverse side.
AH5 Medium Composition per 205.9mL: Agar base .................................................... 160.0mL Supplement solution ..................................... 45.9mL pH 6.0 ± 0.2 at 25°C
Agar Base: Composition per 165.0mL: Pancreatic digest of casein................................2.72g Agar ....................................................................2.1g NaCl ....................................................................0.8g Papaic digest of soybean meal ..........................0.48g K2HPO4 ...............................................................0.4g Glucose ...............................................................0.4g
Preparation of Agar Base: Add components, ex-
CVA Enrichment: Composition per liter: Glucose ...........................................................100.0g L-Cysteine·HCl·H2O..........................................25.9g L-Glutamine ......................................................10.0g L-Cystine·2HCl ...................................................1.0g Adenine...............................................................1.0g Nicotinamide adenine dinucleotide ..................0.25g Cocarboxylase.....................................................0.1g Guanine·HCl .....................................................0.03g Fe(NO3)3 ...........................................................0.02g p-Aminobenzoic acid......................................0.013g Vitamin B12 .......................................................0.01g Thiamine·HCl ..................................................3.0mg
Preparation of CVA Enrichment: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize. L-Cysteine·HCl·H2O
Solution: Composition per 10.0mL: L-Cysteine·HCl·H2O............................................0.4g
Preparation of L-Cysteine·HCl·H2O Solution: Add L-cysteine·HCl·H2O solution to distilled/
cept agar, to distilled/deionized water and bring volume to 165.0mL. Adjust pH to 5.5. Add agar. Mix thoroughly. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C.
deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Supplement Solution: Composition per 45.9mL:
Urea.....................................................................1.0g
Horse serum, unheated.................................. 40.0mL Fresh yeast extract solution............................. 2.0mL Penicillin solution ........................................... 2.0mL CVA enrichment.............................................. 1.0mL L-Cysteine·HCl·H2O solution ......................... 0.5mL Urea solution................................................... 0.4mL
Urea Solution: Composition per 10.0mL: Preparation of Urea Solution: Add urea to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Aseptically combine cooled, sterile components. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
20
AKI Medium
Use: For the cultivation of Ureaplasma urealyticum from urine and exudates and for the cultivation of other Ureaplasma species.
AKI Medium Composition per liter: Peptone..............................................................15.0g NaCl ....................................................................5.0g Yeast extract........................................................4.0g Sodium bicarbonate solution ........................ 30.0mL pH 7.2 ± 0.2 at 25°C
Sodium Bicarbonate Solution: Composition per 100.0mL: NaHCO3 ............................................................10.0g
Preparation of Sodium Bicarbonate Solution: Add sodium bicarbonate to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize. Use freshly prepared solution.
NH4Cl ...............................................................1.07g Na2SO4 ..............................................................0.43g Na2HPO4·12H2O...............................................0.23g MgCl2·6H2O .......................................................0.2g CaCl2·2H2O ......................................................0.03g Ferric ammonium citrate.................................0.005g Sodium succinate solution ............................ 10.0mL CuSO4 solution ............................................... 2.5mL Trace elements solution SL-7 ......................... 1.0mL
Sodium Succinate Solution: Composition per 100.0mL: Sodium succinate ..............................................40.0g
Preparation of Sodium Succinate Solution: Add sodium succinate to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
CuSO4 Solution: Composition per 100.0mL:
Preparation of Medium: Add components, except
CuSO4 ...............................................................16.0g
sodium bicarbonate solution, to distilled/deionized water and bring volume to 970.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile sodium bicarbonate solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks. Prepare medium freshly.
Preparation of CuSO4 Solution: Add CuSO4 to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Use: For the cultivation of Vibrio cholerae and other Vibrio species.
Alcaligenes Agar Composition per liter: Agar ..................................................................10.0g Peptone................................................................5.0g Ammonium lactate..............................................3.0g Meat extract ........................................................3.0g Ferric citrate........................................................0.2g pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Add ferric citrate to distilled/deionized water and bring volume to 100.0mL. In a separate flask, add remaining components to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Adjust pH to 7.0. Steam the two solutions for 20 min on three consecutive days. Aseptically combine the two solutions. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation of Alcaligenes species.
Alcaligenes Medium Composition per liter: Tris ....................................................................6.06g NaCl ..................................................................4.68g KCl....................................................................1.49g
Trace Elements Solution SL-7: Composition per 1001.0mL: CoCl2·6H2O .................................................200.0mg MnCl2·4H2O ................................................100.0mg ZnCl2 ..............................................................70.0mg H3BO3 ............................................................60.0mg Na2MoO4·2H2O .............................................40.0mg CuCl2·2H2O ...................................................20.0mg NiCl2·6H2O ....................................................20.0mg HCl (25%)....................................................... 1.0mL
Preparation of Trace Elements Solution SL-7: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly.
Preparation of Medium: Add components, except CuSO4 solution and sodium succinate solution, to distilled/deionized water and bring volume to 987.5mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Aseptically add 10.0mL of sterile CuSO4 solution and 2.5mL of sterile sodium succinate solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation of Alcaligenes species.
Alcaligenes N5 Medium Composition per liter: Sodium succinate·2H2O......................................5.0g KH2PO4.............................................................0.75g NH4Cl ...............................................................0.67g K2HPO4.............................................................0.61g MgSO4·7H2O ......................................................0.2g
Alginate Utilization Medium CaCl2· 2H2O......................................................0.03g MnCl2·4H2O ....................................................3.0mg FeCl3 ................................................................2.4mg Na2MoO4·2H2O ...............................................1.0mg
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation and maintenance of Alcaligenes faecalis.
Alcaligenes NA YE Medium (Alcaligenes Nutrient Agar Yeast Extract Medium) Composition per liter: Agar ..................................................................15.0g Pancreatic digest of gelatin .................................5.0g Yeast extract........................................................5.0g Beef extract .........................................................3.0g pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of Alcaligenes species.
Alcaligenes NB YE Agar (Alcaligenes Nutrient Broth Yeast Extract Agar)
21
Yeast extract........................................................5.0g Beef extract.........................................................3.0g
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of Alcaligenes faecalis.
Alcaligenes NB YE Medium (Alcaligenes Nutrient Broth Yeast Extract Medium) Composition per liter: Pancreatic digest of gelatin.................................5.0g Yeast extract........................................................5.0g Beef extract.........................................................3.0g pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation and maintenance of Alcaligenes species.
Alginate Utilization Medium Composition per liter: Solution B ................................................... 500.0mL Solution A................................................... 400.0mL Solution C ................................................... 100.0mL
Solution A: Composition per 400.0mL:
Composition per liter:
Marine salts.......................................................38.0g
Agar ..................................................................15.0g Pancreatic digest of gelatin .................................5.0g Yeast extract........................................................5.0g Beef extract .........................................................3.0g
Preparation of Solution A: Add marine salts to
Preparation of Medium: Add components to
Solution B: Composition per 500.0mL:
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of Alcaligenes faecalis.
Alcaligenes NB YE Broth (Alcaligenes Nutrient Broth Yeast Extract Broth) Composition per liter: Pancreatic digest of gelatin .................................5.0g
distilled/deionized water and bring volume to 400.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C.
Agar ..................................................................20.0g Sodium alginate ................................................10.0g
Preparation of Solution B: Add components to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Solution C: Composition per 100.0mL: Tris·HCl buffer................................................0.067g NaNO3 ............................................................0.047g Ferric EDTA ..................................................66.5mg Sodium glycerophosphate..............................6.67mg
22
Alkaline Peptone Agar
Thiamine·HCl ................................................ 67.0µg Vitamin B12 ...................................................... 1.3µg Biotin ............................................................. 0.67µg
tubes or flasks. Autoclave for 10 min at 15 psi pressure–121°C.
Preparation of Solution C: Add components to
erae and other Vibrio species.
distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Use: For the cultivation and transport of Vibrio chol-
Alkaline Peptone Water
Preparation of Medium: Aseptically combine
Composition per liter:
solutions A, B, and C. For liquid medium, omit agar from solution B.
Peptone .............................................................10.0g NaCl....................................................................5.0g pH 9.0 ± 0.2 at 25°C
Use: For the cultivation of microorganisms that can utilize alginate as a carbon source. Growth on alginate (production of alginase) is a diagnostic test used in the differentiation of Vibrio species.
Alkaline Peptone Agar Composition per liter: NaCl ..................................................................20.0g Agar ..................................................................15.0g Peptone..............................................................10.0g pH 8.5 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 9.0. Distribute into tubes or flasks. Autoclave for 20 min at 15 psi pressure–121°C.
Use: For the cultivation of a variety of alkalophilic microorganisms, especially Vibrio species.
Alkvisco Medium Composition per liter:
Use: For the cultivation of Vibrio cholerae and other
Agar ..................................................................15.0g Beef extract.......................................................10.0g Peptone .............................................................10.0g NaCl....................................................................5.0g Acrylonitrile........................................................0.5g KCN...............................................................10.0mg pH 6.5-8.0 at 25°C
Vibrio species.
Caution: Cyanide is toxic. Acrylonitrile is a carcin-
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Adjust pH to 8.5. Distribute into tubes. Autoclave for 15 min at 15 psi pressure–121°C. Allow tubes to cool in a slanted position.
ogen; use appropriate precautions.
Alkaline Peptone Salt Broth (APS Broth) Composition per liter: NaCl ..................................................................30.0g Peptone..............................................................10.0g
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 8.5. Distribute into tubes in 10.0mL volumes. Autoclave for 10 min at 15 psi pressure–121°C.
Use: For the cultivation of Vibrio cholerae and other Vibrio species.
Alkaline Peptone Water Composition per liter: NaCl ..................................................................10.0g Peptone..............................................................10.0g pH 8.5 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 8.5. Distribute into
Preparation of Medium: Add components, except acrylonitrile, to distilled/deionized water and bring volume to 980.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 10 min at 15 psi pressure–121°C. Add acrylonitrile to 20.0mL of distilled/deionized water and filter sterilize. Add aseptically to the sterile basal medium.
Use: For the cultivation and maintenance of Corynebacterium species.
Allantoin Agar Composition per liter: Agar ..................................................................15.0g Na2HPO4·12H2O ................................................9.0g NaCl....................................................................5.0g KH2PO4 ..............................................................1.5g Meat extract ........................................................1.0g Yeast extract........................................................1.0g MgSO4·7H2O......................................................0.2g MnCl2·4H2O ..................................................20.0mg CaCl2 ...............................................................1.2mg Glucose-allantoin solution .......................... 100.0mL
ALOA Medium Glucose-Allantoin Solution: Composition per 100.0mL: Glucose ...............................................................5.0g Allantoin .............................................................1.0g
Preparation of Glucose-Allantoin Solution: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize. Warm to 50°C.
Preparation of Medium: Add components, except glucose-allantoin solution, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Aseptically add 100.0mL of sterile glucose-allantoin solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation and maintenance of Bacillus species.
Allantoin Broth Composition per liter: Na2HPO4·12H2O ................................................9.0g NaCl ....................................................................5.0g KH2PO4 ..............................................................1.5g Meat extract ........................................................1.0g Yeast extract........................................................1.0g MgSO4·7H2O......................................................0.2g MnCl2·4H2O ..................................................20.0mg CaCl2................................................................1.2mg Glucose-allantoin solution .......................... 100.0mL
Glucose-Allantoin Solution: Composition per 100.0mL: Glucose ...............................................................5.0g Allantoin .............................................................1.0g
Preparation of Glucose-Allantoin Solution: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, ex-
23
Peptone .............................................................18.0g LiCl ...................................................................10.0g Yeast extract......................................................10.0g Tryptone..............................................................6.0g NaCl....................................................................5.0g Na2HPO4 .............................................................2.5g Na-pyruvate ........................................................2.0g Glucose ...............................................................2.0g Mg-glycerophosphate .........................................1.0g MgSO4 ................................................................0.5g 5-Bromo4-chloro-indolylβ-D-glucopyranoside ..................................0.05g Phosphatidylinositol solution........................ 50.0mL Nalidixic acid solution.................................... 5.0mL Ceftazidime solution....................................... 5.0mL Cycloheximide solution .................................. 5.0mL Polymyxin B solution ..................................... 5.0mL pH 7.2 ± 0.2 at 25°C
Nalidixic Acid Solution: Composition per 5.0mL: Nalidixic acid....................................................0.02g
Preparation of Nalidixic Acid Solution: Add nalidixic acid to distilled/deionized water and bring volume to 5.0mL. Mix thoroughly. Filter sterilize. Ceftazidime Solution: Composition per 5.0mL: Ceftazidime.........................................................1.5g
Preparation of Ceftazidime Solution: Add ceftazidime to distilled/deionized water and bring volume to 5.0mL. Mix thoroughly. Filter sterilize. Cycloheximide Solution: Composition per 5.0mL: Cycloheximide..................................................0.05g Ethanol............................................................ 2.5mL
Preparation of Cycloheximide Solution: Add cycloheximide to 2.5mL of ethanol. Mix thoroughly. Bring volume to 5.0mL with distilled/deionized water. Filter sterilize. Polymyxin B Solution: Composition per 5.0mL:
cept glucose-allantoin solution, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Aseptically add 100.0mL of sterile glucose-allantoin solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Preparation of Lioncomycin Solution: Add polymyxin B to distilled/deionized water and bring volume to 5.0mL. Mix thoroughly. Filter sterilize.
Use: For the cultivation and maintenance of Bacillus species.
Phosphatidylinositol Solution: Composition per 5.0mL:
Polymyxin B ................................................. 76700U
Polymyxin B ................................................. 76700U
ALOA Medium (Agar Listeria Ottavani & Agosti) Composition per liter: Agar ..................................................................18.0g
Preparation of Phosphatidylinositol Solution: Add phosphatidylinositol to cold distilled/ deionized water and bring volume to 50.0mL. Stir for 30 min so a homogeneous suspension is obtained.
24
ALP Basal Medium
Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C.
Preparation of Medium: Add components, ex-
ALP Basal Medium (Aerobic Low Peptone Basal Medium) Composition per liter:
cept phosphatidylinositol solution, nalidixic acid solution, cetazidime solution, cycloheximide solution, and polymyxin B solution, to distilled/deionized water and bring volume to 930.0mL. Mix thoroughly. Adjust the pH to 7.2. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 50.0mL sterile phosphatidylinositol solution, 5.0mL sterile nalidixic acid solution, 5.0mL sterile cetazidime solution, 5.0mL sterile cycloheximide solution, and 5.0mL sterile polymyxin B solution. Mix thoroughly. Pour into the Petri dishes or distribute into sterile tubes.
Agar ..................................................................15.0g (NH4)2SO4 ..........................................................1.0g Pancreatic digest of casein..................................0.5g Yeast extract........................................................0.5g Glucose ...............................................................0.2g MgSO4·7H2O ......................................................0.2g KCl......................................................................0.2g Phenol Red........................................................0.02g Substrate solution.......................................... 50.0mL pH 6.5 ± 0.2 at 25°C
Use: For the isolaltion and cultivation of Literia spp.
Substrate .............................................................0.1g
Substrate Solution: Composition per 50.0mL: Preparation of Substrate Solution: Add sub-
ALP Basal Medium (Aerobic Low Peptone Basal Medium) Composition per liter: Agar ..................................................................15.0g (NH4)2SO4...........................................................1.0g Pancreatic digest of casein..................................0.5g Yeast extract........................................................0.5g MgSO4·7H2O ......................................................0.2g KCl......................................................................0.2g Phenol Red........................................................0.02g Substrate solution.......................................... 50.0mL pH 7.8 ± 0.2 at 25°C
Substrate Solution: Composition per 50.0mL: Substrate..............................................................0.1g
Preparation of Substrate Solution: Add substrate to distilled/deionized water and bring volume to 50.0mL. Use sugars, carbohydrates, n-butanol, other alcohols, or any acidogenic carbon source. Mix thoroughly. Filter sterilize.
strate to distilled/deionized water and bring volume to 50.0mL. Use gelatin, aliphatic acids, or any alkalogenic carbon source. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except substrate solution, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Adjust pH to 6.5. Distribute into screw-capped tubes in 3.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 0.15mL of sterile substrate solution to each tube. Mix thoroughly. Allow tubes to cool in a slanted position.
Use: For the cultivation and differentiation of microorganisms based on their ability to utilize a variety of carbon sources such as gelatin, aliphatic acids, and other alkalophilic substrates.
Amies Modified Transport Medium with Charcoal Composition per liter:
cept substrate solution, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Adjust pH to 7.8. Distribute into screw-capped tubes in 3.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 0.15mL of sterile substrate solution to each tube. Mix thoroughly. Allow tubes to cool in a slanted position.
Charcoal............................................................10.0g Agar ....................................................................4.0g NaCl....................................................................3.0g Na2HPO4 ...........................................................1.15g Sodium thioglycolate ..........................................1.0g KCl......................................................................0.2g KH2PO4...............................................................0.2g CaCl2·2H2O ........................................................0.1g MgCl2·6H2O .......................................................0.1g pH 7.2 ± 0.2 at 25°C
Use: For the cultivation and differentiation of micro-
Source: This medium is available as a premixed
organisms based on their ability to utilize a variety of carbon sources such as carbohydrates, alcohols, and other acidogenic substrates.
Preparation of Medium: Add components to
Preparation of Medium: Add components, ex-
powder from BD Diagnostic Systems. distilled/deionized water and bring volume to 1.0L.
AMO.1 Medium Mix thoroughly. Gently heat and bring to boiling. Distribute into flasks or tubes. Autoclave for 20 min at 15 psi pressure–121°C. While cooling, turn tubes to uniformly suspend charcoal.
Use: For the transport of swab specimens to prolong the survival of microorganisms, especially Neisseria gonorrhoeae, between collection and culturing. Addition of charcoal to this medium neutralizes metabolic products that may be toxic to Neisseria gonorrhoeae.
Amies Modified Transport Medium with Charcoal Composition per liter: Charcoal ............................................................10.0g NaCl ....................................................................8.0g Agar ....................................................................3.6g Na2HPO4 ...........................................................1.15g Sodium thioglycolate ..........................................1.0g KCl......................................................................0.2g KH2PO4 ...............................................................0.2g CaCl2·2H2O.........................................................0.1g MgCl2·6H2O .......................................................0.1g pH 7.2 ± 0.2 at 25°C
25
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into flasks or tubes. Autoclave for 20 min at 15 psi pressure–121°C.
Use: For the transport of swab specimens to prolong the survival of microorganisms, especially Neisseria gonorrhoeae, between collection and culturing.
Amies Transport Medium without Charcoal Composition per liter: NaCl....................................................................8.0g Agar ....................................................................3.6g Na2HPO4 ...........................................................1.15g Sodium thioglycolate ..........................................1.0g KCl......................................................................0.2g KH2PO4...............................................................0.2g CaCl2·2H2O ........................................................0.1g MgCl2·6H2O .......................................................0.1g pH 7.2 ± 0.2 at 25°C
Source: This medium is available as a premixed
Source: This medium is available as a premixed
powder from BD Diagnostic Systems and Oxoid Unipath.
powder from BD Diagnostic Systems.
Preparation of Medium: Add components to
Preparation of Medium: Add components to
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into flasks or tubes. Autoclave for 20 min at 15 psi pressure–121°C.
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into flasks or tubes. Autoclave for 20 min at 15 psi pressure–121°C. While cooling, turn tubes to uniformly suspend charcoal.
Use: For the transport of swab specimens to prolong the survival of microorganisms, especially Neisseria gonorrhoeae, between collection and culturing. Addition of charcoal to this medium neutralizes metabolic products that may be toxic to Neisseria gonorrhoeae.
Amies Transport Medium without Charcoal Composition per liter: Agar ....................................................................4.0g NaCl ....................................................................3.0g Na2HPO4 ...........................................................1.15g Sodium thioglycolate ..........................................1.0g KCl......................................................................0.2g KH2PO4 ...............................................................0.2g CaCl2·2H2O.........................................................0.1g MgCl2·6H2O .......................................................0.1g pH 7.2 ± 0.2 at 25°C
Use: For the transport of swab specimens to prolong the survival of microorganisms, especially Neisseria gonorrhoeae, between collection and culturing.
AMO.1 Medium Composition per 1012.0mL: Yeast extract......................................................10.0g NaCl....................................................................5.8g N-Methylhydantoin...........................................5.64g NaHCO3 ..............................................................4.5g L-Serine...............................................................2.0g L-Threonine.........................................................2.0g Pancreatic digest of casein..................................0.5g L-Cysteine ...........................................................0.5g MgCl2·6H2O .......................................................0.4g KCl......................................................................0.3g NH4Cl ...............................................................0.27g KH2PO4...............................................................0.2g CaCl2·2H2O ......................................................0.15g Wolfe’s vitamin solution............................... 10.0mL
26
Ampicillin Kanamycin Nutrient Agar
Na2HSeO3 solution.......................................... 1.0mL Trace elements solution SL-10 ....................... 1.0mL pH 8.3 ± 0.2 at 25°C
Wolfe’s Vitamin Solution: Composition per liter: Pyridoxine·HCl ..............................................10.0mg p-Aminobenzoic acid.......................................5.0mg Lipoic acid .......................................................5.0mg Nicotinic acid ...................................................5.0mg Riboflavin ........................................................5.0mg Thiamine·HCl ..................................................5.0mg Calcium DL-pantothenate.................................5.0mg Biotin ...............................................................2.0mg Folic acid..........................................................2.0mg Vitamin B12 ......................................................0.1mg
Preparation of Wolfe’s Vitamin Solution:
tically and anaerobically distribute into sterile tubes or bottles.
Use: For the cultivation of Tissierella creatinini.
Ampicillin Kanamycin Nutrient Agar Composition per liter: Agar ..................................................................15.0g Peptone ...............................................................5.0g NaCl....................................................................5.0g Yeast extract........................................................2.0g Beef extract.........................................................1.0g Ampicillin solution ....................................... 10.0mL Kanamycin solution ...................................... 10.0mL
Ampicillin Solution: Composition per 10.0mL:
Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly.
Ampicillin ......................................................50.0mg
Na2SeO3 Solution: Composition per liter:
ampicillin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Na2SeO3·5H2O.................................................0.2mg
Kanamycin Solution: Composition per 10.0mL:
Preparation of Na2SeO3 Solution: Add
Na2SeO3·5H2O to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Sparge with 100% N2. Autoclave for 15 min at 15 psi pressure– 121°C.
Trace Elements Solution SL-10: Composition per liter: FeCl2·4H2O .........................................................1.5g CoCl2·6H2O .................................................190.0mg MnCl2·4H2O ................................................100.0mg ZnCl2 ..............................................................70.0mg Na2MoO4·2H2O .............................................36.0mg NiCl2·6H2O ....................................................24.0mg H3BO3 ..............................................................6.0mg CuCl2·2H2O .....................................................2.0mg HCl (25% solution)....................................... 10.0mL
Preparation of Trace Elements Solution SL-10: Add FeCl2·4H2O to 10.0mL of HCl solution. Mix thoroughly. Add distilled/deionized water and bring volume to 1.0L. Add remaining components. Mix thoroughly. Sparge with 100% N2. Autoclave for 15 min at 15 psi pressure–121°C.
Preparation of Medium: Prepare anaerobically. Add components, except NaHCO3 and L-cysteine, to distilled/deionized water and bring volume to 1.0L. Sparge with 100% N2 for 30 min. Adjust pH to 8.3 with 10N NaOH. Add NaHCO3 and L-cysteine (solid substances). Mix thoroughly. Sparge with 80% N2 + 20% CO2 mixture. Flush the headspace of the medium vessel with the 80% N2 + 20% CO2 mixture. Autoclave for 15 min at 15 psi pressure–121°C. Sparge with 80% N2 + 20% CO2 mixture for 30 min. Asep-
Preparation of Ampicillin Solution: Add
Kanamycin.....................................................25.0mg
Preparation of Kanamycin Solution: Add kanamycin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except ampicllin solution and kanmycin solution, to distilled/deionized water and bring volume to 980.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Aseptically add 10.0mL of sterile ampicillin solution and 10.0mL of sterile kanamycin solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation of fungi and various antibiotic-resitant bacteria, including Escherichia coli.
Ampicillin L Broth Medium Composition per liter: Pancreatic digest of casein................................10.0g NaCl....................................................................5.0g Yeast extract........................................................5.0g Glucose ...............................................................1.0g Ampicillin solution ....................................... 10.0mL pH 7.0 ± 0.2 at 25°C
Ampicillin Solution: Composition per 10.0mL: Ampicillin ......................................................50.0mg
Preparation of Ampicillin Solution: Add ampicillin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Anaerobe Agar Preparation of Medium: Add components, except ampicillin solution, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Bring pH to 7.0. Autoclave for 15 min at 15 psi pressure–121°C. Aseptically add 10.0mL of sterile ampicillin solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation of Escherichia coli.
Ampicillin TY Salt Medium
27
clave for 20 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile amygdalin solution. Mix thoroughly. Aseptically distribute into sterile tubes with cotton plugs. Allow tubes to cool in a slanted position, forming a short slant.
Use: For the cultivation and differentiation of Serratia species based on their ability to produce acid and HCN from amygdalin.
Anaerobe Agar
Composition per liter:
Composition per 1001.5mL:
NaCl ..................................................................10.0g Pancreatic digest of casein................................10.0g Yeast extract........................................................5.0g Ampicillin solution ....................................... 10.0mL pH 7.0 ± 0.2 at 25°C
Agar ..................................................................15.0g Pancreatic digest of casein................................15.0g Pancreatic digest of soybean meal......................5.0g NaCl....................................................................5.0g L-Cysteine·HCl·H2O solution.......................... 5.0mL Vitamin K1 solution ..................................... 1.0mL Hemin solution................................................ 0.5mL pH 7.0 ± 0.2 at 25°C
Ampicillin Solution: Composition per 10.0mL: Ampicillin ......................................................50.0mg
Preparation of Ampicillin Solution: Add ampicillin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except ampicillin solution, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Bring pH to 7.0. Autoclave for 15 min at 15 psi pressure–121°C. Aseptically add 10.0mL of sterile ampicillin solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation of various antibiotic resistant bacteria, including Escherichia coli.
Amygdalin Medium Composition per liter: Peptone..............................................................10.0g Beef extract .........................................................5.0g NaCl ....................................................................5.0g Agar ....................................................................3.0g Amygdalin solution..................................... 200.0mL Bromthymol Blue (0.05% solution)................ 5.0mL pH 7.0 ± 0.2 at 25°C
Amygdalin Solution: Composition per 200.0mL: Amygdalin ........................................................10.0g
Preparation of Amygdalin Solution: Add amygdalin to distilled/deionized water and bring volume to 200.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except amygdalin solution, to distilled/deionized water and bring volume to 800.0mL. Mix thoroughly. Gently heat and bring to boiling. Adjust pH to 7.0. Auto-
L-Cysteine·HCl·H2O
Solution: Composition per 5.0mL: L-Cysteine·HCl·H2O............................................0.4g
NaOH (1N solution)........................................ 5.0mL
Preparation of L-Cysteine·HCl·H2O Solution: Add L-cysteine·HCl·H2O to 5.0mL 1N NaOH. Mix thoroughly. Filter sterilize.
Hemin Solution: Composition per 100.0mL: Hemin .................................................................1.0g
Preparation of Hemin Solution: Add hemin to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool. Refrigerate at 4°C for storage.
Vitamin K1 Solution: Composition per 100.0mL: Vitamin K1 ..........................................................1.0g Ethanol, absolute........................................... 20.0mL
Preparation of Vitamin K1 Solution: Add vita-
min K1 to 100.0mL of 95% ethanol. Mix thoroughly. Solution may require 2–3 days with intermittent shaking to completely dissolve. Filter sterilize. Refrigerate at 4°C for storage.
Preparation of Medium: Add components, exhemin solution and vitamin K1 solution, to distilled/ deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Adjust pH to 7.0 ± 0.2 at 25°C. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 0.5mL of sterile hemin solution and 1.0mL of sterile vitamin K1 solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes. Reduce
28
Anaerobe Agar
medium for 24h by incubation in an anaerobic glove box of GasPak jar prior to use.
Use: For the cultivation of anaerobic bacteria such as Brucella and Clostridium spp.
Anaerobe Agar (LMG Medium 41) Composition per liter: Agar Base.................................................... 800.0mL Solution A ................................................... 100.0mL Solution B ................................................... 100.0mL pH 6.9 ± 0.2 at 25°C
Agar Base: Composition per 800.0mL: Agar ................................................................. 30.5g Tryptone ..............................................................5.0g Yeast extract........................................................5.0g (NH4)2SO4...........................................................0.5g Sodium thioglycolate ..........................................0.5g MgSO4·7H2O ......................................................0.1g Fe(NH4)2(SO4)2·6H2O ...................................55.0mg Na2MoO4·2H2O ...............................................2.4mg Na2SeO3·5H2O...............................................0.23mg
Preparation of Agar Base: Add components to distilled/deionized water and bring volume to 800.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C.
Solution A: Composition per 100.0mL: Glucose .............................................................18.0g K2HPO4 ...............................................................7.0g KH2PO4 ...............................................................5.5g
Preparation of Solution A: Add components to 100.0mL of distilled/deionized water. Mix thoroughly. Filter sterilize. Solution B: Composition per 100.0mL: NaHCO3 ............................................................10.0g
Anaerobe Medium (LMG Medium 41) Composition per liter: Agar Base.................................................... 800.0mL Solution A................................................... 100.0mL Solution B ................................................... 100.0mL pH 6.9 ± 0.2 at 25°C
Agar Base: Composition per 800.0mL: Tryptone..............................................................5.0g Yeast extract........................................................5.0g (NH4)2SO4 ..........................................................0.5g Sodium thioglycolate ..........................................0.5g Agar ................................................................... 0.5g MgSO4·7H2O ......................................................0.1g Fe(NH4)2(SO4)2·6H2O ...................................55.0mg Na2MoO4·2H2O ...............................................2.4mg Na2SeO3·5H2O...............................................0.23mg
Preparation of Agar Base: Add components to distilled/deionized water and bring volume to 800.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C.
Solution A: Composition 100.0mL: Glucose .............................................................18.0g K2HPO4...............................................................7.0g KH2PO4...............................................................5.5g
Preparation of Solution A: Add components to 100.0mL of distilled/deionized water. Mix thoroughly. Filter sterilize. Solution B: Composition 100.0mL: NaHCO3 ............................................................10.0g
Preparation of Solution B: Add components to 100.0mL of distilled/deionized water. Mix thoroughly. Filter sterilize.
Preparation of Medium: Aseptically add solutions A and B to the sterile Agar Base. Adjust pH to 6.9. Mix thoroughly. Distribute into sterile tubes. Incubate anaerobically under 100% CO2 gas atmosphere.
Preparation of Solution B: Add NaHCO3 to 100.0mL of distilled/deionized water. Mix thoroughly. Filter sterilize.
Use: For the cultivation of anerobic bacteria.
Preparation of Medium: Aseptically add solu-
Composition per liter:
tions A and B to the agar base. Adjust pH to 6.9. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes. Incubate anaerobically under 100% CO2 gas atmosphere.
Use: For the cultivation of anerobic bacteria.
Anaerobic Agar Agar ..................................................................20.0g Pancreatic digest of casein................................20.0g Glucose .............................................................10.0g NaCl....................................................................5.0g Sodium thioglycolate ..........................................2.0g
Anaerobic Egg Yolk Agar
29
Sodium formaldehyde sulfoxylate ......................1.0g Methylene Blue................................................2.0mg pH 7.2 ± 0.2 at 25°C
Use: For the cultivation of a variety of anaerobic and
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Anaerobic CNA Agar (Anaerobic Colistin Nalidixic Acid Agar)
Preparation of Medium: Add components to dis-
Composition per liter:
tilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Adjust pH to 7.2. Distribute into tubes until medium is 3 inches deep. Autoclave for 15 min at 15 psi pressure–121°C.
Agar ..................................................................13.0g Pancreatic digest of casein................................12.0g Peptic digest of animal tissue .............................5.0g NaCl....................................................................5.0g Yeast extract........................................................3.0g Beef extract.........................................................3.0g Cornstarch...........................................................1.0g Glucose ...............................................................1.0g L-Cysteine·HCl·H2O............................................0.5g Vitamin K1 .....................................................10.0mg Hemin ............................................................10.0mg Colistin...........................................................10.0mg Nalidixic acid.................................................10.0mg Sheep blood, defibrinated ............................. 50.0mL
Use: For the cultivation of a variety of anaerobic microorganisms, especially Clostridium species.
Anaerobic Agar Composition per liter: Pancreatic digest of casein................................17.5g Agar ..................................................................15.0g Glucose .............................................................10.0g Papaic digest of soybean meal ............................2.5g NaCl ....................................................................2.5g Sodium thioglycolate ..........................................2.0g Sodium formaldehyde sulfoxylate ......................1.0g L-Cystine .............................................................0.4g Methylene Blue................................................2.0mg pH 7.2 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Use with Brewer anaerobic Petri dishes or in tubes or ordinary plates and incubate in anaerobic jars.
Use: For the cultivation of Clostridium species and for anaerobic microorganisms.
Anaerobic Broth Composition per liter: Pancreatic digest of casein................................17.5g Glucose .............................................................10.0g NaCl ....................................................................2.5g Papaic digest of soybean meal ............................2.5g Sodium thioglycolate ..........................................2.0g Sodium formaldehyde sulfoxylate ......................1.0g L-Cystine .............................................................0.4g Methylene Blue................................................2.0mg pH 7.2 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
microaerophilic microorganisms.
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components, except sheep blood, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 50.0mL of sterile, defibrinated sheep blood. Mix thoroughly. Pour into sterile Petri dishes.
Use: For the selective isolation of anaerobic streptococci.
Anaerobic Egg Yolk Agar Composition per 1080.0mL: Agar ..................................................................20.0g Proteose peptone...............................................20.0g NaCl....................................................................5.0g Pancreatic digest of casein..................................5.0g Yeast extract........................................................5.0g Egg yolk emulsion, 50%............................... 80.0mL pH 7.0 ± 0.2 at 25°C
Egg Yolk Emulsion, 50%: Composition per 100.0mL: Chicken egg yolks.................................................. 11 Whole chicken egg ..................................................1 NaCl (0.9% solution) .................................... 50.0mL
Preparation of Egg Yolk Emulsion, 50%: Soak whole eggs with 1:100 dilution of saturated mercuric chloride solution for 1 min. Crack eggs and separate yolks from whites. Mix egg yolks with 1 chicken egg. Beat to form emultion. Measure 50.0mL of egg yolk emulsion and add to 50.0mL of
30
Anaerobic Egg Yolk Agar
0.9% NaCl solution. Mix thoroughly. Filter sterilize. Warm to 45°–50°C.
Preparation of Medium: Add components, except egg yolk emulsion, 50%, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 80.0mL of sterile egg yolk emulsion, 50%. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes. Allow plates to dry at 35°C for 24h.
Use: For the cultivation of Clostridium species.
Anaerobic Egg Yolk Agar
Yeast extract........................................................5.0g Egg yolk emulsion, 50%............................... 20.0mL pH 7.0 ± 0.2 at 25°C
Egg Yolk Emulsion, 50%: Composition per 100.0mL: Chicken egg yolks....................................................2 NaCl (0.9% solution) .................................... 10.0mL
Preparation of Egg Yolk Emulsion, 50%: Soak eggs with 1:100 dilution of saturated mercuric chloride solution for 1 min. Crack eggs and separate yolks from whites. Beat to form emultion. Measure 10.0mL of egg yolk emulsion and add to 10.0mL of 0.9% NaCl solution. Mix thoroughly. Filter sterilize. Warm to 45°–50°C.
Composition per liter:
Preparation of Medium: Add components, ex-
Agar ..................................................................20.0g Proteose peptone ...............................................20.0g Pancreatic digest of casein ..................................5.0g NaCl ....................................................................5.0g Yeast extract........................................................5.0g Egg yolk emulsion, 50%............................... 80.0mL pH 7.0 ± 0.2 at 25°C
cept egg yolk emulsion, to distilled/deionized water and bring volume to 980.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile egg yolk emulsion. Mix thoroughly. Pour into sterile Petri dishes. Allow plates to dry at 35°C for 24h.
Egg Yolk Emulsion, 50%: Composition per 80.0mL: Chicken egg yolks...................................... 2 or more NaCl (0.85% solution) .................................. 40.0mL
Preparation of Egg Yolk Emulsion, 50%: Wash fresh eggs wtih stiff brush and drain. Soak eggs in 70% ethanol for 1 hour. Crack eggs aseptically and separate yolks from whites. Drain contents of yolk sacs into sterile stoppered graduate cylinder and discard sacs. Measure 40.0mL of egg yolk emulsion and add 40.0mL of 0.85% NaCl solution. Mix thoroughly by inverting graduate cyliner. Warm to 45°–50°C.
Preparation of Medium: Add components, except egg yolk emulsion, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 80.0mL sterile egg yolk emulsion. Mix thoroughly. Pour into sterile Petri dishes. Allow plates to dry at ambient temperature for 2–3 days or at 35°C for 24h. Check plates for contamination before use.
Use: For the cultivation of Yersinia enterocolitica.
Use: For the cultivation of Yersinia enterocolitica.
Anaerobic LKV Blood Agar Composition per liter: Agar ..................................................................15.0g Pancreatic digest of casein................................13.0g Peptic digest of animal tissue ...........................10.0g NaCl....................................................................5.0g Yeast extract........................................................2.0g Glucose ...............................................................1.0g NaHSO3 ..............................................................0.1g Sheep blood, laked........................................ 50.0mL Antibiotic solution ........................................ 10.0mL Hemin solution................................................ 1.0mL Vitamin K1 solution ........................................ 1.0mL pH 7.1–7.8 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Antibiotic Solution: Composition per 10.0mL: Kanamycin......................................................0.075g Vancomycin .....................................................7.5mg
Preparation of Antibiotic Solution: Add com-
Anaerobic Egg Yolk Agar Composition per liter: Agar ..................................................................20.0g Proteose peptone ...............................................20.0g Pancreatic digest of casein ..................................5.0g NaCl ....................................................................5.0g
ponents to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Vitamin K1 Solution: Composition per 100.0mL: Vitamin K1 ..........................................................0.1g Ethanol.......................................................... 99.0mL
Anaerobic Oxalate Medium Preparation of Vitamin K1 Solution: Add vitamin K1 to 99.0mL of absolute ethanol. Mix thoroughly.
31
Solution B (Trace Elements Solution SL-10 ): Composition per liter:
20.0mL of 1N NaOH solution. Mix thoroughly. Bring volume to 100.0mL with distilled/deionized water.
FeCl2·4H2O .........................................................1.5g CoCl2·6H2O .................................................190.0mg MnCl2·4H2O ................................................100.0mg ZnCl2 ..............................................................70.0mg Na2MoO4·2H2O .............................................36.0mg NiCl2·6H2O ....................................................24.0mg H3BO3 ..............................................................6.0mg CuCl2·2H2O .....................................................2.0mg HCl (25% solution)....................................... 10.0mL
Preparation of Medium: Add components—ex-
Preparation of Solution B: Add FeCl2·4H2O to
Hemin Solution: Composition per 100.0mL: Hemin................................................................0.01g NaOH (1N solution)...................................... 20.0mL
Preparation of Hemin Solution: Add hemin to
cept sheep blood, antibiotic solution, and vitamin K1 solution—to distilled/deionized water and bring volume to 939.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 50.0mL of sterile sheep blood, 10.0mL of sterile antibiotic solution, and 1.0mL of sterile vitamin K1 solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
10.0mL of HCl solution. Mix thoroughly. Add distilled/deionized water and bring volume to 1.0L. Add remaining components. Mix thoroughly. Gas under 100% N2. Autoclave for 15 min at 15 psi pressure– 121°C.
Use: For the isolation and cultivation of anaerobic
Preparation of Solution C: Add NaHCO3 to dis-
Gram-negative microorganisms, expecially Bacteroides species.
Anaerobic Oxalate Medium Composition per 1011.0mL:
Solution C: Composition per 100.0mL: NaHCO3 ..............................................................5.0g tilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize. Gas under 80% N2 + 20% CO2.
Solution D: Composition per 20.0mL: Ammonium oxalate ............................................3.0g Yeast extract........................................................1.0g Sodium acetate..................................................0.41g
Solution A ................................................... 870.0mL Solution C ................................................... 100.0mL Solution D ..................................................... 20.0mL Solution E (Vitamin solution) ....................... 10.0mL Solution F...................................................... 10.0mL Solution B (Trace elements solution SL-10) .. 1.0mL pH 7.1–7.4 at 25°C
Preparation of Solution D: Add components to distilled/deionized water and bring volume to 20.0mL. Mix thoroughly. Gas under 100% N2. Autoclave for 15 min at 15 psi pressure–121°C.
Solution A: Composition per 870.0mL:
Solution E (Vitamin Solution): Composition per liter:
Na2SO4 ................................................................3.0g NaCl ....................................................................1.0g KCl......................................................................0.5g MgCl2·6H2O .......................................................0.4g NH4Cl .................................................................0.3g KH2PO4 ...............................................................0.2g CaCl2·2H2O.......................................................0.15g Resazurin .........................................................1.0mg
Preparation of Solution A: Add components to distilled/deionized water and bring volume to 870.0mL. Mix thoroughly. Gently heat and bring to boiling. Continue boiling for 3-4 min. Allow to cool to room temperature while gassing under 80% N2 + 20% CO2. Continue gassing until pH reaches below 6.0. Seal the flask under 80% N2 + 20% CO2. Autoclave for 15 min at 15 psi pressure–121°C.
Pyridoxine·HCl ..............................................10.0mg Calcium DL-pantothenate.................................5.0mg Lipoic acid .......................................................5.0mg Nicotinic acid...................................................5.0mg p-Aminobenzoic acid.......................................5.0mg Riboflavin ........................................................5.0mg Thiamine·HCl ..................................................5.0mg Biotin ...............................................................2.0mg Folic acid .........................................................2.0mg Vitamin B12 ......................................................0.1mg
Preparation of Solution E (Vitamin Solution): Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gas under 100% N2. Autoclave for 15 min at 15 psi pressure– 121°C.
32
Anaerobic Trypticase™ Soy Agar with Calf Blood
Solution F: Composition per 10.0mL: Na2S·9H2O..........................................................0.4g
Preparation of Solution F: Add Na2S·9H2O to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Gas under 100% N2. Autoclave for 15 min at 15 psi pressure–121°C. Preparation of Medium: Aseptically and anaerobically combine solution A with solution B, solution C, solution D, solution E, and solution F, in that order. Mix thoroughly. Anaerobically distribute into sterile tubes or flasks under 80% N2 + 20% CO2.
Use: For the cultivation of Clostridium oxalicum and Oxalobacter vibrioformis.
Anaerobic Trypticase™ Soy Agar with Calf Blood (ATCC Medium 1664) Composition per liter: Pancreatic digest of casein................................15.0g Agar ..................................................................15.0g Papaic digest of soybean meal ............................5.0g NaCl ....................................................................5.0g Calf blood, defibrinated .............................. 100.0mL pH 7.3 ± 0.2 at 25°C
Preparation of Medium: Add components, except bovine serum, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 100.0mL of bovine serum. Distribute into sterile tubes.
Use: For the isolation and cultivation of anaerobic microorganisms.
Andersen’s Pork Pea Agar Composition per 1685.0mL: Agar ..................................................................16.0g Peptone ...............................................................5.0g Pancreatic digest of casein..................................1.6g K2HPO4.............................................................1.25g Soluble starch......................................................1.0g Sodium thioglycolate ..........................................0.5g Pork infusion............................................... 800.0mL Thioglycolate agar ...................................... 660.0mL Pea infusion ................................................ 200.0mL NaHCO3 solution .......................................... 25.0mL pH 7.2 ± 0.2 at 25°C
Pork Infusion: Composition per liter:
Preparation of Medium: Add components, ex-
Pork, fresh lean ground...................................454.0g
cept calf blood, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Prepare medium anaerobically with 80% N2 + 10% CO2 + 10% H2. Gently heat while stirring and bring to boiling for 1 min. Autoclave for 15 min at 15 psi pressure– 121°C. Do not overheat. Cool to 45°–50°C. Aseptically add 100.0mL sterile, defibrinated calf blood. Pour into sterile Petri dishes.
Preparation of Pork Infusion: Add ground pork
Use: For the isolation and cultivation of fastidious as well as nonfastidious microorganisms. For the differentiation of Haemophilus species.
Anaerobic TVLS Medium Composition per liter: Pancreatic digest of casein................................17.0g Beef extract .........................................................7.5g Glucose ...............................................................6.0g Enzymatic hydrolysate of soybean meal ............3.0g Liver hydrolysate ................................................3.0g NaCl ....................................................................2.5g Na2SO3 ................................................................0.7g Sodium thioglycolate ..........................................0.5g L-Cysteine·HCl·H2O..........................................0.25g Agar ....................................................................0.1g Bovine serum .............................................. 100.0mL pH 7.3 ± 0.2 at 25°C
to distilled/deionized water and bring volume to 1.0L. Autoclave for 60 min at 0 psi pressure–100°C. Filter through two layers of cheesecloth. Cool to 4°C. Skim fat from surface. Warm to 25°C. Centrifuge at 5000 rpm for 10 min. Discard pellet.
Pea Infusion: Composition per 450.0mL: Green peas, fresh or frozen.............................454.0g Diatomaceous earth (celite) ..............................10.0g
Preparation of Pea Infusion: Add green peas to 450.0mL of distilled/deionized water. Blend until smooth. Autoclave for 60 min at 0 psi pressure– 100°C. Centrifuge at 5000 rpm for 10 min. Discard pellet. Clarify supernatant solution with diatomaceous earth (celite). Filter through Whatman #4 filter paper. Use filtrate solution.
Thioglycolate Agar: Composition per liter: Agar ................................................................20.75g Pancreatic digest of casein................................15.0g Glucose ...............................................................5.5g Yeast extract........................................................5.0g NaCl....................................................................2.5g L-Cystine .............................................................0.5g
Andrade’s Broth
33
Sodium thioglycolate ..........................................0.5g Resazurin .........................................................1.0mg pH 7.1 ± 0.2 at 25°C
Carbohydrate Solution: Composition per 100.0mL:
Preparation of Thioglycolate Agar: Add com-
Preparation of Carbohydrate Solution: Add
ponents to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C.
NaHCO3 Solution: Composition per 100.0mL: NaHCO3 ..............................................................5.0g
Preparation of NaHCO3 Solution: Add NaHCO3 to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Combine components, except NaHCO3 solution and thioglycolate agar. Mix thoroughly. Adjust pH to 7.2. Autoclave for 5 min at 15 psi pressure–121°C. While medium is still hot, add 25.0g of celite. Filter through Whatman #4 filter paper with suction. Autoclave for 12 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 25.0mL of sterile NaHCO3 solution. Mix thoroughly. Pour into sterile Petri dishes in 15.0mL volumes. Allow agar to solidify. Cover agar with 10.0mL of sterile, cooled thioglycolate agar.
Use: For the cultivation of mesophilic Clostridium species.
Andrade’s Carbohydrate Broth and Indicator Composition per liter: Pancreatic digest of gelatin ...............................10.0g NaCl ..................................................................10.0g Beef extract .........................................................3.0g Carbohydrate solution................................. 100.0mL Andrade’s indicator....................................... 10.0mL pH 7.2 ± 0.2 at 25°C
Source: This medium is available as a prepared medium from BD Diagnostic Systems, in tubes containing adonitol, arabinose, cellobiose, glucose, dulcitol, fructose, galactose, inositol, lactose, maltose, mannitol, raffinose, rhamnose, salicin, sorbitol, sucrose, trehalose, or xylose.
Andrade’s Indicator Composition per 26.0mL: NaOH (1N solution)...................................... 16.0mL Acid Fuchsin ....................................................0.21 g
Preparation of Andrade’s Indicator: Add Acid Fuchsin to NaOH solution and bring volume to 26.0mL with distilled/deionized water.
Carbohydrate..............................................5.0–10.0g carbohydrate to distilled/deionized water and bring volume to 100.0mL. For glucose, lactose, sucrose, and mannitol, add 10.0g to distilled/deionized water and bring volume to 100.0mL. For dulcitol, salicin, and other carbohydrates, add 5.0g to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except carbohydrate solution, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Cool. Aseptically add 100mL of sterile carbohydrate solution to 900mL of sterile medium. Mix thoroughly. Aseptically distribute into tubes or flasks. Alternately, prior to autoclaving, distribute 9.0mL volumes into test tubes containing inverted Durham tubes. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C. Add 1.0mL of sterile carbohydrate solution to each tube.
Caution: Acid Fuchsin is a potential carcinogen and care must be taken to avoid inhalation of the powdered dye and contact with the skin.
Use: For the determination of carbohydrate fermentation reactions of microorganisms, particularly members of the Enterobacteriaceae. A Durham tube is used to collect gas produced during the fermentation reaction. Acid production is indicated by a pink color.
Andrade’s Broth Composition per liter: Pancreatic digest of gelatin...............................10.0g NaCl....................................................................5.0g Beef extract.........................................................3.0g Andrade’s indicator....................................... 10.0mL Carbohydrate solution................................... 50.0mL pH 7.4 ± 0.2 at 25°C
Source: This medium is available as a prepared medium from BD Diagnostic Systems, in tubes containing adonitol, arabinose, cellobiose, dulcitol, fructose, galactose, glucose, inositol, lactose, maltose, mannitol, raffinose, rhamnose, salicin, sorbitol, sucrose, trehalose, or xylose.
Andrade’s Indicator Composition per 100.0mL: NaOH (1N solution)...................................... 16.0mL Acid Fuchsin......................................................0.1 g
Preparation of Andrade’s Indicator: Add Acid Fuchsin to NaOH solution and bring volume to 100.0mL with distilled/deionized water.
34
Anthracis Chromogenic Agar
Carbohydrate Solution: Composition per 100.0mL: Carbohydrate.....................................................10.0g
Preparation of Carbohydrate Solution: Add carbohydrate to distilled/deionized water and bring volume to 100.0mL. Adonitol, arabinose, cellobiose, dulcitol, fructose, galactose, glucose, inositol, lactose, maltose, mannitol, raffinose, rhamnose, salicin, sorbitol, sucrose, trehalose, xylose, or other carbohydrates may be used. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except carbohydrate solution, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute in 10.0mL volumes into test tubes containing inverted Durham tubes. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C. Add 0.5mL of sterile carbohydrate solution to each tube.
Caution: Acid Fuchsin is a potential carcinogen and care must be taken to avoid inhalation of the powdered dye and contact with the skin.
Use: For the determination of carbohydrate fermentation reactions of microorganisms, particularly members of the Enterobacteriaceae. A Durham tube is used to collect gas produced during the fermentation reaction. Acid production is indicated by a pink color.
Anthracis Chromogenic Agar Composition per liter:
colonies of Bacillus cereus/Bacillus thuringiensis after 20-24h at 35-37°C.
Antibiotic Medium 1 (Penassay Seed Agar) (Seed Agar)/(Agar Medium A) Composition per liter: Agar ..................................................................15.0g Pancreatic digest of gelatin.................................6.0g Pancreatic digest of casein..................................4.0g Yeast extract........................................................3.0g Beef extract.........................................................1.5g Glucose ...............................................................1.0g pH 6.6 ± 0.1 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For antibiotic assay testing, detection of antibiotics in milk, and determination of the antimicrobial effectiveness of antibiotics.
Antibiotic Medium 2 (Base Agar) (Penassay Base Agar)
Proprietary.
Composition per liter:
Source: This medium is available as a premixed powder from BIOSYNTH International, Inc. rections.
Agar ..................................................................15.0g Pancreatic digest of gelatin.................................6.0g Yeast extract........................................................3.0g Beef extract.........................................................1.5g pH 6.6 ± 0.1 at 25°C
Use: For the rapid identification and isolation of Ba-
Source: This medium is available as a premixed
Preparation of Medium: Per manufacturers di-
cillus anthracis based on the detection of phosphatidylcholine-specific phospholipase C activity by 5bromo-4-chloro-3-indoxyl-cholinphosphate hydrolysis. The medium incorporates chromogenic substrates for detecting specific enzyme activities in Bacillus anthracis, B. cereus, and B. thuringiensis. The enzymes targeted by the chromogenic medium are not present in other Bacillus species, allowing for specific isolation of these three Bacillus species. Inclusion of inhibitory compounds into the medium prevents the growth of environmental contaminants. The use of proprietary chromogenic substrates, X-IP and X-CP, allows for the differentiation of Bacillus anthracis from near-neighbors B. cereus and B. thuringiensis. Cream to pale teal-blue colored of Bacillus anthracis after 20-24h, teal-blue colonies of Bacillus anthracis after 36-48h at 35-37°C. Dark teal-blue
powder from BD Diagnostic Systems and Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes.
Use: For use as a base layer in antibiotic assay testing. Especially useful for the plate assay of bacitracin and penicillin G.
Antibiotic Medium 3 (Penassay Broth) Composition per liter: Pancreatic digest of gelatin.................................5.0g
Antibiotic Medium 7 K2HPO4 .............................................................3.68g NaCl ....................................................................3.5g Yeast extract........................................................1.5g Beef extract .........................................................1.5g KH2PO4 .............................................................1.32g Glucose ...............................................................1.0g pH 7.0 ± 0.05 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems and Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For antibiotic assay testing. Used for the serial dilution assay of penicillins and other antibiotics. Used in the turbidimetric assay of penicillin and tetracycline with Staphylococcus aureus. For the cultivation and maintenance of Staphylococcus aureus.
Antibiotic Medium 3 Plus Composition per liter: Agar ..................................................................15.0g Peptone................................................................5.0g K2HPO4 .............................................................3.68g NaCl ....................................................................3.5g Yeast extract........................................................2.5g Glucose .............................................................1.75g Beef extract .........................................................1.5g KH2PO4 .............................................................1.32g pH 7.0 ± 0.05 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For antibiotic assay testing and for the cultivation of Escherichia coli.
Antibiotic Medium 4 (Yeast Beef Agar) (Agar Medium C) Composition per liter: Agar ..................................................................15.0g Pancreatic digest of gelatin .................................6.0g Yeast extract........................................................3.0g Beef extract .........................................................1.5g Glucose ...............................................................1.0g pH 6.6 ± 0.05 at 25°C
35
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For antibiotic assay testing.
Antibiotic Medium 5 (Streptomycin Assay Agar with Yeast Extract) Composition per liter: Agar ..................................................................15.0g Pancreatic digest of gelatin.................................6.0g Yeast extract........................................................3.0g Beef extract.........................................................1.5g pH 7.9 ± 0.1 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems and Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes.
Use: For antibiotic assay testing. For the streptomycin assay using the cylinder plate technique and Bacillus subtilis as test organism.
Antibiotic Medium 6 Composition per liter: Pancreatic digest of casein................................17.0g NaCl....................................................................5.0g Papaic digest of soybean meal............................3.0g Glucose ...............................................................2.5g K2HPO4...............................................................2.5g MnSO4·H2O ......................................................0.03g pH 7.0 ± 0.1 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes.
Use: For antibiotic assay testing.
Antibiotic Medium 7 Composition per liter: Agar ..................................................................15.0g
36
Antibiotic Medium 8
Pancreatic digest of gelatin .................................6.0g Yeast extract........................................................3.0g Beef extract .........................................................1.5g pH 7.0 ± 0.1 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Adjust pH to 7.0. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes.
Use: For use as a base layer in antibiotic assay testing. Especially useful for the plate assay of bacitracin and penicillin G.
Antibiotic Medium 8 (Base Agar with Low pH) Composition per liter: Agar ..................................................................15.0g Pancreatic digest of gelatin .................................6.0g Yeast extract........................................................3.0g Beef extract .........................................................1.5g pH 5.9 ± 0.1 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes.
Use: For antibiotic assay testing. For use as the base agar and the seed agar in the plate assay of tetracycline. For use as the seed agar in the plate assay of vancomycin, mitomycin, and mithramycin.
Antibiotic Medium 9 (Polymyxin Base Agar) Composition per liter: Agar ..................................................................20.0g Pancreatic digest of casein................................17.0g NaCl ....................................................................5.0g Papaic digest of soybean meal ............................3.0g K2HPO4 ...............................................................2.5g Glucose ...............................................................2.5g pH 7.2 ± 0.1 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min
at 15 psi pressure–121°C. Pour into sterile Petri dishes.
Use: For antibiotic assay testing. For base agar for the plate assay of carbenicillin, colistimethate, and polymyxin B.
Antibiotic Medium 10 (Polymyxin Seed Agar) Composition per liter: Pancreatic digest of casein................................17.0g Agar ..................................................................12.0g Polysorbate 80 ..................................................10.0g NaCl....................................................................5.0g Papaic digest of soybean meal............................3.0g K2HPO4...............................................................2.5g Glucose ...............................................................2.5g pH 7.3 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes.
Use: For antibiotic assay testing. For seed agar for the plate assay of carbenicillin, colistimethate, and polymyxin B.
Antibiotic Medium 11 (Neomycin Assay Agar) Composition per liter: Agar ..................................................................15.0g Pancreatic digest of gelatin.................................6.0g Pancreatic digest of casein..................................4.0g Yeast extract........................................................3.0g Beef extract.........................................................1.5g Glucose ...............................................................1.0g pH 8.0 ± 0.1 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems and Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes.
Use: For antibiotic assay testing. For base agar and seed agar for the plate assay to test the effectiveness of neomycin sulfate, amoxicillin, ampicillin, clinda-
Antibiotic Medium 21 mycin, cyclacillin, erythromycin, gentamycin, neomycin, oleandomycin, and sisomycin.
Antibiotic Medium 12 Composition per liter: Agar ..................................................................25.0g Peptone..............................................................10.0g Glucose .............................................................10.0g NaCl ..................................................................10.0g Yeast extract........................................................5.0g Beef extract .........................................................2.5g pH 6.0 ± 0.1 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes.
Use: For antibiotic assay effectiveness testing.
Antibiotic Medium 13 (Sabouraud Liquid Broth, Modified) (Fluid Sabouraud Medium) Composition per liter: Glucose .............................................................20.0g Pancreatic digest of casein..................................5.0g Peptic digest of animal tissue..............................5.0g pH 5.7 ± 0.1 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes.
Use: For testing the effectivness of antibiotics on yeast and molds.
Antibiotic Medium 19 (Nystatin Assay Agar) Composition per liter: Agar ..................................................................23.5g Glucose .............................................................10.0g NaCl ..................................................................10.0g Pancreatic digest of gelatin .................................9.4g Yeast extract........................................................4.7g Beef extract .........................................................2.4g pH 6.1 ± 0.2 at 25°C
37
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes.
Use: For assaying the mycostatic activity of pharmaceutical preparations. For seed agar for the plate assay to test the effectiveness of nystatin, amphotericin B, and natamycin.
Antibiotic Medium 20 Composition per liter: Glucose ............................................................. 11.0g Pancreatic digest of casein................................10.0g Yeast extract........................................................6.5g Pancreatic digest of gelatin.................................5.0g K2HPO4.............................................................3.68g NaCl....................................................................3.5g Beef extract.........................................................1.5g KH2PO4.............................................................1.32g pH 6.6 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes.
Use: For assaying the mycostatic activity of pharmaceutical preparations.
Antibiotic Medium 21 Composition per liter: Glucose ............................................................. 11.0g Pancreatic digest of gelatin.................................5.0g K2HPO4.............................................................3.68g NaCl....................................................................3.5g Yeast extract........................................................1.5g Beef extract.........................................................1.5g KH2PO4.............................................................1.32g pH 6.6 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes.
Source: This medium is available as a premixed
Use: For assaying the mycostatic activity of pharma-
powder from BD Diagnostic Systems.
ceutical preparations.
38
Antibiotic Sulfonamide Sensitivity Test Agar
Antibiotic Sulfonamide Sensitivity Test Agar (ASS Agar) Composition per liter: Agar ..................................................................12.0g Proteose peptone ...............................................10.0g Beef extract .......................................................10.0g NaCl ....................................................................3.0g Glucose ...............................................................2.0g Na2HPO4 .............................................................2.0g Sodium acetate....................................................1.0g Adenine.............................................................0.01g Guanine.............................................................0.01g Uracil ................................................................0.01g Xanthine............................................................0.01g pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For testing the antimicrobial effectiveness of antibiotics and sulfonamides. For detecting the presence of antimicrobial substances in urine.
AOAC Letheen Broth (Association of Official Analytical Chemists Letheen Broth) Composition per liter: Peptic digest of animal tissue............................10.0g Polysorbate 80.....................................................5.0g NaCl ....................................................................5.0g Beef extract .........................................................5.0g Lecithin ...............................................................0.7g pH 7.0 ± 0.2 at 25°C
Agarose solution ................................................ 1.0L Fetal calf serum, inactivated ....................... 100.0mL pH 7.0 ± 0.2 at 25°C
Eagle’s Basal Medium: Composition per liter: HEPES (N-2-HydroxyethylpiperazineN´-2-ethanesulfonic acid) buffer ................9.53g NaCl....................................................................6.8g NaHCO3 ..............................................................2.2g Glucose ...............................................................1.0g KCl......................................................................0.4g CaCl2·2H2O ........................................................0.2g NaH2PO4 .........................................................0.125g MgSO4·7H2O ......................................................0.1g L-Isoleucine .....................................................0.026g L-Leucine ........................................................0.026g L-Lysine...........................................................0.026g L-Threonine .....................................................0.024g L-Valine .........................................................0.0235g L-Tyrosine .......................................................0.018g L-Arginine .....................................................0.0174g L-Phenylalanine.............................................0.0165g L-Cystine .........................................................0.012g L-Histidine........................................................8.0mg L-Methionine ....................................................7.5mg L-Tryptophan....................................................4.0mg Inositol .............................................................1.8mg Biotin ...............................................................1.0mg Calcium pantothenate ......................................1.0mg Choline chloride...............................................1.0mg Folic acid .........................................................1.0mg Nicotinamide....................................................1.0mg Pyridoxal·HCl ..................................................1.0mg Thiamine·HCl ..................................................1.0mg Riboflavin ........................................................0.1mg pH 7.2–7.4 at 25°C
Source: This medium is available as a premixed
Source: This medium is available as a premixed
powder from BD Diagnostic Systems.
powder from BD Diagnostic Systems.
Preparation of Eagle’s Basal Medium: Add
Preparation of Medium: Add components to
components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.0 with NaOH. Filter sterilize.
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes in 10.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C.
Agarose Solution: Composition per liter:
Use: For the determination of phenol coefficients of
Agarose .............................................................20.0g
disinfectant products containing cationic surface-active materials. Use according to Official Methods of Analysis of the Association of Official Analytical Chemists (AOAC).
Preparation of Agarose Solution: Add agarose to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Arenavirus Plaquing Medium Composition per liter: Eagle’s basal medium ........................................ 1.0L
Preparation of Medium: To 1.0L of sterile Eagle’s basal medium, aseptically add 1.0L of sterile, cooled agarose solution and 100.0mL of fetal calf serum. Mix thoroughly. Pour into sterile Petri dishes.
Arylsulfatase Agar Use: For the cultivation of animal tissue culture cells used for the growth of arenaviruses.
Arginine Broth Composition per liter: L-Arginine ...........................................................5.0g
Peptone or gelysate .............................................5.0g Yeast extract........................................................3.0g Glucose ...............................................................1.0g Bromcresol Purple ............................................0.02g pH 6.5 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH so that is will be 6.5 ± 0.2 after sterilization. Distribute into 16 × 150mm screwcapped tubes in 5.0mL volumes. Autoclave medium with loosely capped tubes for 10 min at 15 psi pressure– 121°C. Screw the caps on tightly for storage and after inoculation.
Use: For the cultivation and differentiation of bacteria based on their ability to decarboxylate the amino acid arginine. Bacteria that decarboxylate arginine turn the medium turbid purple.
Arginine Broth with NaCl Composition per liter: L-Arginine ...........................................................5.0g
Peptone or gelysate .............................................5.0g Yeast extract........................................................3.0g Glucose ...............................................................1.0g Bromcresol Purple ............................................0.02g pH 6.5 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH so that is will be 6.5 ± 0.2 after sterilization. Distribute into 16 × 150mm screwcapped tubes in 5.0mL volumes. Autoclave medium with loosely capped tubes for 10 min at 15 psi pressure– 121°C. Screw the caps on tightly for storage and after inoculation.
Use: For the cultivation and differentiation of Vibrio spp. based on their ability to decarboxylate the amino acid arginine. Bacteria that decarboxylate arginine turn the medium turbid purple.
Arginine Glucose Slants (AGS) Composition per liter: NaCl ..................................................................20.0g Agar ..................................................................13.5g Pancreatic digest of casein................................10.0g L-Arginine·HCl....................................................5.0g
39
Peptone ...............................................................5.0g Yeast extract........................................................3.0g Glucose ...............................................................1.0g Ferric ammonium citrate.....................................0.5g Na2S2O3·5H2O ....................................................0.3g Bromcresol Purple ............................................0.02g pH 6.8–7.0 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes. Autoclave for 12 min at 15 psi pressure–121°C. Allow tubes to cool in a slanted position.
Use: For the cultivation and differentation of Vibrio species.
Armstrong Fusarium Medium Composition per liter: Glucose .............................................................20.0g Ca(NO3)2·4H2O ..................................................8.4g KH2PO4.............................................................1.09g KCl....................................................................0.22g FeCl3 .................................................................0.2µg MnSO4 ..............................................................0.2µg ZnSO4 ...............................................................0.2µg
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
Use: For the cultivation of Fusarium species.
Arylsulfatase Agar (Wayne Sulfatase Agar) Composition per liter: Agar ..................................................................15.0g Na2HPO4 .............................................................2.5g L-Asparagine .......................................................1.0g KH2PO4...............................................................1.0g K2HPO4...............................................................1.0g Trisodium phenolphthalein sulfate ...................0.65g Pancreatic digest of casein..................................0.5g Ferric ammonium citrate...................................0.05g MgSO4·7H2O ....................................................0.01g CaCl2·2H2O .....................................................0.5mg ZnSO4·7H2O ....................................................0.1mg CuSO4 ..............................................................0.1mg Glycerol ........................................................ 10.0mL pH 7.0 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add glycerol to approximately 800.0mL of distilled/deionized water. Mix thoroughly. Add remaining components and
40
Ascospore Agar
bring volume to 1.0L with distilled/deionized water. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes. Autoclave for 15 min at 15 psi pressure–121°C. Cool tubes in an upright position.
Use: For the biochemical differentiation of species of Mycobacterium. Inoculate tubes with Mycobacterium cultures and incubate aerobically at 35°C for 3– 14 days. Add 0.5–1.0mL of 2N Na2CO3 to each tube and observe color change within 30 min. Development of a pink color is indicative of Mycobacterium fortuitum or Mycobacterium chelonae. Mycobacterium tuberculosis gives a negative reaction.
Ascospore Agar Composition per liter: Potassium acetate..............................................30.0g Yeast extract........................................................2.5g Glucose ...............................................................1.0g pH 6.4 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the enrichment of ascosporogenous yeasts and their production of ascospores.
ASM Medium Composition per 1001.2mL: Na2HPO4 ......................................................866.0mg NH4·Cl .........................................................535.0mg KH2PO4 ........................................................531.0mg K2SO4...........................................................174.0mg MgSO4·7H2O .................................................37.0mg CaCl2·2H2O....................................................7.35mg Trace elements solution .................................. 1.0mL FeSO4 solution ................................................ 0.2mL
Trace Elements Solution: Composition per liter: ZnSO4·7H2O ................................................288.0mg MnSO4·4H2O ...............................................224.0mg CuSO4·5H2O ................................................125.0mg KI ...................................................................83.0mg H3BO3 ............................................................61.8mg Na2MoO4·2H2O .............................................48.4mg CoCl2·6H2O ...................................................47.6mg H2SO4, 1M ...................................................... 1.0mL
Preparation of Trace Elements Solution: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C.
FeSO4 Solution: Composition per liter: FeSO4·7H2O ................................................278.0mg
Preparation
of FeSO4 Solution: Add FeSO4·7H2O to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. Preparation of Medium: Add components, except trace elements solution and FeSO4 solution, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Aseptically add 1.0mL of trace elements solution and 0.2mL of sterile FeSO4 solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation of Mycobacterium species.
Asparaginate Glycerol Agar Composition per liter: Agar ..................................................................15.0g Sodium asparaginate...........................................1.0g K2HPO4...............................................................1.0g Glycerol ........................................................ 10.0mL pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of Nocardia transvalensis.
Asparagine Broth Composition per liter: DL-Asparagine...................................................30.0g
K2HPO4...............................................................1.0g MgSO4·7H2O ......................................................0.5g pH 6.9–7.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix well until dissolved. Adjust pH to between 6.9 and 7.2. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For a presumptive test medium in the differentiation of nonfermentative Gram-negative bacteria, especially Pseudomonas aeruginosa.
Aspergillus Differential Medium Composition per liter: Agar ..................................................................15.0g Pancreatic digest of casein................................15.0g
AV Agar with Vitamins Yeast extract......................................................10.0g Ferric citrate........................................................0.5g
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes in 7.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C. Allow tubes to cool in a slanted position.
Use: For the cultivation and differentiation of Aspergillus flavus. Aspergillus flavus appears as bright orange colonies.
Aspergillus Medium
41
Egg yolk emulsion ...................................... 500.0mL Glycerol ........................................................ 10.0mL pH 6.5–7.0 at 25°C
Source: This medium is available as a prepared medium from BD Diagnostic Systems.
Egg Yolk Emulsion: Composition: Chicken egg yolks.................................................. 11 Whole chicken egg ..................................................1
Preparation of Egg Yolk Emulsion: Soak eggs with 1:100 dilution of saturated mercuric chloride solution for 1 min. Crack eggs and separate yolks from whites. Mix egg yolks with 1 chicken egg.
Composition per liter:
Preparation of Medium: Add components to
Agar ..................................................................15.0g NaNO3.................................................................6.0g Casamino acids ...................................................1.0g Peptone................................................................1.0g Yeast extract........................................................1.0g Adenine.............................................................0.15g Vitamin solution............................................ 10.0mL pH 6.0 ± 0.2 at 25°C
distilled/deionized water and bring volume to 1.0L. Distribute into tubes. Autoclave for 15 min at 15 psi pressure–121°C in a slanted position.
Vitamin Solution: Composition per 100.0mL: Biotin ................................................................0.01g Nicotinic acid ....................................................0.01g p-Aminobenzoic acid........................................0.01g Pyridoxine·HCl .................................................0.01g Riboflavin .........................................................0.01g Thiamine·HCl ...................................................0.01g
Preparation of Vitamin Solution: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Autoclave for 10 min at 15 psi pressure–121°C.
Preparation of Medium: Add components, except vitamin solution, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Adjust pH to 6.0. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C. Aseptically add 10.0mL of sterile vitamin solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation and maintenance of Aspergillus spp.
ATS Medium (American Trudeau Society Medium) Composition per liter: Potato ................................................................20.0g Malachite Green..................................................0.2g
Use: For the isolation and cultivation of Mycobacterium species other than Mycobacterium leprae. Especially useful for the detection of Mycobacterium tuberculosis from clinical specimens such as cerebrospinal fluid, pleural fluid, and tissues.
AV Agar with Vitamins Composition per liter: Agar ..................................................................15.0g Glucose ...............................................................1.0g Glycerol ..............................................................1.0g L-Arginine ...........................................................0.3g K2HPO4...............................................................0.3g NaCl....................................................................0.3g MgSO4·7H2O ......................................................0.2g Vitamin solution.......................................... 100.0mL Trace salts solution ......................................... 1.0mL
Vitamin Solution: Composition per 100.0mL: p-Aminobenzoic acid.......................................0.5mg Calcium pantothenate ......................................0.5mg HCl...................................................................0.5mg Inositol .............................................................0.5mg Niacin...............................................................0.5mg Pyridoxine........................................................0.5mg Ribovlavin........................................................0.5mg Thiamine·HCl ..................................................0.5mg Biotin .............................................................0.25mg
Preparation of Vitamin Solution: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
Trace Salts Solution: Composition per liter: FeSO4·7H2O......................................................10.0g CuSO4·5H2O .......................................................1.0g
42
Avian Mycoplasma Agar
MnSO4·7H2O ......................................................1.0g ZnSO4·7H2O .......................................................1.0g
Phenol Red Solution: Composition per 20.0mL:
Preparation of Trace Salts Solution: Add com-
Phenol Red........................................................0.02g
ponents to distilled/deionized water and bring volume to 1.0L. Mix thoroughly.
Preparation of Phenol Red Solution: Add Phe-
Preparation of Medium: Add components, ex-
nol Red to distilled/deionized water and bring volume to 20.0mL. Mix thoroughly. Filter sterilize.
cept vitamin solution, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 100.0mL of sterile vitamin solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Glucose Solution: Composition per 10.0mL:
Use: For the isolation and cultivation of Actinoma-
Arginine Solution: Composition per 10.0mL:
dura species, Actinopolyspora species, Excellospora species, and Microspora species.
Avian Mycoplasma Agar Composition per liter: Agar, not inhibitory to mycoplasmas................10.0g PPLO broth without Crystal Violet............. 700.0mL Swine or horse serum, heat inactivated at 56°C for 30 min. ............................... 150.0mL Fresh yeast extract solution......................... 100.0mL Phenol Red solution ...................................... 20.0mL Glucose solution ........................................... 10.0mL Arginine solution .......................................... 10.0mL NAD solution................................................ 10.0mL
PPLO Broth without Crystal Violet: Composition per 700.0mL: Beef heart, infusion from ................................175.0g Peptone................................................................7.0g NaCl ....................................................................3.5g
Source: PPLO broth without Crystal Violet is available as a premixed powder from BD Diagnostic Systems.
Preparation of PPLO Broth without Crystal Violet: Add components to distilled/deionized water and bring volume to 700.0mL. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C. Beef heart for infusion may be substituted; 100.0g of beef heart for infusion is equivalent to 500.0g of fresh heart tissue.
Fresh Yeast Extract Solution: Composition per 100.0mL: Baker’s yeast, live, pressed, starch-free............25.0g
Preparation of Fresh Yeast Extract Solution: Add the live Baker’s yeast to 100.0mL of distilled/ deionized water. Autoclave for 90 min at 15 psi pressure–121°C. Allow to stand. Remove supernatant solution. Adjust pH to 6.6–6.8.
Glucose ...............................................................1.0g
Preparation of Glucose Solution: Add glucose to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Arginine ..............................................................1.0g
Preparation of Arginine Solution: Add arginine to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
NAD Solution: Composition per 10.0mL: NAD....................................................................0.1g
Preparation of NAD Solution: Add NAD to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add 10.0g of agar to 700.0mL of PPLO broth without Crystal Violet. Gently heat to boiling with frequent mixing. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Warm other components to 50°–55°C using a water bath. Aseptically combine all components. Mix thoroughly. Pour into sterile Petri dishes or sterile tubes.
Use: For the cultivation and maintenance of Mycoplasma species.
Avian Mycoplasma Broth Composition per liter: PPLO broth without Crystal Violet............. 700.0mL Swine or horse serum, heat inactivated at 56°C for 30 min................................ 150.0mL Fresh yeast extract solution ........................ 100.0mL Phenol Red solution...................................... 20.0mL Glucose solution ........................................... 10.0mL Arginine solution .......................................... 10.0mL NAD solution................................................ 10.0mL
PPLO Broth without Crystal Violet: Composition per 700.0mL: Beef heart, infusion from................................175.0g Peptone ...............................................................7.0g NaCl....................................................................3.5g
Azide Blood Agar with Crystal Violet
43
Source: PPLO broth without Crystal Violet is avail-
Peptic digest of animal tissue .............................5.0g
able as a premixed powder from BD Diagnostic Systems.
NaCl....................................................................5.0g
Preparation of PPLO Broth without Crystal Violet: Add components to distilled/deionized water
NaN3 ...................................................................0.2g
and bring volume to 700.0mL. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C. Beef heart for infusion may be substituted; 100.0g of beef heart for infusion is equivalent to 500.0g of fresh heart tissue.
Fresh Yeast Extract Solution: Composition per 100.0mL: Baker’s yeast, live, pressed, starch-free............25.0g
Preparation of Fresh Yeast Extract Solution: Add the live Baker’s yeast to 100.0mL of distilled/ deionized water. Autoclave for 90 min at 15 psi pressure–121°C. Allow to stand. Remove supernatant solution. Adjust pH to 6.6–6.8.
Phenol Red Solution: Composition per 20.0mL: Phenol Red........................................................0.02g
Preparation of Phenol Red Solution: Add Phenol Red to distilled/deionized water and bring volume to 20.0mL. Mix thoroughly. Filter sterilize.
Glucose Solution: Composition per 10.0mL: Glucose ...............................................................1.0g
Preparation of Glucose Solution: Add glucose
Beef extract.........................................................3.0g Sheep blood, defibrinated ............................. 50.0mL pH 7.2 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems and Oxoid Unipath.
Caution: Sodium azide is toxic. Azides also react with metals and disposal must be highly diluted.
Preparation of Medium: Add components, except sheep blood, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45–50°C. Aseptically add 50.0mL of sterile defibrinated sheep blood. Pour into sterile Petri dishes or distribute into sterile tubes. Allow tubes to cool in a slanted position.
Use: For the isolation and differentiation of streptococci and staphylococci from specimens containing mixed flora.
Azide Blood Agar with Crystal Violet (Packer’s Agar)
to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Composition per liter:
Arginine Solution: Composition per 10.0mL:
Pancreatic digest of casein..................................5.0g
Arginine ..............................................................1.0g
Preparation of Arginine Solution: Add arginine to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
NAD Solution: Composition per 10.0mL:
Agar ..................................................................15.0g Peptic digest of animal tissue .............................5.0g NaCl....................................................................5.0g Beef extract.........................................................3.0g NaN3 ...................................................................0.9g Crystal Violet ...................................................2.0mg Sheep blood, defibrinated ............................. 50.0mL
NAD....................................................................0.1g
pH 7.2 ± 0.2 at 25°C
Preparation of NAD Solution: Add NAD to dis-
Caution: Sodium azide is toxic. Azides also react
tilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
with metals and disposal must be highly diluted.
Preparation of Medium: Aseptically combine components. Distribute into sterile tubes or flasks.
Use: For the cultivation and maintenance of Mycoplasma species.
Azide Blood Agar Composition per liter: Agar ..................................................................15.0g Pancreatic digest of casein..................................5.0g
Preparation of Medium: Add components, except sheep blood, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 50.0mL of sterile defibrinated sheep blood. Pour into sterile Petri dishes or distribute into sterile tubes. Allow tubes to cool in a slanted position.
Use: For the isolation of Streptococcus pneumoniae and Erysipelothrix rhusiopathiae.
44
Azide Broth
Azide Broth (Azide Glucose Broth) (Azide Dextrose Broth) Composition per liter: Pancreatic digest of casein................................15.0g Glucose ...............................................................7.5g NaCl ....................................................................7.5g Beef extract .........................................................4.5g NaN3 ...................................................................0.2g pH 7.2 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Caution: Sodium azide is toxic. Azides also react with metals and disposal must be highly diluted.
Preparation of Medium: Add components to
B Broth (Medium for Ureaplasma) Composition per 100.25mL: Yeast extract........................................................0.1g GHL (Glycyl-L-histidyl-L-lysine).....................2.0µg PPLO broth without Crystal Violet............... 50.0mL Horse serum, not inactivated ........................ 10.0mL Bromthymol Blue (0.4% solution) ................. 1.0mL Urea solution................................................. 0.25mL pH 6.0 ± 0.2 at 25°C
PPLO Broth without Crystal Violet: Composition per 50.0mL: Beef heart, infusion from..................................1.62g Peptone .............................................................0.32g NaCl..................................................................0.16g
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Prepare double-strength broth for samples larger than 1.0mL.
Source: PPLO broth without Crystal Violet is avail-
Use: Used in the multiple-tube technique as a pre-
ter and bring volume to 50.0mL. Mix thoroughly.
sumptive test for the presence of fecal streptococci.
Azide Medium Composition per liter: Peptone..............................................................10.0g K2HPO4 ..............................................................5.0g Glucose ...............................................................5.0g NaCl ....................................................................5.0g Yeast extract........................................................3.0g KH2PO4 ..............................................................2.0g NaN3 .................................................................0.25g Bromcresol Purple solution ............................ 2.0mL pH 7.2 ± 0.2 at 25°C
Bromcresol Purple Solution: Composition per 10.0mL: Bromcresol Purple ............................................0.16g Ethanol .......................................................... 10.0mL
Preparation of Bromcresol Purple Solution: Add Bromcresol Purple to ethanol and bring volume to 10.0mL. Mix thoroughly.
Caution: Sodium azide is toxic. Azides also react
able as a premixed powder from BD Diagnostic Systems.
Preparation of PPLO Broth without Crystal Violet: Add components to distilled/deionized waUrea Solution: Composition per 10.0mL: Urea.....................................................................1.0g
Preparation of Urea Solution: Add urea to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components—except GHL, urea solution, and horse serum—to double glass-distilled water and bring volume to 90.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 50°–55°C. To 90.0mL of the sterile medium, aseptically add 2.0µg of GHL, 10.0mL of horse serum, and 0.25mL of sterile urea solution. Mix thoroughly. Aseptically distribute into tubes or flasks.
Use: For the cultivation and maintenance of Ureaplasma urealyticum and other Ureaplasma species.
Bacillus cereus Medium (BCM)
with metals and disposal must be highly diluted.
Composition per 110.0mL:
Preparation of Medium: Add components to
Agar ....................................................................2.0g D-Mannitol ..........................................................1.0g (NH4)2PO4 ..........................................................0.1g KCl....................................................................0.02g MgSO4·7H2O ....................................................0.02g Yeast extract......................................................0.02g
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of Streptococcus species and Staphylococcus species.
Bacillus Medium
45
Bromcresol Purple ...........................................4.0mg Egg yolk emulsion, 20%............................... 10.0mL pH 7.0 ± 0.2 at 25°C
Preparation of Polymyxin B Solution: Add
Egg Yolk Emulsion, 20%: Composition per 100.0mL:
Preparation of Medium: Add components, ex-
Chicken egg yolks..................................................11 Whole chicken egg...................................................1 NaCl (0.9% solution) .................................... 80.0mL
Preparation of Egg Yolk Emulsion, 20%: Soak eggs with 1:100 dilution of saturated mercuric chloride solution for 1 min. Crack eggs and separate yolks from whites. Mix egg yolks with 1 chicken egg. Measure 20.0mL of egg yolk emulsion and add to 80.0mL of 0.9% NaCl solution. Mix thoroughly. Filter sterilize. Warm to 45°–50°C.
Preparation of Medium: Add components—except egg yolk emulsion, 20%—to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 10.0mL of sterile egg yolk emulsion, 20%. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation of Bacillus cereus.
Bacillus cereus Selective Agar Base Composition per liter: Agar ..................................................................15.0g Sodium pyruvate ...............................................10.0g Mannitol............................................................10.0g Na2HPO4 .............................................................2.5g NaCl ....................................................................2.0g Peptone................................................................1.0g KH2PO4 .............................................................0.25g Bromthymol Blue .............................................0.12g MgSO4·7H2O ......................................................0.1g Egg yolk emulsion ........................................ 25.0mL Polymyxin B solution ................................... 10.0mL pH 7.2 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath. Egg Yolk Emulsion: Composition: Chicken egg yolks..................................................11 Whole chicken egg...................................................1
Preparation of Egg Yolk Emulsion: Soak eggs
Polymyxin B to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. cept egg yolk emulsion and polymyxin B solution, to distilled/deionized water and bring volume to 965.0mL. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C. Aseptically add sterile polymyxin B and 25.0mL of sterile egg yolk emulsion. Mix thoroughly. Pour into sterile Petri dishes or leave in tubes.
Use: For the selection and presumptive identification of Bacillus cereus. Also for the isolation and enumeration of these bacteria. Bacillus cereus grows as moderate-sized (5mm) crenated colonies, which are turquoise, surrounded by a precipitate of egg yolk, which is also turquoise.
Bacillus Medium Composition per liter: Agar ..................................................................25.0g Peptone ...............................................................6.0g Pancreatic digest of casein..................................3.0g Yeast extract........................................................3.0g Beef extract.........................................................1.5g MnSO4·4H2O ....................................................1.0µg pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation of Bacillus species.
Bacillus Medium Composition per liter: (NH4)2HPO4........................................................1.0g MgSO4·7H2O ......................................................0.2g KCl......................................................................0.2g Yeast extract........................................................0.2g Glucose solution ........................................... 50.0mL Bromcresol Purple solution .......................... 15.0mL pH 7.0 ± 0.2 at 25°C
with 1:100 dilution of saturated mercuric chloride solution for 1 min. Crack eggs and separate yolks from whites. Mix egg yolks with 1 chicken egg.
Glucose Solution: Composition per 100.0mL:
Polymyxin B Solution: Composition per 10.0mL:
Preparation of Glucose Solution: Add glucose to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Polymyxin B ..............................................100,000U
Glucose .............................................................10.0g
46
Bacillus Medium
Preparation of Medium: Add components, except glucose solution, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute 9.5mL volumes into test tubes that contain an inverted Durham tube. Autoclave for 20 min at 15 psi pressure–121°C. Cool to 25°C. Aseptically add 0.5mL of sterile glucose to each tube. Mix thoroughly.
Use: For cultivation and differentiation of Bacillus species based on acid and gas production from glucose.
Bacillus Medium (ATCC Medium 455)
Papaic digest of soybean meal............................5.0g NaCl....................................................................5.0g Esculin ................................................................1.0g Ferric ammonium citrate.....................................0.5g Gentamicin solution........................................ 2.5mL Hemin solution................................................ 2.5mL Vitamin K1 solution ........................................ 1.0mL pH 7.0 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Gentamicin Solution: Composition per 10.0mL:
Composition per liter:
Gentamicin.......................................................0.4mg
Soluble starch....................................................30.0g Agar ..................................................................20.0g Polypeptone ........................................................5.0g Yeast extract........................................................5.0g
Preparation of Gentamicin Solution: Add
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Swirl medium to resuspend starch. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation of amylase-producing microorganisms.
Bacillus Medium (ATCC Medium 552) Composition per liter: Peptone..............................................................10.0g Lactose ................................................................5.0g NaCl ....................................................................5.0g Beef extract .........................................................3.0g K2HPO4 ...............................................................2.0g pH 7.2 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation and maintenance of Bacillus species.
Bacteroides Bile Esculin Agar (BBE Agar) Composition per liter: Oxgall................................................................20.0g Pancreatic digest of casein................................15.0g Agar ..................................................................15.0g
gentamicin to 10.0mL of distilled/deionized water. Mix thoroughly. Filter sterilize.
Hemin Solution: Composition per 100.0mL: Hemin .................................................................0.5g NaOH (1N solution)...................................... 10.0mL
Preparation of Hemin Solution: Add components to 100.0mL of distilled/deionized water. Mix thoroughly. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C.
Vitamin K1 Solution: Composition per 100.0mL: Vitamin K1 ..........................................................1.0g Ethanol.......................................................... 99.0mL
Preparation of Vitamin K1 Solution: Add vitamin K1 to 99.0mL of absolute ethanol. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except hemin solution, gentamicin solution, and vitamin K1 solution, to distilled/deionized water and bring volume to 994.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 2.5mL of sterile hemin solution, 2.5mL of sterile gentamicin solution, and 1.0mL of sterile vitamin K1 solution.
Use: For the selection and presumptive identification of the Bacteriodes fragilis group. For the differentiation of Bacteroides species based on the hydrolysis of esculin and presence of catalase. After incubation for 48 hr, bacteria of the Bacteroides fragilis group appear as gray, circular, raised colonies larger than 1.0mm. Esculin hydrolysis is indicated by the presence of a blackened zone around the colonies.
Baird-Parker Agar
BAF Agar
47
Baird-Parker Agar
Composition per liter:
Composition per liter:
Glucose .............................................................30.0g Agar ..................................................................15.0g Peptone................................................................2.0g KH2PO4 ...............................................................0.5g MgSO4·7H2O ......................................................0.5g Yeast extract........................................................0.2g CaCl2·2H2O..................................................100.0mg FeCl3·6H2O ....................................................10.0mg MnSO4 .............................................................5.0mg ZnSO4·7H2O ....................................................1.0mg Folic acid...................................................... 100.0µg Inositol ........................................................... 50.0µg Thiamine·HCl ................................................ 50.0µg Biotin ............................................................... 1.0µg pH 5.8 ± 0.2 at 25°C
Agar ..................................................................17.0g Glycine..............................................................12.0g Sodium pyruvate...............................................10.0g Pancreatic digest of casein................................10.0g Beef extract.........................................................5.0g LiCl .....................................................................5.0g Yeast extract........................................................1.0g pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Gently heat and bring to boiling. Adjust pH to 5.8. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation of a wide variety of bacteria.
BAGG Broth (Buffered Azide Glucose Glycerol Broth) Composition per liter: Pancreatic digest of casein................................10.0g Peptic digest of animal tissue............................10.0g Glucose ...............................................................5.0g NaCl ....................................................................5.0g K2HPO4 ...............................................................4.0g KH2PO4 ...............................................................1.5g NaN3 ...................................................................0.5g Bromcresol Purple ..........................................0.015g Glycerol .......................................................... 5.0mL pH 6.9 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Source: This medium is available as a premixed powder from Oxoid Unipath and BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Pour into sterile Petri dishes.
Use: Used as a base for the preparation of egg-tellurite-glycine-pyruvate agar for the selective isolation and enumeration of coagulase-positive staphylococci.
Baird-Parker Agar Composition per liter: Agar ..................................................................17.0g Glycine..............................................................12.0g Sodium pyruvate...............................................10.0g Pancreatic digest of casein................................10.0g Beef extract.........................................................5.0g LiCl .....................................................................5.0g Yeast extract........................................................1.0g Sulfamethazine solution................................ 10.0mL pH 7.0 ± 0.2 at 25°C
Sulfamethazine Solution: Composition per 10.0mL: Sulfamethazine .................................................0.05g
Preparation of Sulfamethazine Solution: Add
Caution: Sodium azide is toxic. Azides also react
sulfamethazine to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
with metals and disposal must be highly diluted.
Preparation of Medium: Add components, except
Preparation of Medium: Add 5.0mL of glycerol to 900.0mL of distilled/deionized water. Add remaining components and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes in 10.0mL volumes. Autoclave for 15 min at 10 psi pressure–116°C.
sulfamethazine solution, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile sulfamethazine solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation of fecal streptococci from a
Use: Used as a base for the preparation of egg-tellu-
variety of clinical specimens. It is recommended for qualitative presumptive and confirmatory tests for fecal streptococci.
rite-glycine-pyruvate agar for the selective isolation and enumeration of coagulase-positive staphylococci.
48
Baird-Parker Agar, Supplemented
Baird-Parker Agar, Supplemented Composition per liter: Agar ..................................................................17.0g Glycine..............................................................12.0g Sodium pyruvate ...............................................10.0g Pancreatic digest of casein................................10.0g Beef extract .........................................................5.0g LiCl .....................................................................5.0g Yeast extract........................................................1.0g RPF supplement.......................................... 100.0mL pH 7.0 ± 0.2 at 25°C
RPF Supplement: Composition per 100.0mL: Bovine fibrinogen .............................................3.75g Trypsin inhibitor ............................................25.0mg K2TeO3 ...........................................................25.0mg Rabbit plasma ............................................... 25.0mL
Caution: Potassium tellurite is toxic. Preparation of RPF Supplement: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except RPF supplement, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 100.0mL of filter-sterilized RPF supplement. Mix thoroughly but gently. Pour into sterile Petri dishes.
Use: For the selective isolation and enumeration of coagulase-positive staphylococci. For the differentiation and identification of staphylococci on the basis of their ability to coagulate plasma. Colonies surrounded by an opaque zone of coagulated plasma are diagnostic for Staphylococcus aureus.
Baird-Parker Medium Composition per liter: Agar ..................................................................20.0g Glycine..............................................................12.0g Sodium pyruvate ...............................................10.0g Pancreatic digest of casein................................10.0g Beef extract .........................................................5.0g LiCl·6H2O...........................................................5.0g Yeast extract........................................................1.0g EY tellurite enrichment................................. 50.0mL pH 7.0 ± 0.2 at 25°C
EY Tellurite Enrichment: Composition per 100.0mL: Chicken egg yolks..................................................10 K2TeO3 ..............................................................0.15g NaCl (0.9% solution) .................................... 50.0mL
Preparation of EY Tellurite Enrichment: Soak eggs with 1:100 dilution of saturated mercuric chloride solution for 1 min. Crack 11 eggs and separate yolks from whites. Mix egg yolks. Measure 30.0mL of egg yolk emulsion and add to 70.0mL of 0.9% NaCl solution. Mix thoroughly. Add 0.15g K2TeO3. Filter sterilize. Warm to 45°–50°C.
Caution: Potassium tellurite is toxic. Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components, except EY tellurite enrichment, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 48°–50°C. Aseptically add 50.0mL of sterile EY tellurite enrichment. Mix thoroughly. Pour into sterile Petri dishes. The medium must be densely opqaue. Dry plates before use. Plates can be stored for up to 5 days at 20– 25°C before use.
Use: For the selective isolation and enumeration of coagulase-positive staphylococci.
Balamuth Medium Composition per 200.0mL: Dehydrated egg yolk.........................................36.0g Dried liver concentrate .......................................1.0g Rice starch ..........................................................0.2g Potassium phosphate buffer, pH 7.5 ........... 125.0mL NaCl solution .............................................. 125.0mL pH 7.3 ± 0.2 at 25°C
NaCl Solution Composition per 200.0mL: NaCl....................................................................1.6g
Preparation of NaCl Solution: Add NaCl to distilled/deionized water and bring volume to 200.0mL. Mix thoroughly.
Potassium Phosphate Buffer, 0.067M Composition per 200.0mL: K2HPO4 (1M solution).................................... 8.6mL KH2PO4 (1M solution).................................. 4.66mL
Preparation of Potassium Phosphate Buffer: Combine the K2HPO4 and KH2PO4 solutions. Bring volume to 200.0mL with distilled/deionized water. Adjust pH to 7.5.
Preparation of Medium: Add dehydrated egg yolk to 36.0mL of distilled/deionized water. Add 125.0mL of 0.8% NaCl. Mix thoroughly in a blender. Heat in a covered, double boiler until infusion reaches 80°C and maintain at this temperature for 20 min. Add 20.0mL of distilled/deionized H2O. Filter
BCM Bacillus cereus Group Plating Medium through a layer of cheesecloth. To 90–100.0mL of filtrate add 0.8% NaCl solution to bring volume to 125.0mL. Autoclave for 20 min at 15 psi pressure– 121°C. Cool to 4°C. Filter. To filtrate, add an equal volume of 0.067M potassium phosphate buffer, pH 7.5. Add 1.0g of dried liver concentrate. Mix thoroughly. Distribute into tubes or flasks in 10.0mL volumes. Autoclave for 20 min at 15 psi pressure–121°C. Prior to inoculation, add 0.01g of rice starch to each tube.
Use: For the cultivation and maintenance of Entamoeba histolytica.
Basal Synthetic Medium Composition per liter: L-Glutamic
acid .................................................20.0g (NH4)2SO4...........................................................4.0g K2HPO4 .............................................................1.88g KH2PO4 .............................................................0.57g MgSO4·7H2O ......................................................0.2g Salt solution .................................................. 10.0mL
Salt Solution: Composition per liter: FeCl3·6H2O .........................................................0.6g MnCl2·4H2O .......................................................0.6g ZnCl2 ...................................................................0.6g CuSO4·5H2O .......................................................0.6g CaCl2·2H2O.........................................................0.6g NaCl ....................................................................0.6g
Preparation of Salt Solution: Add components to 1.0L of distilled/deionized water. Mix thoroughly.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation and maintenance of Acinetobacter lwoffii.
Basic Cultivation Medium Composition per liter: Yeast extract......................................................10.0g Glucose ...............................................................5.0g (NH4)2PO4...........................................................1.5g K2HPO4 ...............................................................1.0g MgSO4·7H2O ......................................................0.2g Fe2(SO4)3·5H2O ................................................0.01g ZnSO4·7H2O ...................................................0.002g pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L.
49
Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of a wide variety of microorganisms.
Basic Mineral Medium Composition per liter: NH4NO3 ..............................................................2.5g Na2HPO4·2H2O...................................................1.0g MgSO4·7H2O ......................................................0.5g Fe(SO4)3·5H2O .................................................0.01g Co(NO3)2·6H2O ..............................................0.005g CaCl2·2H2O .....................................................1.0mg KH2PO4............................................................0.5mg MnSO4·2H2O ...................................................0.1mg (NH4)6Mo7O24·4H2O .......................................0.1mg
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: To supply the mineral nutrients necessary for the cultivation of a wide variety of microorganisms. Various carbon sources can be added as sterilized solutions for testing carbon utilization capabilities.
BC Motility Medium (Bacillus cereus Motility Medium) Composition per liter: Pancreatic digest of casein................................10.0g Glucose ...............................................................5.0g Agar ....................................................................3.0g Na2HPO4 .............................................................2.5g Yeast extract........................................................2.5g pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes in 2.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation and observation of motility of Bacillus cereus.
BCM Bacillus cereus Group Plating Medium Composition per liter: Proprietary
Source: This medium is available from Biosynth International, Inc.
Use: For detection of Bacillus cereus. The medium contains 5-bromo-4-chloro-3-indoxyl-myoinositol1-phosphate, which changes from colorless to tur-
50
BCM O157:H7(+) Plating Medium
quoise upon enzymatic cleavage. B. cereus, B. mycoides, B. thuringiensis, and B. weihenstephanensis secrete phosphatidylinositol phospholipase C and so grow as turquoise colonies with species-specific morphologies.
BCM O157:H7(+) Plating Medium Composition per liter: Proprietary
Source: This medium is available from Biosynth International, Inc.
Use: For detection of this highly pathogenic EHEC serovar BCM O157:H7(+).
BCP D Agar (Bromcresol Purple Deoxycholate Agar) Composition per liter: Agar ..................................................................25.0g Lactose ..............................................................10.0g Sucrose..............................................................10.0g Pancreatic digest of casein..................................7.5g Thiopeptone ........................................................7.5g NaCl ....................................................................5.0g Yeast extract........................................................2.0g Sodium citrate .....................................................2.0g Sodium deoxycholate..........................................1.0g Bromcresol Purple ............................................0.02g pH 7.2 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Pour into sterile Petri dishes without sterilization. Do not autoclave. Use the same day.
Use: For the isolation, cultivation, and differentiation of Gram-negative enteric bacilli. For the isolation, cultivation, and identification of microorganisms from fecal specimens. For the isolation and cultivation of Salmonella, Shigella, and other nonlactose- and nonsucrose-fermenting microorganisms. Nonlactose/nonsucrose fermenting microorganisms appear as colorless or blue colonies. Lactose/sucrose-fermenting microorganisms, such as coliform bacteria, appear as yellowopaque white colonies surrounded by a zone of precipitated deoxycholate.
BCP DCLS Agar (Bromcresol Purple Deoxycholate Citrate Lactose Sucrose Agar) Composition per liter: Agar ..................................................................14.0g Sodium citrate ...................................................10.0g Lactose ................................................................7.5g
Sucrose................................................................7.5g Pancreatic digest of casein..................................7.5g Peptone ...............................................................7.5g NaCl....................................................................5.0g Na2S2O3·5H2O ....................................................5.0g Yeast extract........................................................3.0g Meat extract ........................................................3.0g Sodium deoxycholate..........................................2.5g Bromcresol Purple ............................................0.02g pH 7.2 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Pour into sterile Petri dishes without sterilization. Do not autoclave. Use the same day.
Use: For the differential isolation of Gram-negative enteric bacilli. For the isolation and identification of microorganisms from fecal specimens. For the isolation of Salmonella, Shigella, and other nonlactoseand nonsucrose-fermenting microorganisms. Nonlactose/nonsucrose-fermenting microorganisms appear as colorless or blue colonies. Lactose/sucrosefermenting microorganisms, such as coliform bacteria, appear as yellow-opaque white colonies surrounded by a zone of precipitated deoxycholate.
BCYE Agar (BCYE Alpha Base) (Buffered Charcoal Yeast Extract Agar) Composition per liter: Agar ..................................................................15.0g Yeast extract......................................................10.0g ACES buffer (2-[(2-Amino-2-oxoethyl)amino]-ethane sulfonic acid) ......................10.0g Charcoal, activated .............................................2.0g α-Ketoglutarate...................................................1.0g L-Cysteine·HCl·H2O............................................0.4g Fe4(P2O7)3·9H2O...............................................0.25g pH 6.9 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components, except cysteine, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust medium to pH 6.9 with 1N KOH. Heat gently and bring to boil for 1 min. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 50°–55°C. Add 4.0mL of a 10% solution of L-cysteine·HCl·H2O that has been filter sterilized. Mix thoroughly. Pour into sterile Petri dishes with constant agitation to keep charcoal in suspension.
BCYE Medium, Diphasic Blood Culture Use: For the isolation, cultivation, and maintenance of Legionella pneumophila and other Legionella species.
BCYE Differential Agar (Buffered Charcoal Yeast Extract Differential Agar)
51
Charcoal, activated, acid washed........................4.0g KOH....................................................................2.8g α-Ketoglutarate...................................................1.0g L-Cysteine·HCl·H2O solution ....................... 10.0mL Fe4(P2O7)3·9H2O solution............................. 10.0mL L-Cysteine·HCl·H2O
Solution: Composition per 10.0mL:
Composition per liter:
L-Cysteine·HCl·H2O............................................0.4g
Agar ..................................................................15.0g Yeast extract......................................................10.0g ACES buffer (2-[(2-Amino-2-oxoethyl)amino]-ethane sulfonic acid) ......................10.0g Charcoal, activated..............................................2.0g α-Ketoglutarate...................................................1.0g L-Cysteine·HCl·H2O............................................0.4g Fe4(P2O7)3·9H2O...............................................0.25g Bromcresol Purple ............................................0.01g Bromthymol Blue .............................................0.01g pH 6.9 ± 0.2 at 25°C
Preparation of L-Cysteine·HCl·H2O Solution: Add L-cysteine·HCl·H2O to distilled/deionized
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components, except L-cysteine·HCl·H2O, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust medium to pH 6.9 with 1N KOH. Heat gently and bring to boil for 1 min. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Add 4.0mL of a 10% solution of L-cysteine·HCl·H2O that has been filter sterilized. Mix thoroughly. Pour into sterile Petri dishes with constant agitation to keep charcoal in suspension.
Use: For the isolation, cultivation, and maintenance of Legionella pneumophila and other Legionella species. For the presumptive differential identification of Legionella species based on colony color and morphology. Legionella pneumophila appears as light blue/green colonies. Legionella micdadei appears as blue/gray or dark blue colonies.
BCYE Medium, Diphasic Blood Culture (Buffered Charcoal Yeast Extract Medium, Diphasic Blood Culture) Composition per liter: Agar phase ......................................................... 1.0L Broth phase ........................................................ 1.0L pH 6.9 ± 0.2 at 25°C
Agar Phase: Composition per liter: Agar ..................................................................20.0g ACES buffer (2-[(2-Amino-2-oxoethyl)amino]-ethane sulfonic acid) ......................10.0g Yeast extract......................................................10.0g
water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Fe4(P2O7)3·9H2O Solution: Composition per 10.0mL: Fe4(P2O7)3·9H2O...............................................0.25g
Preparation of Fe4(P2O7)3·9H2O Solution:
Add Fe4(P2O7)3·9H2O to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Agar Phase: Add components, except L-cysteine·HCl·H2O solution and Fe4(P2O7)3 solution, to distilled/deionized water and bring volume to 980.0mL. Mix thoroughly. Adjust medium to pH 6.9 with 1N KOH. Heat gently and bring to boiling for 1 min. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Aseptically add the L-cysteine·HCl·H2O solution and Fe4(P2O7)3·9H2O solution. Mix thoroughly.
Broth Phase: Composition per liter: ACES buffer (2-[(2-Amino-2-oxoethyl)amino]-ethane sulfonic acid) ......................10.0g Yeast extract......................................................10.0g Charcoal, activated, acid washed........................4.0g KOH....................................................................2.4g α-Ketoglutarate...................................................1.0g Sodium polyaneolsulfonate ................................0.3g L-Cysteine·HCl·H2O solution ....................... 10.0mL Fe4(P2O7)3·9H2O solution............................. 10.0mL L-Cysteine·HCl·H2O
Solution: Composition per 10.0mL: L-Cysteine·HCl·H2O............................................0.4g
Preparation of L-Cysteine·HCl·H2O Solution: Add L-cysteine·HCl·H2O to distilled/deionized
water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Fe4(P2O7)3·9H2O Solution: Composition per 10.0mL: Fe4(P2O7)3·9H2O...............................................0.25g
Preparation of Fe4(P2O7)3·9H2O Solution:
Add Fe4(P2O7)3·9H2O to distilled/deionized water
52
BCYE Selective Agar with CCVC
and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Broth Phase: Add components, except L-cysteine·HCl·H2O solution and Fe4(P2O7)3 solution, to distilled/deionized water and bring volume to 980.0mL. Mix thoroughly. Adjust medium to pH 6.9 with 1N KOH. Heat gently and bring to boiling for 1 min. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50–55°C. Aseptically add the cysteine·HCl·H2O solution and Fe4(P2O7)3·9H2O solution. Mix thoroughly. Preparation of Medium: Aseptically distribute cooled sterile agar phase into sterile blood culture bottles in 100.0mL volumes. Allow bottles to cool in a slanted position. Aseptically add 50.0mL of sterile broth phase to each blood culture bottle.
Use: For the isolation and cultivation of Legionella pneumophila and other Legionella species from blood samples.
BCYE Selective Agar with CCVC (Buffered Charcoal Yeast Extract Selective Agar with Cephalothin, Colistin, Vancomycin, and Cycloheximide) Composition per 1014.0mL: Agar ..................................................................15.0g Yeast extract......................................................10.0g ACES buffer (2-[(2-Amino-2-oxoethyl)amino]-ethane sulfonic acid) ......................10.0g Charcoal, activated..............................................2.0g α-Ketoglutarate...................................................1.0g Fe4(P2O7)3·9H2O...............................................0.25g Antibiotic solution ........................................ 10.0mL L-Cysteine·HCl·H2O solution.......................... 4.0mL pH 6.9 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. L-Cysteine·HCl·H2O
Solution: Composition per 10.0mL: L-Cysteine·HCl·H2O............................................1.0g
Preparation of L-Cysteine·HCl·H2O Solution: Add L-cysteine·HCl·H2O to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Antibiotic Solution: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except L-cysteine and antibiotic solutions, to distilled/ deionized water and bring volume to 1.0L. Mix thoroughly. Adjust medium to pH 6.9 with 1N KOH. Heat gently and bring to boil for 1 min. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Add 4.0mL of L-cysteine·HCl·H2O solution and 10.0mL of sterile antibiotic solution. Mix thoroughly. Pour into sterile Petri dishes with constant agitation to keep charcoal in suspension.
Use: For the isolation, cultivation, and maintenance of Legionella pneumophila and other Legionella species from a variety of specimens.
BCYE Selective Agar with GPVA (Buffered Charcoal Yeast Extract Selective Agar with Glycine, Polymyxin B, Vancomycin, and Anisomycin) Composition per 1014.0mL: Agar ..................................................................15.0g Yeast extract......................................................10.0g ACES buffer (2-[(2-Amino-2-oxoethyl)amino]-ethane sulfonic acid) ......................10.0g Charcoal, activated .............................................2.0g α-Ketoglutarate...................................................1.0g Fe4(P2O7)3·9H2O...............................................0.25g Antibiotic solution ........................................ 10.0mL L-Cysteine·HCl·H2O solution ......................... 4.0mL pH 6.9 ± 0.2 at 25°C L-Cysteine·HCl·H2O
Solution: Composition per 10.0mL: L-Cysteine·HCl·H2O............................................1.0g
Preparation of L-Cysteine·HCl·H2O Solution: Add L-cysteine·HCl·H2O to distilled/deionized
water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Antibiotic Solution: Composition per 10.0mL: Glycine................................................................3.0g Anisomycin.......................................................0.08g Vancomycin .....................................................5.0mg Polymyxin B .............................................. 100,000U
Preparation of Antibiotic Solution: Add com-
Antibiotic Solution: Composition per 10.0mL:
ponents to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Cycloheximide ...............................................80.0mg Colistin...........................................................16.0mg Cephalothin......................................................4.0mg Vancomycin .....................................................0.5mg
Preparation of Medium: Add components, except L-cysteine·HCl·H2O solution and antibiotic solution, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust medium to pH 6.9
BCYE Selective Agar with PAC with 1N KOH. Heat gently and bring to boil for 1 min. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Add 4.0mL of L-cysteine·HCl·H2O solution and 10.0mL of sterile antibiotic solution. Mix thoroughly. Pour into sterile Petri dishes with constant agitation to keep charcoal in suspension.
Use: For the isolation, cultivation, and maintenance of Legionella pneumophila and other Legionella species.
BCYE Selective Agar with GVPC (Buffered Charcoal Yeast Extract Selective Agar with Glycine, Vancomycin, Polymyxin B, and Cycloheximide) Composition per 1014.0mL: Agar ..................................................................15.0g Yeast extract......................................................10.0g ACES buffer (2-[(2-Amino-2-oxoethyl)amino]-ethane sulfonic acid) ......................10.0g Charcoal, activated..............................................2.0g α-Ketoglutarate...................................................1.0g Fe4(P2O7)3·9H2O...............................................0.25g Antibiotic solution ........................................ 10.0mL L-Cysteine·HCl·H2O solution ......................... 4.0mL pH 6.9 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath. L-Cysteine·HCl·H2O
Solution: Composition per 10.0mL: L-Cysteine·HCl·H2O............................................1.0g
Preparation of L-Cysteine·HCl·H2O Solution: Add L-cysteine·HCl·H2O to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Antibiotic Solution: Composition per 10.0mL: Glycine................................................................3.0g Cycloheximide ..................................................0.08g Vancomycin .....................................................1.0mg Polymyxin B ................................................79,200U
53
otic solution. Mix thoroughly. Pour into sterile Petri dishes with constant agitation to keep charcoal in suspension.
Use: For the isolation, cultivation, and maintenance of Legionella pneumophila and other Legionella species.
BCYE Selective Agar with PAC (Buffered Charcoal Yeast Extract Selective Agar with Polymyxin B, Anisomycin, and Cefamandole) Composition per 1014.0mL: Agar ..................................................................15.0g Yeast extract......................................................10.0g ACES buffer (2-[(2-Amino-2-oxoethyl)amino]-ethane sulfonic acid) ......................10.0g Charcoal, activated .............................................2.0g α-Ketoglutarate...................................................1.0g Fe4(P2O7)3·9H2O...............................................0.25g Antibiotic solution ........................................ 10.0mL L-Cysteine·HCl·H2O solution ......................... 4.0mL pH 6.9 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. L-Cysteine·HCl·H2O
Solution: Composition per 10.0mL: L-Cysteine·HCl·H2O............................................1.0g
Preparation of L-Cysteine·HCl·H2O Solution: Add L-cysteine·HCl·H2O to distilled/deionized
water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Antibiotic Solution: Composition per 10.0mL: Polymyxin B .......................................... 80,000 units Anisomycin....................................................80.0mg Cefamandole ....................................................2.0mg
Preparation of Antibiotic Solution: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Antibiotic Solution: Add com-
Preparation of Medium: Add components, ex-
ponents to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
cept L-cysteine solution and antibiotic solution, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust medium to pH 6.9 with 1N KOH. Heat gently and bring to boil for 1 min. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Add 4.0mL of L-cysteine solution and 10.0mL of sterile antibiotic solution. Mix thoroughly. Pour into sterile Petri dishes with constant agitation.
Preparation of Medium: Add components, except L-cysteine·HCl·H2O solution and antibiotic solution, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust medium to pH 6.9 with 1N KOH. Heat gently and bring to boil for 1 min. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Add 4.0mL of L-cysteine·HCl·H2O solution and 10.0mL of sterile antibi-
Use: For the isolation, cultivation, and maintenance of Legionella pneumophila and other Legionella species.
54
BCYE Selective Agar with PAV
BCYE Selective Agar with PAV (Buffered Charcoal Yeast Extract Selective Agar with Polymyxin B, Anisomicin, and Vancomycin) (Wadowsky–Yee Medium) Composition per 1014.0mL: Agar ..................................................................15.0g Yeast extract......................................................10.0g ACES buffer (2-[(2-Amino-2-oxoethyl)amino]-ethane sulfonic acid) ......................10.0g Charcoal, activated..............................................2.0g α-Ketoglutarate...................................................1.0g Fe4(P2O7)3·9H2O...............................................0.25g Antibiotic solution ........................................ 10.0mL L-Cysteine·HCl·H2O solution ......................... 4.0mL pH 6.9 ± 0.2 at 25°C
Yeast extract......................................................10.0g ACES buffer (2-[(2-Amino-2-oxoethyl)amino]-ethane sulfonic acid) ......................10.0g Charcoal, activated .............................................2.0g α-Ketoglutarate...................................................1.0g Bovine serum albumin solution .................... 10.0mL L-Cysteine·HCl·H2O solution ....................... 10.0mL Fe4(P2O7)3·9H2O solution............................. 10.0mL pH 6.9 ± 0.2 at 25°C
Bovine Serum Albumin Solution: Composition per 10.0mL: Bovine serum albumin........................................0.1g
Preparation of Bovine Serum Albumin Solution: Add bovine serum albumin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
L-Cysteine·HCl·H2O
L-Cysteine·HCl·H2O
L-Cysteine·HCl·H2O............................................0.4g
L-Cysteine·HCl·H2O............................................1.0g
Preparation of L-Cysteine·HCl·H2O Solution: Add L-cysteine·HCl·H2O to distilled/deionized
Solution: Composition per 10.0mL: Preparation of L-Cysteine·HCl·H2O Solution: Add L-cysteine·HCl·H2O to distilled/deionized
Solution: Composition per 10.0mL:
water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Fe4(P2O7)3·9H2O Solution: Composition per 10.0mL:
Antibiotic Solution: Composition per 10.0mL:
Fe4(P2O7)3·9H2O...............................................0.25g
Polymyxin B ..........................................40,000 units Anisomycin....................................................80.0mg Vancomycin .....................................................0.5mg
Add Fe4(P2O7)3·9H2O to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Antibiotic Solution: Add com-
Preparation of Medium: Add components—ex-
ponents to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except L-cysteine and antibiotic solution, to distilled/ deionized water and bring volume to 1.0L. Mix thoroughly. Adjust medium to pH 6.9 with 1N KOH. Heat gently and bring to boil for 1 min. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Add 4.0mL of L-cysteine·HCl·H2O solution and 10.0mL of sterile antibiotic solution. Mix thoroughly. Pour into sterile Petri dishes with constant agitation to keep charcoal in suspension.
Use: For the isolation, cultivation, and maintenance of
Preparation of Fe4(P2O7)3·9H2O Solution:
cept L-cysteine·HCl·H2O solution, Fe4(P2O7)3·9H2O solution, and bovine serum albumin solution—to distilled/deionized water and bring volume to 970.0mL. Mix thoroughly. Adjust medium to pH 6.9 with 1N KOH. Heat gently and bring to boil for 1 min. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Aseptically add the L-cysteine·HCl·H2O solution, Fe4(P2O7)3·9H2O solution, and 10.0mL of sterile bovine serum albumin solution. Mix thoroughly. Pour into sterile Petri dishes with constant agitation to keep charcoal in suspension.
Use: For the isolation, cultivation, and maintenance of Legionella pneumophila and other Legionella species.
Legionella pneumophila and other Legionella species.
BCYEα with Alb (Buffered Charcoal Yeast Extract Agar with Albumin) Composition per liter: Agar ..................................................................15.0g
BCYEα without L-Cysteine (Buffered Charcoal Yeast Extract Agar without L-Cysteine) Composition per liter: Agar ..................................................................15.0g Yeast extract......................................................10.0g
Beef Infusion Agar ACES buffer (2-[(2-Amino-2-oxoethyl)amino]-ethane sulfonic acid) ......................10.0g Charcoal, activated..............................................2.0g α-Ketoglutarate...................................................1.0g Fe4(P2O7)3·9H2O solution............................. 10.0mL pH 6.9 ± 0.2 at 25°C
Fe4(P2O7)3·9H2O Solution: Composition per 10.0mL:
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Mix thoroughly. Heat gently and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of a wide variety of microorganisms, including Alcaligenes species and Pseudomonas aeruginosa.
Fe4(P2O7)3·9H2O...............................................0.25g
Beef Extract Broth
Preparation of Fe4(P2O7)3·9H2O Solution:
Composition per liter:
Add Fe4(P2O7)3·9H2O to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Peptone ...............................................................5.0g Beef extract.........................................................3.0g pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components, ex-
Preparation of Medium: Add components to
cept Fe4(P2O7)3·9H2O solution, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Adjust medium to pH 6.9 with 1N KOH. Heat gently and bring to boil for 1 min. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Aseptically add 10.0mL of sterile Fe4(P2O7)3·9H2O solution. Mix thoroughly. Pour into sterile Petri dishes with constant agitation to keep charcoal in suspension.
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Heat gently and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the isolation, cultivation, and maintenance of Legionella pneumophila and other Legionella species.
Beef Extract Agar Composition per liter: Agar ..................................................................15.0g Peptone................................................................5.0g Beef extract .........................................................3.0g pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Heat gently and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of a wide variety of microorganisms.
Beef Extract Agar (ATCC Medium 225) Composition per liter: Agar ..................................................................25.0g Beef extract .......................................................10.0g Peptone..............................................................10.0g NaCl ....................................................................5.0g pH 7.2 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L.
Use: For the cultivation and maintenance of a wide variety of microorganisms.
Beef Extract Peptone Serum Medium Composition per liter: Agar ..................................................................25.0g Beef extract.......................................................10.0g Peptone .............................................................10.0g NaCl....................................................................1.0g Bovine serum ................................................ 50.0mL pH 8.5 ± 0.2 at 25°C
Preparation of Medium: Add components, except bovine serum, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Adjust pH to 8.5. Heat gently and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Aseptically add 50.0mL of sterile bovine serum. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of Serratia marcescens.
Beef Infusion Agar Composition per liter: Ground defatted beef ......................................453.6g Agar ..................................................................20.0g Peptone .............................................................10.0g NaCl....................................................................5.0g pH 7.6 ± 0.2 at 25°C
Preparation of Medium: Add ground beef to 1.0L of distilled/deionized water. Let stand overnight at 4°C. Gently heat and bring to 80°–90°C for 60 min. Let stand for 2h. Filter through muslin. To filtrate, add peptone and salt. Mix thoroughly. Adjust pH to 7.6 with 4% NaOH. Filter through Whatman #1 filter paper. Bring
56
Beef Infusion Broth
volume of filtrate to 1.0L. Add agar. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation of a variety of microorganisms.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.3. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of Actino-
Beef Infusion Broth Composition per liter: Ground beef, defatted .....................................453.6g Peptone..............................................................10.0g NaCl ....................................................................5.0g pH 7.6 ± 0.2 at 25°C
Preparation of Medium: Add ground beef to 1.0L of distilled/deionized water. Let stand overnight at 4°C. Gently heat and bring to 80°–90°C for 60 min. Let stand for 2h. Filter through muslin. To filtrate add peptone and salt. Mix thoroughly. Adjust pH to 7.6 with 4% NaOH. Filter through Whatman #1 filter paper. Bring volume of filtrate to 1.0L. Add agar. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of a variety of microorganisms.
Beef Liver Medium for Anaerobes
madura spp., Nocardia spp., and Streptomyces species.
Bennett’s Agar with Maltose Composition per liter: Agar ..................................................................15.0g Maltose, technical .............................................10.0g N-Z amine, type A ..............................................2.0g Beef extract.........................................................1.0g Yeast extract........................................................1.0g pH 7.3 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.3. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of Streptomyces species.
Composition per liter: Beef liver, minced ...........................................500.0g Peptone..............................................................10.0g K2HPO4 ...............................................................1.0g pH 8.0 ± 0.2 at 25°C
Preparation of Medium: Add beef liver to 1.0L of tap water. Soak for 12–24h at 4°C. Skim fat off top. Autoclave for 10 min at 15 psi pressure–121°C. Filter through cheesecloth. Save meat. To filtrate, add peptone and K2HPO4. Adjust pH to 8.0. Filter through paper. Add tap water and bring volume to 1.0L. Add a small amount of CaCO3 to a flask or test tube. Add 0.5 inch of reserved liver. Cover meat with 2 inches of broth. Cap tubes and autoclave for 15 min at 15 psi pressure– 121°C.
Bennett’s Modified Agar Medium Composition per liter: Meer agar (washed agar) ..................................20.0g Dextrin ..............................................................10.0g Pancreatic digest of casein..................................2.0g Yeast extract........................................................1.0g Beef extract.........................................................1.0g CoCl2·6H2O ......................................................0.01g pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Add components to
Use: For the cultivation and maintenance of a vari-
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Heat gently to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
ety of Clostridium species.
Use: For the cultivation and maintenance of Streptomyces species.
Bennett’s Agar Composition per liter: Agar ..................................................................15.0g Glucose .............................................................10.0g N-Z amine, type A ..............................................2.0g Beef extract .........................................................1.0g Yeast extract........................................................1.0g pH 7.3 ± 0.2 at 25°C
BG Sulfa Agar (Brilliant Green Sulfapyridine Agar) Composition per liter: Agar ..................................................................20.0g Proteose peptone no. 3......................................10.0g Lactose..............................................................10.0g Sucrose..............................................................10.0g
BHI with Glycerol and Reducing Agents NaCl ....................................................................5.0g Yeast extract........................................................3.0g Sodium sulfapyridine..........................................1.0g Brilliant Green ................................................0.125g pH 6.9 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Heat gently to boiling. Distribute into tubes or flasks. Autoclave for no longer than 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes if desired.
Use: For the selective isolation of Salmonella species other than Salmonella typhi. Salmonella appear as red, pink, or white colonies surrounded by zones of bright red.
BHI with Glucose (DSMZ Medium 215b) Composition per liter: Pancreatic digest of gelatin ...............................14.5g Glucose ...............................................................8.0g Brain heart, solids from infusion ........................6.0g Peptic digest of animal tissue..............................6.0g NaCl ....................................................................5.0g Na2HPO4 .............................................................2.5g pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of Corynebacterium spp., Streptomyces flocculus, Mycobacterium spp., Nocardia spp., Rhodococcus spp., Dermatophilus congolensis, and Gordonia amicalis.
BHI Glucose Medium Composition per liter: Agar ..................................................................12.0g Pancreatic digest of gelatin ...............................7.25g Glucose ...............................................................6.5g Brain heart, solids from infusion ........................3.0g Peptic digest of animal tissue..............................3.0g NaCl ....................................................................2.5g Na2HPO4 ...........................................................1.25g pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min
57
at 15 psi–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of Actinomadura spp., Dermatophilus spp., Mycobacterium species, Nocardia asteroides, and Streptococcus pyogenes.
BHI with Glycerol and Reducing Agents (DSMZ Medium 215c) Composition per liter: Pancreatic digest of gelatin...............................14.5g Brain heart, solids from infusion ........................6.0g Peptic digest of animal tissue .............................6.0g NaCl....................................................................5.0g Glucose ...............................................................3.0g Na2HPO4 .............................................................2.5g Glycerol solution .......................................... 10.0mL L-Cysteine·HCl–Na2S solution ..................... 10.0mL pH 7.4 ± 0.2 at 25°C
Glycerol Solution: Composition per 100.0mL: Glycerol ............................................................87.0g
Preparation of Glycerol Solution: Add glycerol to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. L-Cysteine·HCl–Na2S
Solution: Composition per 100.0mL: L-Cysteine·HCl....................................................2.5g
Na2S·9H2O .........................................................2.5g
Preparation of L-Cysteine·HCl–Na2S Solution: Add L-cysteine·HCl to distilled/deionized water and bring volume to 80.0mL. Mix thoroughly. Adjust pH to 11 with NaOH. Add Na2S·9H2O. Mix thoroughly. Bring volume to 100.0mL with distilled/ deionized water. Gently heat and bring to boiling under 100% N2. Cool to 25°C under 100% N2. Autoclave for 15 min at 15 psi pressure–121°C.
Preparation of Medium: Add components, except L-cysteine·HCl–Na2S solution, to distilled/ deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling under 100% N2. Cool to 25°C under 100% N2. Autoclave for 15 min at 15 psi pressure–121°C. Aseptically and anaerobically under 100% N2 add 10.0mL of cysteine·HCl–Na2S solution. Mix thoroughly. Aseptically under 100% N2 distribute to tubes. Alternately distribute 10.0mL amounts of the medium without cysteine·HCl–Na2S solution to tubes prior to autoclaving. Autoclave for 15 min at 15 psi pressure– 121°C. Aseptically and anaerobically add 1.0mL of cysteine·HCl–Na2S solution to each tube.
Use: For the cultivation of Clostridium sp.
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BHI Medium
BHI Medium (DSMZ Medium 215) Composition per liter: Pancreatic digest of gelatin ...............................14.5g Brain heart, solids from infusion ........................6.0g Peptic digest of animal tissue..............................6.0g NaCl ....................................................................5.0g Na2HPO4 .............................................................2.5g pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of Yersinia spp., Oligella urethralis=Moraxella urethralis, Moraxella (Branhamella) catarrhalis, Campylobacter sputorum, and Corynebacterium spp.
BHI/1 Medium
BHI/3 Medium Composition per liter: Pancreatic digest of gelatin...............................14.5g Casein hydrolysate............................................10.0g Brain heart, solids from infusion ........................6.0g Peptic digest of animal tissue .............................6.0g Starch ..................................................................5.0g NaCl....................................................................5.0g Glucose ...............................................................3.0g Na2HPO4 .............................................................2.5g pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi–121°C.
Use: For the cultivation and maintenance of Actinomyces species.
Bifidobacterium Medium
Composition per liter:
Composition per liter:
Pancreatic digest of gelatin ...............................14.5g Casein hydrolysate............................................10.0g Glucose ...............................................................8.0g Brain heart, solids from infusion ........................6.0g Peptic digest of animal tissue..............................6.0g NaCl ....................................................................5.0g Na2HPO4 .............................................................2.5g pH 7.4 ± 0.2 at 25°C
Glucose .............................................................20.0g Pancreatic digest of casein................................20.0g Yeast extract......................................................10.0g Peptone .............................................................10.0g Tomato juice ............................................... 333.0mL Tween™ 80..................................................... 2.0mL pH 6.8 ± 0.2 at 25°C
Preparation of Medium: Add components to
tomato juice with 666.0mL of distilled/deionized water. Bring to boiling. Filter through paper. Add remaining components to filtrate. Mix thoroughly. Bring volume to 1.0L with distilled/deionized water. Distribute into tubes or flasks. Autoclave for 30 min at 15 psi pressure–110°C.
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi–121°C.
Use: For the cultivation and maintenance of Actinomyces israelii and Propionibacterium propionicus.
Preparation of Medium: Combine 333.0mL of
Use: For the cultivation of Bifidobacterium infantis.
BHI/2 Medium Composition per liter: Pancreatic digest of gelatin ...............................14.5g Casein hydrolysate............................................10.0g Glucose ...............................................................8.0g Brain heart, solids from infusion ........................6.0g Peptic digest of animal tissue..............................6.0g NaCl ....................................................................5.0g Yeast extract........................................................5.0g Na2HPO4 .............................................................2.5g pH 7.4 ± 0.2 at 25°C
Bifidobacterium Medium Composition per liter: Special peptone.................................................23.0g Agar ..................................................................15.0g NaCl....................................................................5.0g Glucose ...............................................................5.0g Starch, soluble.....................................................1.0g L-Cysteine·HCl ...................................................0.3g
Preparation of Medium: Add components to
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of Actino-
Use: For the cultivation and maintenance of numer-
myces spp.
ous Bifidobacterium species.
Preparation of Medium: Add components to
Bile Esculin Agar
BiGGY Agar (Bismuth Sulfite Glucose Glycerin Yeast Extract Agar) (Nickerson Medium) Composition per liter: Agar ..................................................................16.0g Glucose .............................................................10.0g Glycine..............................................................10.0g Bismuth ammonium citrate.................................5.0g Na2SO3 ................................................................3.0g Yeast extract........................................................1.0g pH 6.8 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath and BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly and heat with frequent agitation until boiling. Distribute into tubes or flasks. Do not autoclave. Cool to approximately 45°–50°C. If desired, add 2mg/L of neomycin sulfate. Swirl to disperse the insoluble material and pour into sterile Petri dishes.
Use: For the detection, isolation, and presumptive identification of Candida species. Addition of neomycin helps inhibit bacterial species. Candida albicans appears as brown to black colonies with no pigment diffusion and no sheen. Candida tropicalis appears as dark brown colonies with black centers, black pigment diffusion, and a sheen. Candida krusei appears as shiny, wrinkled, brown to black colonies with yellow pigment diffusion. Candida pseudotropicalis appears as flat, shiny red to brown colonies with no pigment diffusion. Candida parakrusei appears as flat, shiny, wrinkled, dark reddish-brown colonies with light reddish-brown peripheries and a yellow fringe. Candida stellatoidea appears as flat dark brown colonies with a light fringe.
Bile Esculin Agar Composition per liter: Oxgall................................................................20.0g Agar ..................................................................15.0g Pancreatic digest of gelatin .................................5.0g Beef extract .........................................................3.0g Esculin ................................................................1.0g Ferric citrate........................................................0.5g Horse serum .................................................. 50.0mL pH 6.8 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath and BD Diagnostic Systems.
59
Preparation of Medium: Add components, except horse serum, to distilled/deionized water and bring volume to 950.0L. Mix thoroughly and heat with frequent agitation until boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 50.0mL of filter sterilized horse serum. Distribute into sterile Petri dishes or test tubes. Cool tubes in a slanted position.
Use: For differentiation between group D streptococci and nongroup D streptococci. To differentiate members of the Enterobacteriaceae, particularly Klebsiella, Enterobacter, and Serratia, from other enteric bacteria. To differentiate Listeria monocytogenes. Bile tolerance and esculin hydrolysis (seen as a dark brown to black complex) are presumptive for enterococci (group D streptococci).
Bile Esculin Agar Composition per liter: Esculin ................................................................1.0g Bile esculin agar base ........................................ 1.0L pH 6.6 ± 0.2 at 25°C
Bile Esculin Agar Base: Composition per liter: Oxgall ...............................................................40.0g Agar ..................................................................15.0g Peptone ...............................................................5.0g Beef extract.........................................................3.0g Ferric citrate........................................................0.5g
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Bile Esculin Agar Base: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly.
Preparation of Medium: Add desired amount of esculin—typically 1.0g—to bile esculin agar base. Mix thoroughly and heat with frequent agitation until boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C. Distribute into sterile Petri dishes or test tubes. Cool tubes in a slanted position.
Use: For the isolation and presumptive identification of group D streptococci.
Bile Esculin Agar Composition per liter: Oxgall ...............................................................40.0g Agar ..................................................................15.0g Pancreatic digest of gelatin.................................5.0g Beef extract.........................................................3.0g Esculin ................................................................1.0g Ferric citrate........................................................0.5g pH 6.6 ± 0.2 at 25°C
60
Bile Esculin Agar with Kanamycin
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly and heat with frequent agitation until boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Distribute into sterile Petri dishes or test tubes. Cool tubes in a slanted position.
Use: For differentiation between group D streptococci and nongroup D streptococci. To differentiate members of the Enterobacteriaceae, particularly Klebsiella, Enterobacter, and Serratia, from other enteric bacteria. To differentiate Listeria monocytogenes. Bile tolerance and esculin hydrolysis (seen as a dark brown to black complex) are presumptive for enterococci (group D streptococci).
Bile Esculin Azide Agar Composition per liter: Pancreatic digest of casein................................17.0g Agar ..................................................................15.0g Oxgall ...............................................................10.0g NaCl....................................................................5.0g Yeast extract........................................................5.0g Proteose peptone no. 3........................................3.0g Esculin ................................................................1.0g Ferric ammonium citrate.....................................0.5g NaN3 .................................................................0.15g pH 7.1 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Bile Esculin Agar with Kanamycin
Caution: Sodium azide is toxic. Azides also react
Composition per liter:
with metals and disposal must be highly diluted.
Oxgall................................................................20.0g Agar ..................................................................15.0g Beef extract .........................................................3.0g Esculin ................................................................1.0g Ferric citrate........................................................0.5g Hemin.............................................................10.0mg Vitamin K1 .....................................................10.0mg Horse serum .................................................. 50.0mL Kanamycin solution ...................................... 10.0mL pH 7.1 ± 0.2 at 25°C
Preparation: Add components to distilled/deion-
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Kanamycin Solution: Composition per 10.0mL: Kanamycin ..........................................................1.0g
Preparation of Kanamycin Solution: Add kanamycin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly and heat with frequent agitation until boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C. Aseptically add 50.0mL of 5% filter-sterilized horse serum and 10.0mL of sterile kanamycin solution. Distribute into test tubes or flasks. Cool tubes in a slanted position.
Use: For the selective isolation and/or presumptive identification of bacteria of the Bacteroides fragilis group from specimens containing mixed flora. Examine colonies with a long-wavelength UV light. Pigmented colonies of the Bacteroides group will fluoresce red-orange. Growth on this medium with blackening of the medium is presumptive for Bacteroides fragilis.
ized water and bring volume to 1.0L. Mix thoroughly and heat with frequent agitation until boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Pour into sterile Petri dishes or leave in tubes. Cool tubes in a slanted position.
Use: For the isolation and presumptive identification of group D streptococci.
Bile Oxalate Sorbose Broth (BOS Broth) Composition per liter: Na2HPO4 ...........................................................9.14g Sodium oxalate ...................................................5.0g Bile salts..............................................................2.0g NaCl....................................................................1.0g CaCl2·2H2O ......................................................0.01g MgSO4·7H2O ....................................................0.01g Asparagine solution .................................... 100.0mL Methionine solution .................................... 100.0mL Sorbose solution.......................................... 100.0mL Yeast extract solution.................................... 10.0mL Sodium pyruvate solution ............................. 10.0mL Metanil Yellow solution................................ 10.0mL Sodium nitrofurantoin solution..................... 10.0mL Irgasan® solution............................................ 1.0mL pH 7.6 ± 0.2 at 25°C
Asparagine Solution: Composition per 100.0mL: Asparagine ..........................................................1.0g
Preparation of Asparagine Solution: Add asparagine to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Bile Salts Gelatin Agar Methionine Solution: Composition per 100.0mL: Methionine ..........................................................1.0g
Preparation of Methionine Solution: Add methionine to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Sorbose Solution: Composition per 100.0mL: Sorbose..............................................................10.0g
Preparation of Sorbose Solution: Add sorbose to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize. Yeast Extract Solution: Composition per 10.0mL: Yeast extract....................................................0.025g
Preparation of Yeast Extract Solution: Add yeast extract to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Sodium Pyruvate Solution: Composition per 10.0mL: Sodium pyruvate ...............................................0.05g
Preparation of Sodium Pyruvate Solution: Add sodium pyruvate to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Metanil Yellow Solution: Composition per 10.0mL: Metanil Yellow................................................0.025g
Preparation of Metanil Yellow Solution: Add Metanil Yellow to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Sodium Nitrofurantoin Solution: Composition per 10.0mL:
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Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 100.0mL of sterile asparagine solution, 100.0mL of sterile methionine solution, 100.0mL of sterile sorbose solution, 10.0mL of sterile yeast extract solution, 10.0mL of sterile sodium pyruvate solution, 10.0mL of sterile Metanil Yellow solution, 10.0mL of sterile sodium nitrofurantoin solution, and 1.0mL of sterile Irgasan solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation and cultivation of Yersinia enterocolitica.
Bile Salts Brilliant Green Starch Agar (BBGS Agar) Composition per liter: Agar ..................................................................15.0g Soluble starch....................................................10.0g Proteose peptone...............................................10.0g Beef extract.........................................................5.0g Bile salts..............................................................5.0g Brilliant Green (0.05% solution) .................... 1.0mL pH 7.2 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the isolation and cultivation of Aeromonas hydrophila.
Bile Salts Gelatin Agar
Sodium nitrofurantoin.......................................0.01g
Composition per 100.0mL:
Preparation of Sodium Nitrofurantoin Solution: Add sodium nitrofurantoin to distilled/deion-
Gelatin.................................................................3.0g Agar ....................................................................1.5g Pancreatic digest of casein..................................1.0g NaCl....................................................................1.0g Sodium taurocholate ...........................................0.5g Na2CO3 ...............................................................0.1g Water........................................................... 100.0mL pH 8.5 ± 0.2 at 25°C
ized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Irgasan Solution: Composition per 10.0mL: Irgasan...............................................................0.04g Ethanol (95% solution) ................................. 10.0mL
Preparation of Irgasan Solution: Add Irgasan to 10.0mL of ethanol. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except asparagine solution, methionine solution, sorbose solution, yeast extract solution, sodium pyruvate solution, Metanil Yellow solution, sodium nitrofurantoin solution, and Irgasan solution, to distilled/deionized water and bring volume to 659.0mL. Mix thoroughly.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation of Vibrio cholerae.
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BIN Medium
BIN Medium Composition per liter: Beef heart, infusion from ................................250.0g Calf brains, infusion from...............................200.0g Agar ..................................................................15.0g Proteose peptone ...............................................10.0g NaCl ....................................................................5.0g Na2HPO4 .............................................................2.5g Glucose ...............................................................2.0g Irgasan solution............................................... 4.0mL Crystal Violet solution .................................... 1.0mL Sodium cholate solution.................................. 1.0mL Sodium deoxycholate solution........................ 1.0mL Nystatin solution ............................................. 1.0mL pH 7.4 ± 0.2 at 25°C
Sodium Cholate Solution: Composition per 100.0mL: Sodium cholate ...................................................5.0g
Preparation of Sodium Cholate Solution: Add sodium cholate to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C.
Sodium Deoxycholate Solution: Composition per 100.0mL: Sodium cholate ...................................................5.0g
Preparation of Sodium Deoxycholate Solution: Add sodium deoxycholate to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool 25°C.
Irgasam Solution: Composition per 50.0mL: Irgasan DP300................................................10.0mg Ethanol, 90%................................................. 50.0mL
Preparation of Irgasam Solution: Add irgasam to 90% ethanol and bring volume to 50.0mL. Mix thoroughly.
Crystal Violet Solution: Composition per 10.0mL: Crystal Violet .................................................10.0mg
Preparation of Sodium Cholate Solution: Add Crystal Violet to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C.
Nystatin Solution: Composition per 10.0mL: Nystatin ..............................................................2.5g
Preparation of Nystatin Solution: Add novobiocin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except irgasan solution, Crystal Violet solution, sodium cholate solution, sodium deoxycholate solution, and nystatin solution, to distilled/deionized water and bring volume to 992.0mL. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 85°C. Aseptially add 4.0mL irgasam solution. Mix thoroughly to volatilize the ethanol. Cool to 50°C. Aseptially add 1.0mL each of Crystal Violet solution, sodium cholate solution, sodium deoxycholate solution, and nystatin solution. Mix thouroughly. Pour into sterile Petri dishes.
Use: For the efficient detection of Yersinia pestis from clinical and other specimens. The formulation of this medium is based on brain heart infusion agar, to which the selective agents irgasan, cholate salts, crystal violet, and nystatin are introduced to enhance efficiency of recovery of Y. pestis.
Biosynth Chromogenic Medium for Listeria monocytogenes (BCM for Listeria monocytogenes) Composition per liter: Proprietary
Source: This medium is available from Biosynth International, Inc.
Use: To differentiate Listeria monocytogenes and L. ivanovii from other Listeria spp. Supplements render the medium selective. Differential activity for all Listeria species is based upon a chromogenic substrate included in the medium. This is a complete test system with a fluorogenic selective enrichment broth and a chromogenic plating medium both detecting the virulence factor Phosphatidylinositol specific Phospholipase C (PI-PLC). The medium contains a substrate for phosphotidylinositol-specific phospholipase C (PlcA) enzymes. The selective enrichment broth is fluorogenic. The plating medium for rapid detection and enumeration of pathogenic Listeria combines cleavage of the chromogenic PI-PLC substrate with the additional production of a white precipitate surrounding the target colonies.
Biphasic Medium for Neisseria Composition per liter: Glucose starch agar............................................ 1.0L Glucose starch broth .......................................... 1.0L pH 7.3 ± 0.2 at 25°C
Bismuth Sulfite Agar Wilson and Blair Glucose Starch Agar: Composition per liter: Agar ..................................................................20.0g Gelatin...............................................................20.0g Proteose peptone no. 3 ......................................15.0g Soluble starch....................................................10.0g NaCl ....................................................................5.0g Na2HPO4 .............................................................3.0g Glucose ...............................................................2.0g
Preparation of Glucose Starch Agar: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C.
Glucose Starch Broth: Composition per liter: Gelatin...............................................................20.0g Proteose peptone no. 3 ......................................15.0g Soluble starch....................................................10.0g NaCl ....................................................................5.0g Glucose ...............................................................2.0g Na2HPO4 .............................................................3.0g
Preparation of Glucose Starch Broth: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C. Preparation of Medium: Aseptically distibute glucose starch agar into flasks in 100–125mL volumes. Allow agar to solidify. Overlay agar with 25.0mL of sterile glucose starch broth. Use: For selective isolation and cultivation of Neisseria species.
Bird Seed Agar (Guizotia abyssinica Creatinine Agar) (Niger Seed Agar)/(Staib Agar) Composition per liter: Agar ..................................................................15.0g Glucose .............................................................15.0g Creatinine............................................................5.0g KH2PO4 ...............................................................3.0g Biphenyl..............................................................1.0g Chloramphenicol.................................................0.5g Guizotia abyssinica seed (niger seed) extract ............................. 1000.0mL pH 6.7 ± 0.2 at 25°C
Preparation of Medium: Prepare seed extract by grinding 50.0g of Guizotia abyssinica seed in 1.0L of distilled/deionized water. Boil for 30 min. Filter through cheesecloth and filter paper. Add remaining components to seed filtrate. Mix thoroughly and heat
63
with frequent agitation until boiling. Distribute into flasks or tubes. Autoclave for 25 min at 15 psi pressure–110°C.
Use: For the selective isolation and differentiation of Cryptococcus neoformans from other Cryptococcus species and other yeasts.
Bismuth Sulfite Agar Composition per liter: Agar ..................................................................20.0g Bi2(SO3)3 ............................................................8.0g Pancreatic digest of casein..................................5.0g Peptic digest of animal tissue .............................5.0g Beef extract.........................................................5.0g Glucose ...............................................................5.0g Na2HPO4 .............................................................4.0g FeSO4·7H2O........................................................0.3g pH 7.5 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath and BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly and heat with frequent agitation until boiling. Boil for 1 min. Do not autoclave. Cool to 45°–50°C. Pour into sterile Petri dishes while gently shaking flask to disperse precipitate. Use plates the same day as prepared.
Use: For the selective isolation and identification of Salmonella typhi and other enteric bacilli. Salmonella typhi appears as flat, black, “rabbit-eye” colonies surrounded by a zone of black with a metallic sheen.
Bismuth Sulfite Agar Wilson and Blair Composition per liter: Agar ..................................................................20.0g Pancreatic digest of casein................................10.0g Bi2(SO3)3 ............................................................8.0g Beef extract.........................................................5.0g Glucose ...............................................................5.0g Na2HPO4 .............................................................4.0g FeSO4·7H2O........................................................0.3g Brilliant Green ................................................0.025g pH 7.7 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly and heat with frequent agitation until boiling. Boil for 1 min. Do not autoclave. Cool to 45°–50°C. Pour into sterile Petri dishes while gently shaking flask to disperse precipitate. Let plates dry for about 2h with lids partially removed. Use plates
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Bismuth Sulfite Broth
within one day of preparation; medium loses selectivity after 48h.
Use: For the selective isolation and identification of Salmonella typhi and other enteric bacilli. Salmonella typhi appears as flat, black, “rabbit-eye” colonies surrounded by a zone of black with a metallic sheen.
Bismuth Sulfite Broth (m-Bismuth Sulfite Broth) Composition per liter: Bi2(SO3)3 ...........................................................16.0g Pancreatic digest of casein................................10.0g Peptic digest of animal tissue............................10.0g Beef extract .......................................................10.0g Glucose .............................................................10.0g Na2HPO4 .............................................................8.0g FeSO4·7H2O........................................................0.6g pH 7.7 ± 0.2 at 25°C
Preparation of Medium: Add components to
Gently heat to 60°C. Maintain at 50°–60°C for 1h. Gently bring to boiling. Boil for 5 min. Adjust pH to 7.2. Filter through Whatman #2 filter paper. L-Cysteine·HCl
Solution: Composition per 10.0mL: L-Cysteine·HCl ...................................................0.5g
Preparation of L-Cysteine·HCl Solution: Dissolve 0.5g of L-cysteine·HCl in distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. Warm to 50°C.
Solution A: Composition per 100.0mL: K2HPO4.............................................................10.0g KH2PO4.............................................................10.0g
Preparation of Solution A: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C.
distilled/deionized water and bring volume to 1.0L. Mix thoroughly and heat with frequent agitation until boiling. Boil for 1 min. Do not autoclave. Cool to 45°–50°C. Mix to disperse the precipitate and aseptically distribute into sterile tubes or flasks. Use 2.0– 2.2mL of medium for each membrane filter.
Solution B: Composition per 100.0mL:
Use: For the selective isolation of Salmonella typhi and other enteric bacilli and for the detection of Salmonella by the membrane filter method.
Preparation of Solution B: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C.
BL Agar (Glucose Blood Liver Agar)
Preparation of Medium: Add components, ex-
Composition per liter: Agar ..................................................................15.0g Glucose .............................................................10.0g Proteose peptone no. 3 ......................................10.0g Pancreatic digest of casein..................................5.0g Yeast extract........................................................5.0g Meat extract ........................................................3.0g Phytone™ ...........................................................3.0g Tween 80.............................................................1.0g Soluble starch......................................................0.5g Liver extract................................................ 150.0mL Horse blood................................................... 50.0mL L-Cysteine·HCl solution................................ 10.0mL Solution A ..................................................... 10.0mL Solution B ....................................................... 5.0mL pH 7.2 ± 0.2 at 25°C
Liver Extract: Composition per 170.0mL: Liver powder.....................................................10.0g
Preparation of Liver Extract: Add 10.0g of liver powder to 170mL of distilled/deionized water.
MgSO4·7H2O ......................................................4.0g NaCl....................................................................0.2g FeSO4·7H2O........................................................0.2g MnSO4·H2O ........................................................0.2g
cept liver extract, horse blood, L-cysteine·HCl solution, solution A, and solution B, to distilled/ deionized water and bring volume to 775.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Aseptically add 150.0mL of sterile liver extract, 50.0mL of sterile horse blood, 10.0mL of sterile L-cysteine·HCl solution, 10.0 mL of sterile solution A, and 5.0mL of sterile solution B. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation and maintenance of Bacteroides species.
Blood Agar Composition per liter: Agar ..................................................................15.0g Pancreatic digest of casein................................15.0g Papaic digest of soybean meal............................5.0g NaCl....................................................................5.0g Sheep blood, defibrinated ............................. 50.0mL pH 7.6 ± 0.2 at 25°C
Blood Agar Base No. 2 Preparation of Medium: Add components, except sheep blood, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 50.0mL of sterile sheep blood. Mix thoroughly. Pour into sterile Petri dishes in 20.0mL volumes.
Use: For the cultivation of fastidious microorganisms.
Blood Agar Base Composition per liter: Agar ..................................................................15.0g Beef extract .......................................................10.0g Peptone..............................................................10.0g NaCl ....................................................................5.0g Sheep blood, defibrinated ............................. 50.0mL pH 7.3 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath.
Preparation of Medium: Add components, except sheep blood, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Heat with frequent agitation and boil for 1 min to completely dissolve. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C. Aseptically add 50.0mL of sterile, defibrinated sheep blood. Mix thoroughly and pour into sterile Petri dishes.
Use: For the isolation, cultivation, and detection of hemolytic activity of streptococci and other fastidious microorganisms.
Blood Agar Base (ATCC Medium 368) Composition per liter: Beef heart, infusion from ................................500.0g Agar ..................................................................15.0g Tryptose ............................................................10.0g NaCl ....................................................................5.0g pH 6.8 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Heat with frequent agitation and boil for 1 min to completely dissolve. Autoclave for 15 min at 15 psi pressure–121°C. Cool the basal medium to 45°–50°C. Aseptically add sterile, defibrinated blood to a final concentration of 5%. Mix thoroughly and pour into sterile Petri dishes.
Use: For the isolation, cultivation, and detection of hemolytic activity of staphylococci, streptococci, and other fastidious microorganisms.
65
Blood Agar Base (Infusion Agar) Composition per liter: Agar ..................................................................15.0g Pancreatic digest of casein................................13.0g NaCl....................................................................5.0g Yeast extract........................................................5.0g Heart muscle, solids from infusion.....................2.0g Sheep blood, defibrinated ............................. 50.0mL pH 7.3 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components, except sheep blood, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Heat with frequent agitation and boil for 1 min to completely dissolve. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C. Aseptically add 50.0mL of sterile, defibrinated sheep blood. Mix thoroughly and pour into sterile Petri dishes.
Use: For the isolation, cultivation, and detection of hemolytic activity of streptococci and other fastidious microorganisms.
Blood Agar Base (Infusion Agar) (FDA Medium M21) Composition per liter: Heart muscle, infusion from ...........................375.0g Agar ..................................................................15.0g Thiotone............................................................10.0g NaCl....................................................................5.0g pH 7.3 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 20 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation of a variety of microorganisms. For the preparation of blood agar by the addition of sterile blood.
Blood Agar Base No. 2 Composition per 1004mL: Proteose peptone...............................................15.0g Agar ..................................................................12.0g NaCl....................................................................5.0g Yeast extract........................................................5.0g Liver digest .........................................................2.5g
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Blood Agar Base with Peptone
Horse blood, defibrinated ............................. 50.0mL FBP solution ................................................... 4.0mL pH 7.4 ± 0.2 at 25°C
FBP Solution: Composition per 30.0mL: FeSO4 ................................................................0.25g NaHSO3 ............................................................0.25g Sodium pyruvate ...............................................0.25g
Preparation of FBP Solution: Add components to distilled/deionized water and bring volume to 30.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except horse blood and FBP solution, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 48°C. Aseptically add 50.0mL of sterile horse blood. Mix thoroughly. Aseptically add 4.0mL sterile FBP solution. Mix thoroughly. Pour into sterile Petri dishes in 20.0mL volumes.
Use: For the cultivation of Brucella spp. and other fastidious bacteria.
Blood Agar Base with Peptone Composition per liter: Agar ..................................................................15.0g Beef extract .......................................................10.0g Peptone..............................................................10.0g NaCl ....................................................................5.0g pH 7.3 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For use as a base to which blood can be added; for the isolation, cultivation, and detection of hemolytic activity of streptococci and other fastidious microorganisms.
Blood Agar Base, Sheep Composition per liter: Pancreatic digest of casein................................14.0g Agar ..................................................................12.5g NaCl ....................................................................5.0g Peptone................................................................4.5g Yeast extract........................................................4.5g Sheep blood, defibrinated ............................. 70.0mL ph 7.3 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath.
Preparation: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool the basal medium to 45°–50°C. Aseptically add 70.0mL of sterile, defibrinated sheep blood. Pour into sterile Petri dishes.
Use: For giving improved hemolytic reactions with sheep blood.
Blood Agar Base with Special Peptone Composition per liter: Agar ..................................................................15.0g Beef extract.......................................................10.0g Special peptone.................................................10.0g NaCl....................................................................5.0g Sheep blood, defibrinated ............................. 50.0mL pH 7.3 ± 0.2 at 25°C
Source: Special peptone (L72) is available from Oxoid Unipath.
Preparation of Medium: Add components, except sheep blood, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Heat with frequent agitation and boil for 1 min to completely dissolve. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C. Aseptically add 50.0mL of sterile, defibrinated sheep blood. Mix thoroughly and pour into sterile Petri dishes.
Use: For the isolation, cultivation, and detection of hemolytic activity of streptococci and other fastidious microorganisms.
Blood Agar, Diphasic Composition per 800.0mL: Lean beef, desiccated........................................25.0g Agar ..................................................................10.0g Neopeptone .......................................................10.0g NaCl....................................................................2.5g Locke solution ............................................ 200.0mL Rabbit blood, defibrinated .......................... 100.0mL pH 7.2–7.4 at 25°C
Locke Solution: Composition per liter: NaCl....................................................................8.0g Glucose ...............................................................2.5g KH2PO4...............................................................0.3g KCl......................................................................0.2g CaCl2·2H2O ........................................................0.2g
Preparation of Locke Solution: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add beef to 500.0mL of distilled/deionized water. Let stand for 60 min.
Blood Base Agar with Charcoal Gently heat and bring to 80°C for 5 min. Filter through Whatman #1 filter paper. To filtrate, add remaining components, except Locke solution and rabbit blood. Mix thoroughly. Adjust pH to 7.2–7.4 with NaOH. Autoclave for 20 min at 15 psi pressure– 121°C. Cool to 45°–50°C. Aseptically add sterile rabbit blood. Mix thoroughly. Aseptically distribute into sterile tubes in 5.0mL volumes. Allow tubes to cool in a slanted position. Immediately prior to inoculation, overlay agar in each tube with 2.0mL of sterile Locke solution.
Use: For the cultivation of Trypanosoma species and Leishmania species.
Blood Agar, Diphasic Base Medium Composition per 750.0mL: Beef...................................................................25.0g Agar ..................................................................10.0g Neopeptone .......................................................10.0g NaCl ....................................................................2.5g pH 7.2–7.4 at 25°C
Preparation of Medium: Trim beef to remove fat. Add 25.0g of lean beef to 250.0mL of distilled/ deionized water. Gently heat and bring to boiling. Boil for 2–3 min. Filter through Whatman #2 filter paper. Add agar, neopeptone, and NaCl to filtrate. Bring volume to 750.0mL with distilled/deionized water. Mix thoroughly. Adjust pH to 7.2–7.4. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or distribute into sterile tubes. Use: For the cultivation of Trypanosoma species.
Blood Agar with Low pH Composition per liter: Beef heart, solids from infusion......................500.0g Agar ..................................................................15.0g Tryptose ............................................................10.0g NaCl ....................................................................5.0g Sheep blood, defibrinated ............................. 50.0mL pH 6. 8 ± 0.2 at 25°C
67
Use: For the isolation and growth of a wide variety of microorganisms. For the detection of the hemolytic reactions of streptococci and other fastidious microorganisms. The slightly acid pH of this medium enhances distinct hemolytic reactions.
Blood Agar No. 2 Composition per liter: Proteose peptone...............................................15.0g Agar ..................................................................12.0g NaCl....................................................................5.0g Yeast extract........................................................5.0g Liver digest .........................................................2.5g pH 7.4 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems and Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Heat with frequent agitation and boil for 1 min to completely dissolve. Autoclave for 15 min at 15 psi pressure–121°C. Cool the basal medium to 45°–50°C. Aseptically add sterile, defibrinated blood to a final concentration of 7%. Pour into sterile Petri dishes.
Use: For the isolation, cultivation, and detection of hemolytic activity of streptococci, pneumococci, and other particularly fastidious microorganisms.
Blood Base Agar (LMG Medium 45) Composition per liter: Agar ..................................................................15.0g Lab-Lemco beef extract....................................10.0g Special peptones ...............................................10.0g NaCl....................................................................5.0g pH 7.1 ± 0.2 at 25°C
Source: Special peptones is available as a premixed powder from Oxoid Unipath.
Preparation of Medium: Add components to
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Preparation of Medium: Add components, ex-
Use: For the cultivation and maintenance of het-
cept sheep blood, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Heat with frequent agitation and boil for 1 min to completely dissolve. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C. Aseptically add 50.0mL of sterile, defibrinated sheep blood. Mix thoroughly and pour into sterile Petri dishes.
erotrophic bacteria.
Blood Base Agar with Charcoal (LMG Medium 46) Composition per liter: Agar ..................................................................15.0g
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Blood Base Agar with Horse Blood
Lab-Lemco beef extract ....................................10.0g Special peptones ...............................................10.0g NaCl ....................................................................5.0g Charcoal ..............................................................2.0g pH 7.1 ± 0.2 at 25°C
ter and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 50.0mL sterile horse blood. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Source: Special peptones is available as a premixed
Use: For the cultivation and maintenance of fastidi-
powder from Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of various bacteria.
Blood Base Agar with Horse Blood (LMG Medium 47) Composition per liter: Agar ..................................................................15.0g Lab-Lemco beef extract ....................................10.0g Special peptones ...............................................10.0g NaCl ....................................................................5.0g Horse blood, sterile defibrinated................... 50.0mL pH 7.1 ± 0.2 at 25°C
Source: Special peptones is available as a premixed powder from Oxoid Unipath.
Preparation of Medium: Add components, except horse blood, to 950.0mL distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 50.0mL sterile horse blood. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
ous bacteria.
Blood Glucose Cystine Agar Composition per 100.0mL: Nutrient agar ................................................. 85.0mL Glucose cystine solution ............................... 10.0mL Human blood, fresh ........................................ 5.0mL pH 6.8 ± 0.2 at 25°C
Nutrient Agar: Composition per liter: Agar ..................................................................15.0g Pancreatic digest of gelatin.................................5.0g Beef extract.........................................................3.0g
Source: Nutrient agar is available as a premixed powder from BD Diagnostic Systems.
Preparation of Nutrient Agar: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Glucose Cystine Solution: Composition per 50.0mL: Glucose .............................................................12.5g L-Cystine·HCl .....................................................0.5g
Preparation of Glucose Cystine Solution:
Use: For the cultivation and maintenance of fastidi-
Add components to distilled/deionized water and bring volume to 50.0mL. Mix thoroughly. Filter sterilize.
ous bacteria.
Preparation of Medium: To 85.0mL of cooled,
Blood Base Agar with Horse Blood, Fumarate and Formate (LMG Medium 48) Composition per liter: Agar ..................................................................15.0g Lab-Lemco beef extract ....................................10.0g Special peptones, Oxoid ...................................10.0g NaCl ....................................................................5.0g Sodium fumarate.................................................3.0g Sodium formate...................................................2.0g Horse blood, sterile defibrinated................... 50.0mL pH 7.2 ± 0.2 at 25°C
Preparation of Medium: Add components, except horse blood, to 950.0mL distilled/deionized wa-
sterile agar solution, aseptically add 10.0mL of sterile glucose cystine solution and 5.0mL of human blood. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation of Francisella tularensis.
BMPA-α Medium (Edelstein BMPA-α Medium) Composition per liter: Agar ..................................................................13.0g Yeast extract......................................................10.0g ACES buffer (2-[(2-Amino-2-oxoethyl)amino]-ethane sulfonic acid) ........................2.0g Charcoal, activated .............................................2.0g α-Ketoglutarate...................................................0.2g
Bordetella pertussis Selective Medium with Bordet-Gengou Agar Base Fe4(P2O7)3·9H2O...............................................0.05g Antibiotic inhibitor ....................................... 10.0mL L-Cysteine·HCl·H2O solution........................ 10.0mL pH 6.9 ± 0.2 at 25°C
Source: This medium is available as premixed vials from Oxoid Unipath.
Antibiotic Inhibitor: Composition per 10.0mL: Anisomycin.......................................................0.08g Cefamandole ....................................................4.0mg Polymyxin B ................................................80,000U
Preparation of Antibiotic Inhibitor: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. L-Cysteine·HCl·H2O
Solution: Composition per 10.0mL: L-Cysteine·HCl·H2O..........................................0.08g
Preparation of L-Cysteine·HCl·H2O Solution:
Add L-cysteine·HCl·H2O to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except cysteine and antibiotic inhibitor, to distilled/ deionized water and bring volume to 980.0mL. Mix thoroughly. Adjust medium to pH 6.9 with 1N KOH. Heat gently and bring to boiling for 1 min. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°– 55°C. Add 10.0mL of the sterile L-cysteine·HCl·H2O solution and 10.0mL of the sterile antibiotic solution. Mix thoroughly. Pour into sterile Petri dishes with constant agitation to keep charcoal in suspension.
Use: For the selective isolation and cultivation of Legionella pneumophila and other Legionella species.
BMPA-α Medium (Semiselective Medium for Legionella pneumophila) Composition per liter: Agar ..................................................................15.0g Yeast extract......................................................10.0g ACES buffer (2-[(2-Amino-2-oxoethyl)amino]-ethane sulfonic acid) ......................10.0g Charcoal, activated..............................................2.0g α-Ketoglutarate...................................................1.0g Fe4(P2O7)3·9H2O...............................................0.25g Antibiotic inhibitor ....................................... 10.0mL L-Cysteine·HCl·H2O solution........................ 10.0mL pH 6.9 ± 0.2 at 25°C
Antibiotic Inhibitor: Composition per 10.0mL: Anisomycin.......................................................0.08g
69
Cefamandole ....................................................4.0mg Polymyxin B ................................................ 80,000U
Preparation of Antibiotic Inhibitor: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. L-Cysteine·HCl·H2O
Solution: Composition per 10.0mL: L-Cysteine·HCl·H2O............................................0.4g
Preparation of L-Cysteine·HCl·H2O Solution:
Add L-cysteine·HCl·H2O to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except cysteine and antibiotic inhibitor, to distilled/ deionized water and bring volume to 980.0mL. Mix thoroughly. Adjust medium to pH 6.9 with 1N KOH. Heat gently and bring to boiling for 1 min. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°– 55°C. Add 10.0mL of the sterile L-cysteine·HCl·H2O solution and 10.0mL of the sterile antibiotic solution. Mix thoroughly. Pour into sterile Petri dishes with constant agitation to keep charcoal in suspension.
Use: For the selective isolation and cultivation of Legionella pneumophila and other Legionella species.
Bonner-Addicott Medium Composition per liter: Agar ..................................................................25.0g Glucose .............................................................20.0g Ca(NO3)2·4H2O ..............................................0.236g KNO3 ..............................................................0.081g KCl..................................................................0.065g MgSO4·7H2O ..................................................0.036g KH2PO4...........................................................0.012g Ferric tartrate ...................................................1.0mg
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation of a variety of fungi.
Bordetella pertussis Selective Medium with Bordet-Gengou Agar Base Composition per 1210.0mL: Bordet-Gengou agar base .................................. 1.0L Horse blood, defibrinated ........................... 200.0mL Cephalexin solution ...................................... 10.0mL pH 6.7± 0.2 at 25°C
70
Bordetella pertussis Selective Medium with Charcoal Agar Base
Source: This medium is available as a premixed powder from Oxoid Unipath.
Cephalexin Solution: Composition per 10.0mL:
Bordet-Gengou Agar Base: Composition per liter:
Cephalexin ........................................................0.04g
Agar ..................................................................20.0g NaCl ....................................................................5.5g Pancreatic digest of casein..................................5.0g Peptic digest of animal tissue..............................5.0g
cephalexin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Bordet-Gengou Agar Base: Add components to 1.0L of 1% glycerol solution. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C.
Cephalexin Solution: Composition per 10.0mL: Cephalexin ........................................................0.04g
Preparation of Cephalexin Solution: Add cephalexin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. Preparation of Medium: Aseptically add 10.0mL of sterile cephalexin solution and 200.0mL of defibrinated horse blood to 1.0L Bordet-Gengou agar base. Mix thoroughly and pour into sterile Petri dishes.
Use: For the selective isolation and presumptive identification of Bordetella pertussis and Bordetella parapertussis. Bordetella pertussis appears as small, nearly transparent, “bisected pearl-like” colonies.
Preparation of Cephalexin Solution: Add
Preparation of Medium: Aseptically add 10.0mL of sterile cephalexin solution and 100.0mL of defibrinated horse blood to charcoal agar base. Mix thoroughly and pour into sterile Petri dishes.
Use: For the selective isolation and presumptive identification of Bordetella pertussis and Bordetella parapertussis. Bordetella pertussis appears as small, pale, shiny colonies.
Bordet-Gengou Agar Composition per liter: Agar ..................................................................20.0g Glycerol ............................................................10.0g NaCl....................................................................5.5g Pancreatic digest of casein..................................5.0g Peptic digest of animal tissue .............................5.0g Potato, solids from infusion................................4.5g Rabbit blood................................................ 200.0mL pH 6.7± 0.2 at 25°C
Source: This medium is available as a premixed
Bordetella pertussis Selective Medium with Charcoal Agar Base Composition per 1110.0mL: Charcoal agar base ............................................. 1.0L Horse blood, defibrinated ........................... 100.0mL Cephalexin solution ...................................... 10.0mL pH 6.7± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath. Charcoal Agar Base: Composition per liter: Agar ..................................................................12.0g Beef extract .......................................................10.0g Starch ................................................................10.0g NaCl ....................................................................5.0g Pancreatic digest of casein..................................5.0g Peptic digest of animal tissue..............................5.0g Charcoal ..............................................................4.0g Nicotinic acid ...................................................1.0mg
Preparation of Charcoal Agar Base: Add components of charcoal agar base to distilled/deionized water and bring volume to 1.0L. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C.
powder from Oxoid Unipath and BD Diagnostic Systems.
Preparation of Medium: Add 10.0g of glycerol to 980.0mL of distilled/deionized water. Add other components, except rabbit blood, to the glycerol solution. Mix thoroughly. Heat with occasional agitation of the medium. Boil for 1 min. Autoclave for 15 min at 15 psi pressure–121°C. Cool medium to 50°C. Aseptically add 200.0mL of rabbit blood (prewarmed to 35°C) to a concentration of 15–30%. 150.0–200.0mL of sterile, defibrinated horse blood may be used in place of rabbit blood. Mix thoroughly and pour plates or prepare slants. Use: For the detection and isolation of Bordetella pertussis and Bordetella parapertussis from clinical specimens. The medium is rendered selective by the addition of methicillin. Bordetella pertussis appears as small (<1mm), smooth, pearl-like colonies surrounded by a narrow zone of hemolysis. Bordetella parapertussis appears as brown, nonshiny colonies with a green-black coloration on the reverse side. Bordetella bronchiseptica appears as brown, nonshiny, moderately sized colonies with a roughly pitted surface.
Borrelia Medium
Bordet-Gengou Medium (ATCC Medium 35) Composition per liter: Agar ..................................................................20.0g Glycerol ............................................................10.0g Proteose peptone ...............................................10.0g NaCl ....................................................................5.5g Pancreatic digest of casein..................................5.0g Peptic digest of animal tissue..............................5.0g Potato, solids from infusion ................................4.5g Rabbit blood................................................ 150.0mL pH 6.7± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath and BD Diagnostic Systems.
Preparation of Medium: Add 10.0g of glycerol to 980.0mL of distilled/deionized water. Add other components, except rabbit blood, to the glycerol solution. Mix thoroughly. Heat with occasional agitation of the medium. Boil for 1 min. Autoclave for 15 min at 15 psi pressure–121°C. Cool medium to 50°C. Aseptically add 150.0mL of rabbit blood (prewarmed to 35°C). Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes. Allow tubes to cool in a slanted position.
Use: For the detection and isolation of Bordetella pertussis and Bordetella parapertussis from clinical specimens. The medium is rendered selective by the addition of methicillin. Bordetella pertussis appears as small (<1mm), smooth, pearl-like colonies surrounded by a narrow zone of hemolysis. Bordetella parapertussis appears as brown, nonshiny colonies with a green-black coloration on the reverse side. Bordetella bronchiseptica appears as brown, nonshiny, moderately sized colonies with a roughly pitted surface.
Bordet-Gengou Medium (LMG Medium 23) Composition per liter: Agar ..................................................................20.0g Proteose peptone ...............................................10.0g NaCl ....................................................................5.5g Pancreatic digest of casein..................................5.0g Peptic digest of animal tissue..............................5.0g Potato, solids from 125g infusion .......................4.5g Rabbit blood, sterile debrinated .................. 150.0mL Glycerol ........................................................ 10.0mL pH 6.7± 0.2 at 25°C
Preparation of Medium: Add 10.0mL of glycerol to 850.0mL of distilled/deionized water. Add other components, except rabbit blood, to the glycerol solution. Mix thoroughly. Heat with occasional agita-
71
tion of the medium. Boil for 1 min. Autoclave for 15 min at 15 psi pressure–121°C. Cool medium to 45– 50°C. Aseptically add 150.0mL of rabbit blood (prewarmed to 35°C). Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the detection and isolation of Pseudomonas pertucinogena.
Borrelia Medium Composition per 370.0mL: Solution 4.................................................... 240.0mL Solution 1...................................................... 80.0mL Solution 2...................................................... 34.0mL Rabbit serum, sterile ..................................... 10.0mL Solution 3........................................................ 4.0mL Solution 5........................................................ 0.7mL
Solution 1: Composition per liter: Na2HPO4·7H2O...............................................26.52g Glucose ...........................................................12.75g Proteose peptone no.2.......................................5.95g Pancreatic digest of casein................................2.55g NaCl....................................................................1.2g Sodium pyruvate...............................................1.06g NaH2PO4·H2O...................................................1.03g KCl....................................................................0.85g MgCl2·6H2O .....................................................0.68g N-acetylglucosamine.........................................0.53g Sodium citrate·2H2O.........................................0.47g
Preparation of Solution 1: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Store at −20° C.
Solution 2: Composition per 100.0mL: Bovine albumin fraction V ...............................10.0g
Preparation of Solution 2: Add bovine albumin to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Adjust pH to 7.8 with NaOH. Store at −20°C.
Solution 3: Composition per 100.0mL: NaHCO3 ..............................................................4.5g
Preparation of Solution 3: Add NaHCO3 to dis-
tilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Prepare solution freshly.
Solution 4: Composition per 100.0mL: Gelatin.................................................................7.0g
Preparation of Solution 4: Add gelatin to distilled/deionized water and bring volume to 100.0mL.
72
Bouillon Medium
Mix thoroughly. Autoclave for 15 min at 10 psi pressure–115°C. Store at 4°C.
Solution 5: Composition per 100.0mL: Phenol Red..........................................................0.5g
Preparation of Solution 5: Add Phenol Red to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Store at 4°C.
Preparation of Medium: Combine 80.0mL of solution 1, 34.0mL of solution 2, 4.0mL of solution 3, 0.7mL of solution 5, and 1.3mL of distilled/deionized water. Mix thoroughly. Filter sterilize under pressure. Aseptically distribute into sterile borosilicate screwcapped tubes in 6.0mL volumes. Melt solution 4 by immersing tube in warm water. Add 2.0mL of solution 4 to each screw-capped tube. Add 0.5mL of sterile rabbit serum to each screw-capped tube.
Use: For the cultivation of Borrelia hermsii, Borrelia turicatae, and Borrelia parkeri.
Bouillon Medium Composition per liter: Peptone..............................................................15.0g Meat extract ........................................................5.0g NaCl ....................................................................5.0g K2HPO4 ...............................................................5.0g pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Heat with frequent agitation and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the general cultivation of heterotrophic microorganisms.
Bovine Albumin Tween 80 Medium, Ellinghausen and McCullough, Modified (Albumin Fatty Acid Broth, Leptospira Medium) Composition per liter: Basal medium ............................................. 900.0mL Albumin fatty acid supplement................... 100.0mL
Basal Medium: Composition per liter: Na2HPO4, anhydrous ..........................................1.0g NaCl ....................................................................1.0g KH2PO4, anhydrous ............................................0.3g NH4Cl (25% solution)..................................... 1.0mL Glycerol (10% solution).................................. 1.0mL
Sodium pyruvate (10% solution) .................... 1.0mL Thiamine·HCl (0.5% solution) ....................... 1.0mL pH 7.4 ± 0.2 at 25°C
Preparation of Basal Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.4. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C.
Albumin Fatty Acid Supplement: Composition per 200.0mL: Bovine albumin fraction V ...............................20.0g Polysorbate (Tween) 80 (10% solution) ....... 25.0mL FeSO4·7H2O (0.5% solution)........................ 20.0mL CaCl2·2H2O (1.5% solution)........................... 2.0mL MgCl2·2H2O (1.5% solution) ......................... 2.0mL Vitamin B12 (0.2% solution) ........................... 2.0mL ZnSO4·7H2O (0.4% solution) ......................... 2.0mL CuSO4·5H2O (0.3% solution) ......................... 0.2mL
Preparation of Albumin Fatty Acid Supplement: Add bovine albumin to 100.0mL of distilled/ deionized water. Mix thoroughly. Add remaining components while stirring. Adjust pH to 7.4. Bring volume to 200.0mL with distilled/deionized water. Filter sterilize. Store at −20°C.
Preparation of Medium: Aseptically combine 100.0mL of sterile albumin fatty acid supplement and 900.0mL of sterile basal medium. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation of Leptospira species.
Bovine Albumin Tween 80 Semisolid Medium, Ellinghausen and McCullough, Modified (Albumin Fatty Acid Semisolid Medium, Modified) Composition per liter: Basal medium ............................................. 900.0mL Albumin fatty acid supplement................... 100.0mL
Basal Medium: Composition per liter: Agar ....................................................................2.2g Na2HPO4, anhydrous ..........................................1.0g NaCl....................................................................1.0g KH2PO4, anhydrous............................................0.3g NH4Cl (25% solution) .................................... 1.0mL Glycerol (10% solution) ................................. 1.0mL Sodium pyruvate (10% solution) .................... 1.0mL Thiamine·HCl (0.5% solution) ....................... 1.0mL pH 7.4 ± 0.2 at 25°C
Preparation of Basal Medium: Add components to distilled/deionized water and bring volume
Bovine Serum Albumin Tween 80 Broth to 1.0L. Mix thoroughly. Adjust pH to 7.4. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C.
Albumin Fatty Acid Supplement: Composition per 200.0mL: Bovine albumin fraction V ...............................20.0g Polysorbate (Tween) 80 (10% solution) ....... 25.0mL FeSO4·7H2O (0.5% solution)........................ 20.0mL CaCl2·2H2O (1.5% solution)........................... 2.0mL MgCl2·2H2O (1.5% solution).......................... 2.0mL Vitamin B12 (0.2% solution) ........................... 2.0mL ZnSO4·7H2O (0.4% solution) ......................... 2.0mL CuSO4·5H2O (0.3% solution) ......................... 0.2mL
Preparation of Albumin Fatty Acid Supplement: Add bovine albumin to 100.0mL of distilled/
73
Cyanocobalamin (0.02% solution) ................. 1.0mL ZnSO4 (0.4% solution) ................................... 1.0mL
Preparation of Albumin Supplement: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Adjust pH to 7.4. Filter sterilize. MgCl2–CaCl2 Solution: Composition per 100.0mL: CaCl2·2H2O ........................................................1.5g MgCl2·6H2O .......................................................1.5g
Preparation of MgCl2–CaCl2 Solution: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Preparation of Medium: To 900.0mL of cooled,
deionized water. Mix thoroughly. Add remaining components while stirring. Adjust pH to 7.4. Bring volume to 200.0mL with distilled/deionized water. Filter sterilize. Store at −20°C.
sterile basal medium, aseptically add 100.0mL of sterile albumin supplement. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Preparation of Medium: Aseptically combine
tospira species.
100.0mL of sterile albumin fatty acid supplement and 900.0mL of sterile basal medium. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation of Leptospira species.
Use: For the cultivation and maintenance of Lep-
Bovine Serum Albumin Tween 80 Broth (BSA Tween 80 Broth) Composition per liter:
Bovine Serum Albumin Tween 80 Agar (BSA Tween 80 Agar) Composition per liter: Basal medium ............................................. 900.0mL Albumin supplement................................... 100.0mL
Basal Medium: Composition per liter: Agar ..................................................................11.0g Na2HPO4 .............................................................1.0g NaCl ....................................................................1.0g KH2PO4 ...............................................................0.3g Glycerol (10% solution).................................. 1.0mL NH4Cl (25% solution)..................................... 1.0mL Sodium pyruvate (10% solution) .................... 1.0mL Thiamine (0.5% solution) ............................... 1.0mL
Preparation of Basal Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.4. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C.
Albumin Supplement: Composition per 100.0mL: Bovine albumin.................................................10.0g Tween 80 (10% solution) .............................. 12.5mL FeSO4 (0.5% solution) .................................. 10.0mL MgCl2–CaCl2 solution .................................... 1.0mL
Basal medium ............................................. 900.0mL Albumin supplement................................... 100.0mL pH 7.4 ± 0.2 at 25°C
Basal Medium: Composition per liter: Na2HPO4 .............................................................1.0g NaCl....................................................................1.0g KH2PO4...............................................................0.3g Glycerol (10% solution) ................................. 1.0mL NH4Cl (25% solution) .................................... 1.0mL Sodium pyruvate (10% solution) .................... 1.0mL Thiamine (0.5% solution) ............................... 1.0mL
Preparation of Basal Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.4. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C.
Albumin Supplement: Composition per 100.0mL: Bovine albumin.................................................10.0g Tween 80 (10% solution)............................. 12.5mL FeSO4 (0.5% solution).................................. 10.0mL MgCl2-CaCl2 solution..................................... 1.0mL Cyanocobalamin (0.02% solution) ................. 1.0mL ZnSO4 (0.4% solution) ................................... 1.0mL
Preparation of Albumin Supplement: Add components to distilled/deionized water and bring
74
Bovine Serum Albumin Tween 80 Soft Agar
volume to 100.0mL. Mix thoroughly. Adjust pH to 7.4. Filter sterilize.
MgCl2–CaCl2 Solution: Composition per 100.0mL:
MgCl2–CaCl2 Solution: Composition per 100.0mL:
CaCl2·2H2O ........................................................1.5g MgCl2·6H2O .......................................................1.5g
CaCl2·2H2O.........................................................1.5g MgCl2·6H2O .......................................................1.5g
Preparation of MgCl2–CaCl2 Solution: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Preparation of Medium: To 900.0mL of cooled, sterile basal medium, aseptically add 100.0mL of sterile albumin supplement. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the isolation and cultivation of Leptospira species.
Bovine Serum Albumin Tween 80 Soft Agar (BSA Tween 80 Soft Agar) (Semisolid BSA Tween 80 Medium) Composition per liter: Basal medium ............................................. 900.0mL Albumin supplement................................... 100.0mL
Basal Medium: Composition per liter:
Preparation of MgCl2–CaCl2 Solution: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Preparation of Medium: To 900.0mL of cooled, sterile basal medium, aseptically add 100.0mL of sterile albumin supplement. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation of Leptospira species.
Brain Heart CC Agar (Brain Heart Cycloheximide Chloramphenicol Agar) Composition per liter: Pancreatic digest of casein................................16.0g Agar ..................................................................13.5g Brain heart, solids from infusion ........................8.0g Peptic digest of animal tissue .............................5.0g NaCl....................................................................5.0g Na2HPO4 .............................................................2.5g Glucose ...............................................................2.0g Cycloheximide....................................................0.5g Chloramphenicol...............................................0.05g pH 7.4 ± 0.2 at 25°C
Agar ....................................................................2.0g Na2HPO4 .............................................................1.0g NaCl ....................................................................1.0g KH2PO4 ...............................................................0.3g Glycerol (10% solution).................................. 1.0mL NH4Cl (25% solution)..................................... 1.0mL Sodium pyruvate (10% solution) .................... 1.0mL Thiamine (0.5% solution) ............................... 1.0mL
Source: This medium is available as a premixed
Preparation of Basal Medium: Add compo-
genic fungi such as Histoplasma capsulatum and Blastomyces dermatiditis from specimens heavily contaminated with bacteria and other fungi. It may also be used as a base supplemented with sheep blood and gentamicin for enrichment and additional selectivity.
nents to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.4. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C.
Albumin Supplement: Composition per 100.0mL: Bovine albumin.................................................10.0g Tween 80 (10% solution) .............................. 12.5mL FeSO4 (0.5% solution) .................................. 10.0mL CaCl2–MgCl2 solution .................................... 1.0mL Cyanocobalamin (0.02% solution) ................. 1.0mL ZnSO4 (0.4% solution).................................... 1.0mL
Preparation of Albumin Supplement: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Adjust pH to 7.4. Filter sterilize.
powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks while shaking to distribute precipitate. Autoclave for 15 min at 15 psi pressure–118°C.
Use: For the selective isolation of fastidious patho-
Brain Heart Infusion (BHI) Composition per liter: Pancreatic digest of gelatin...............................14.5g Brain heart, solids from infusion ........................6.0g Peptic digest of animal tissue .............................6.0g NaCl....................................................................5.0g Glucose ...............................................................3.0g Na2HPO4 .............................................................2.5g pH 7.4 ± 0.2 at 25°C
Brain Heart Infusion Agar 0.7% Source: This medium is available as a premixed powder from Oxoid Unipath and BD Diagnostic Systems. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of fastidious and nonfastidious microorganisms, including aerobic and anaerobic bacteria, from a variety of clinical and nonclinical specimens. It is particularly useful for culturing streptococci, pneumococci, and meningococci. It is also used for the preparation of inocula for use in antimicrobial susceptibility tests and as a base for blood culture.
Brain Heart Infusion Agar (BHI Agar) Composition per liter: Beef heart infusion..........................................250.0g Calf brain infusion ..........................................200.0g Agar ..................................................................13.5g Proteose peptone ...............................................10.0g NaCl ....................................................................5.0g Na2HPO4·12H2O.................................................2.5g Glucose ...............................................................2.0g pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
75
shaking to distribute precipitate. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of a wide variety of fastidious microorganisms, including bacteria, yeasts, and molds. With the addition of 10% sheep blood, it is used for the isolation and cultivation of many fungal species, including systemic fungi, from clinical and nonclinical specimens. The addition of gentamicin and chloramphenicol with 10% sheep blood produces a selective medium used for the isolation of pathogenic fungi from specimens heavily contaminated with bacteria and saprophtic fungi. It is recommended for the isolation of Histoplasma capsulatum and other pathogenic fungi, including Coccidioides immitis.
Brain Heart Infusion Agar Composition per liter: Agar ..................................................................15.0g Pancreatic digest of gelatin...............................14.5g Brain heart, solids from infusion ........................6.0g Peptic digest of animal tissue .............................6.0g NaCl....................................................................5.0g Glucose ...............................................................3.0g Na2HPO4 .............................................................2.5g pH 7.4 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks while shaking to distribute precipitate. Autoclave for 15 min at 15 psi pressure–121°C. Mix thoroughly. Pour into sterile Petri dishes.
Use: For the cultivation of a variety of fastidious and nonfastidious aerobic and anaerobic microorganisms.
Use: For the cultivation of a wide variety of fastidious
Brain Heart Infusion Agar
Brain Heart Infusion Agar 0.7% (BHI Agar 0.7%)
Composition per liter: Pancreatic digest of casein................................16.0g Agar ..................................................................13.5g Brain heart, solids from infusion ........................8.0g Peptic digest of animal tissue..............................5.0g NaCl ....................................................................5.0g Na2HPO4 .............................................................2.5g Glucose ...............................................................2.0g pH 7.4 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath and BD Diagnostic Systems.
microorganisms, including bacteria, yeasts and molds.
Composition per liter: Pancreatic digest of gelatin...............................14.5g Agar ....................................................................7.0g Brain heart, solids from infusion ........................6.0g Peptic digest of animal tissue .............................6.0g NaCl....................................................................5.0g Glucose ...............................................................3.0g Na2HPO4 .............................................................2.5g pH 5.3 ± 0.2 at 25°C
Source: This medium without agar is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to
Preparation of Medium: Add components, ex-
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks while
cept agar, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 5.3 with
76
Brain Heart Infusion with 0.7% Agar
1N HCl. Mix thoroughly. Add agar. Gently heat and bring to boiling. Distribute into tubes. Autoclave for 10 min at 15 psi pressure–121°C.
tion and sheep blood. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the detection of staphylococcal enterotoxin
ety of fungal species, especially systemic fungi, from clinical and nonclinical specimens. For the selective isolation of pathogenic fungi from specimens heavily contaminated with bacteria and saprophytic fungi. For the maintenance of fungal species on slant cultures.
producing strains.
Brain Heart Infusion with 0.7% Agar Composition per liter: Beef heart infusion..........................................250.0g Calf brain infusion ..........................................200.0g Proteose peptone ...............................................10.0g Agar ....................................................................7.0g NaCl ....................................................................5.0g Na2HPO4·12H2O.................................................2.5g Glucose ...............................................................2.0g pH 5.3 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Adjust pH to 5.3 with 1N HCl. Distribute into tubes in 25.0mL volumes. Autoclave for 10 min at 15 psi pressure–121°C.
Use: For the cultivation of Staphylococcal species for the production of enterotoxin.
Brain Heart Infusion Agar with Chloramphenicol Composition per liter: Pancreatic digest of casein................................16.0g Agar ..................................................................13.5g Brain heart, solids from infusion ........................8.0g Peptic digest of animal tissue..............................5.0g NaCl ....................................................................5.0g Na2HPO4 .............................................................2.5g Glucose ...............................................................2.0g Sheep blood, defibrinated ............................. 50.0mL Chloramphenicol solution............................. 10.0mL pH 7.4 ± 0.2 at 25°C
Chloramphenicol Solution: Composition per 10.0mL: Chloramphenicol...............................................0.05g
Preparation of Chloramphenicol Solution: Add chloramphenicol to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except chloramphenicol solution and sheep blood, to distilled/deionized water and bring volume to 940.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C. Aseptically add sterile chloramphenicol solu-
Use: For the isolation and cultivation of a wide vari-
Brain Heart Infusion Agar with Kanamycin Composition per liter: Pancreatic digest of casein................................16.0g Agar ..................................................................13.5g Brain heart, solids from infusion ........................8.0g Peptic digest of animal tissue .............................5.0g NaCl....................................................................5.0g Na2HPO4 .............................................................2.5g Glucose ...............................................................2.0g Sheep blood, defibrinated ............................. 50.0mL Kanamycin solution ...................................... 10.0mL pH 7.4 ± 0.2 at 25°C
Kanamycin Solution: Composition per 10.0mL: Kanamycin.....................................................25.0mg
Preparation of Kanamycin Solution: Add kanamycin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except kanamycin solution and sheep blood, to distilled/deionized water and bring volume to 940.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile kanamycin solution and sheep blood. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation of fastidious fungi.
Brain Heart Infusion Agar with Penicillin and Streptomycin Composition per liter: Pancreatic digest of casein................................16.0g Agar ..................................................................13.5g Brain heart, solids from infusion ........................8.0g Peptic digest of animal tissue .............................5.0g NaCl....................................................................5.0g Na2HPO4 .............................................................2.5g Glucose ...............................................................2.0g Streptomycin..................................................40.0mg Penicillin ...................................................... 20,000U Sheep blood, defibrinated ............................. 50.0mL pH 7.4 ± 0.2 at 25°C
Brain Heart Infusion with Agar, YE, NaCl, Horse Serum and Penicillin Preparation of Medium: Add components, except sheep blood, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly and while stirring bring to a boil for 1 min to completely dissolve. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 50°C. Aseptically add 50.0mL of defibrinated sheep blood. Mix thoroughly. Pour into sterile Petri dishes while agitating gently to distribute the precipitate through the medium.
Use: For the isolation and cultivation of a wide variety of fungal species, especially systemic fungi, from clinical and nonclinical specimens. For the selective isolation of pathogenic fungi from specimens heavily contaminated with bacteria and saprophytic fungi. For the maintenance of fungal species on slant cultures.
Brain Heart Infusion Agar with 10% Sheep Blood, Gentamicin, and Chloramphenicol Composition per liter: Pancreatic digest of casein................................16.0g Agar ..................................................................13.5g Brain heart, solids from infusion ........................8.0g Peptic digest of animal tissue..............................5.0g NaCl ....................................................................5.0g Na2HPO4 .............................................................2.5g Glucose ...............................................................2.0g Sheep blood, defibrinated ........................... 100.0mL Antibiotic solution ........................................ 10.0mL pH 7.4 ± 0.2 at 25°C
Antibiotic Solution: Composition per 10.0mL: Chloramphenicol...............................................0.05g Gentamicin........................................................0.05g
Preparation of Antibiotic Solution: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except antibiotic solution and sheep blood, to distilled/ deionized water and bring volume to 890.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile antibiotic solution and sheep blood. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation and cultivation of a wide variety of fungal species, especially systemic fungi, from clinical and nonclinical specimens. For the selective isolation of pathogenic fungi from specimens heavily contaminated with bacteria and saprophytic fungi. For the maintenance of fungal species on slant cultures.
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Brain Heart Infusion Agar with Tween 80 (ATCC Medium 1941) Composition per liter: Pancreatic digest of casein................................16.0g Agar ..................................................................13.5g Brain heart, solids from infusion ........................8.0g Peptic digest of animal tissue .............................5.0g NaCl....................................................................5.0g Na2HPO4 .............................................................2.5g Glucose ...............................................................2.0g Tween 80.............................................................1.0g pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks while shaking to distribute precipitate. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation of Helicococcus kunzii.
Brain Heart Infusion with Agar, Yeast Extract, NaCl, Inactivated Horse Serum, and Penicillin Composition per liter: NaCl..................................................................20.0g Pancreatic digest of gelatin...............................14.5g Agar ..................................................................12.0g Brain heart, solids from infusion ........................6.0g Peptic digest of animal tissue .............................6.0g Yeast extract........................................................5.0g NaCl....................................................................5.0g Glucose ...............................................................3.0g Na2HPO4 .............................................................2.5g Horse serum, inactivated ............................ 100.0mL Penicillin solution ......................................... 10.0mL pH 7.4 ± 0.2 at 25°C
Penicillin Solution: Composition per 10.0mL: Penicillin ................................................. 1,000,000U
Preparation of Penicillin Solution: Add penicillin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except penicillin solution and inactivated horse serum, to distilled/deionized water and bring volume to 890.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°– 50°C. Aseptically add sterile penicillin solution and horse serum. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation of fastidious fungi.
78
Brain Heart Infusion with Agar, YE, Sucrose, Horse Serum, and Penicillin Brain Heart Infusion with Agar, Yeast Extract, Sucrose, Horse Serum, and Penicillin
Composition per liter:
Preparation of Penicillin Solution: Add penicillin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, ex-
Sucrose............................................................100.0g Pancreatic digest of gelatin ...............................14.5g Agar ..................................................................12.0g Brain heart, solids from infusion ........................6.0g Peptic digest of animal tissue..............................6.0g Yeast extract........................................................5.0g NaCl ....................................................................5.0g Glucose ...............................................................3.0g Na2HPO4 .............................................................2.5g Horse serum ................................................ 100.0mL Penicillin solution ......................................... 10.0mL pH 7.4 ± 0.2 at 25°C
cept penicillin solution and inactivated horse serum, to distilled/deionized water and bring volume to 890.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C. Aseptically add sterile penicillin solution and horse serum. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Penicillin Solution: Composition per 10.0mL:
Blood agar.......................................................... 1.1L Overlay solution................................................. 1.0L pH 7.4 ± 0.2 at 25°C
Penicillin ....................................................100,000U
Preparation of Penicillin Solution: Add penicillin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except penicillin solution and horse serum, to distilled/ deionized water and bring volume to 890.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile penicillin solution and horse serum. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation of fastidious fungi.
Brain Heart Infusion with Agar, Yeast Extract, Sucrose, Inactivated Horse Serum, and Penicillin Composition per liter: Sucrose............................................................100.0g Pancreatic digest of gelatin ...............................14.5g Agar ..................................................................12.0g Brain heart, solids from infusion ........................6.0g Peptic digest of animal tissue..............................6.0g Yeast extract........................................................5.0g NaCl ....................................................................5.0g Glucose ...............................................................3.0g Na2HPO4 .............................................................2.5g Horse serum, inactivated............................. 100.0mL Penicillin solution ......................................... 10.0mL pH 7.4 ± 0.2 at 25°C
Penicillin Solution: Composition per 10.0mL: Penicillin .................................................1,000,000U
Use: For the cultivation of fastidious fungi.
Brain Heart Infusion Blood Agar Composition per liter:
Blood Agar: Composition per liter: Agar ..................................................................18.0g Pancreatic digest of gelatin...............................14.5g Brain heart, solids from infusion ........................6.0g Peptic digest of animal tissue .............................6.0g NaCl....................................................................5.0g Glucose ...............................................................3.0g Na2HPO4 .............................................................2.5g Rabbit blood, defibrinated .......................... 100.0mL
Preparation of Blood Agar: Add components, except rabbit blood, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat and bring to boiling. Adjust pH to 7.4. Distribute 5.0mL of agar solution into tubes. Autoclave for 25 min at 15 psi pressure–121°C. Cool to 50°C. Aseptically add 0.5mL of sterile rabbit blood to each tube. Mix thoroughly. Allow tubes to cool in a slanted position.
Overlay Solution: Composition per liter: Pancreatic digest of gelatin...............................14.5g Brain heart, solids from infusion ........................6.0g Peptic digest of animal tissue .............................6.0g NaCl....................................................................5.0g Glucose ...............................................................3.0g Na2HPO4 .............................................................2.5g
Preparation of Overlay Solution: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure– 121°C.
Brain Heart Infusion with Cystine Preparation of Medium: Prior to inoculation, add 0.5mL of overlay solution to the surface of solidified blood agar slants. Use: For the cultivation of Leishmania aethiopica, Leishmania amazonensis, Leishmania aristedesi, Leishmania braziliensis, Leishmania chagasi, Leishmania donovani, Leishmania enriettii, Leishmania garnhami, Leishmania gerbilli, Leishmania guyanensis, Leishmania hertigi, Leishmania infantum, Leishmania major, Leishmania mexicana, Leishmania panamensis, Leishmania pifanoi, Leishmania tropica, and Trypanosoma conorrhini.
Brain Heart Infusion Broth (BHI Broth) Composition per liter: Beef heart infusion..........................................250.0g Calf brain infusion ..........................................200.0g Proteose peptone ...............................................10.0g NaCl ....................................................................5.0g Na2HPO4·12H2O.................................................2.5g Glucose ...............................................................2.0g pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of a variety of fastidious and nonfastidious aerobic and anaerobic microorganisms.
Brain Heart Infusion Broth Composition per liter: Beef heart infusion..........................................250.0g Calf brain infusion ..........................................200.0g Proteose peptone ...............................................10.0g NaCl ....................................................................5.0g Na2HPO4 .............................................................2.5g Glucose ...............................................................2.0g pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks while shaking to distribute precipitate. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of a wide variety of microorganisms, including bacteria, yeasts, and molds, especially fastidious species.
Brain Heart Infusion Broth (BHI Broth) Composition per liter: Beef heart infusion..........................................250.0g Calf brain infusion ..........................................200.0g
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Proteose peptone...............................................10.0g NaCl....................................................................5.0g Na2HPO4·12H2O.................................................2.5g Glucose ...............................................................2.0g pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of a variety of fastidious and nonfastidious aerobic and anaerobic microorganisms.
Brain Heart Infusion with Casein Composition per liter: Pancreatic digest of gelatin...............................14.5g Brain heart, solids from infusion ........................6.0g Peptic digest of animal tissue .............................6.0g NaCl....................................................................5.0g Casein .................................................................5.0g Glucose ...............................................................3.0g Na2HPO4 .............................................................2.5g pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of Serratia marcescens.
Brain Heart Infusion Casein Starch Composition per liter: Pancreatic digest of gelatin...............................14.5g Casein hydrolysate............................................10.0g Brain heart, solids from infusion ........................6.0g Peptic digest of animal tissue .............................6.0g NaCl....................................................................5.0g Glucose ...............................................................3.0g Na2HPO4 .............................................................2.5g Soluble starch......................................................1.0g pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of Actinomyces odontolyticus.
Brain Heart Infusion with Cystine Composition per liter: Pancreatic digest of gelatin...............................14.5g Brain heart, solids from infusion ........................6.0g Peptic digest of animal tissue .............................6.0g NaCl....................................................................5.0g Glucose ...............................................................3.0g
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Brain Heart Infusion with Glucose and Horse Serum
Na2HPO4 .............................................................2.5g Cystine ................................................................1.0g pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of Blastomyces dermatitidis, Histoplasma capsulatum, Mucor hiemalis, Paracoccidioides brasiliensis, and Sporothrix schenckii.
Brain Heart Infusion with Glucose and Horse Serum (LMG Medium 183) Composition per 1300.0mL: Brain heart infusion agar.................................... 1.0L Horse serum ................................................ 200.0mL Glucose solution ......................................... 100.0mL pH 7.4 ± 0.2 at 25°C
Brain Heart Infusion Agar: Composition per liter: Beef heart infusion..........................................250.0g Calf brain infusion ..........................................200.0g Agar ..................................................................13.5g Proteose peptone ...............................................10.0g NaCl ....................................................................5.0g Na2HPO4·12H2O.................................................2.5g Glucose ...............................................................2.0g
Preparation of Brain Heart Infusion Agar: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Glucose Solution: Composition per 100.0mL: Glucose .............................................................10.0g
Preparation of Glucose Solution: Add glucose to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize. Preparation of Medium: Aseptically add 200.0mL sterile horse serum and 100.0mL sterile glucose solution to 1.0L sterile brain heart infusion agar. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation of Streptococcus pyogenes.
Brain Heart Infusion with 5% NaCl Composition per liter: NaCl ..................................................................50.0g Pancreatic digest of gelatin ...............................14.5g
Brain heart, solids from infusion ........................6.0g Peptic digest of animal tissue .............................6.0g Glucose ...............................................................3.0g Na2HPO4 .............................................................2.5g pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of Pediococcus halophilus.
Brain Heart Infusion with PABA (Brain Heart Infusion with p-Aminobenzoic Acid) Composition per liter: Pancreatic digest of gelatin...............................14.5g Brain heart, solids from infusion ........................6.0g Peptic digest of animal tissue .............................6.0g NaCl....................................................................5.0g Glucose ...............................................................3.0g Na2HPO4 .............................................................2.5g p-Aminobenzoic acid........................................0.05g pH 7.4 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. The addition of 1.0g agar to the medium enhances the growth of anaerobic and microaerophilic microorganisms. Heat with frequent agitation and boil for 1 min to dissolve. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the detection of microorganisms in the blood of patients who have received sulfonamide therapy.
Brain Heart Infusion with PABA and Agar (Brain Heart Infusion with p-Aminobenzoic Acid and Agar) Composition per liter: Pancreatic digest of gelatin...............................14.5g Brain heart, solids from infusion ........................6.0g Peptic digest of animal tissue .............................6.0g NaCl....................................................................5.0g Glucose ...............................................................3.0g Na2HPO4 .............................................................2.5g Agar ....................................................................1.0g p-Aminobenzoic acid........................................0.05g pH 7.4 ± 0.2 at 25°C
Brain Heart Infusion Soil Extract Medium Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. The addition of 1.0g of agar to the medium enhances the growth of anaerobic and microaerophilic microorganisms. Heat with frequent agitation and boil for 1 min to dissolve. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the detection of microorganisms in the blood of patients who have received sulfonamide therapy.
Brain Heart Infusion with Rabbit Serum Composition per liter: Yeast extract......................................................20.0g Pancreatic digest of casein................................16.0g Brain heart, solids from infusion ........................8.0g Peptic digest of animal tissue..............................5.0g NaCl ....................................................................5.0g Na2HPO4 .............................................................2.5g Glucose ...............................................................2.0g Rabbit serum, heat inactivated...................... 50.0mL Nicotinamide adenine dinucleotide solution .............................. 10.0mL pH 7.2 ± 0.2 at 25°C
Nicotinamide Adenine Dinucleotide Solution: Composition per 10.0mL: Nicotinamide adenine dinucleotide ....................0.1g
Preparation of Nicotinamide Adenine Dinucleotide Solution: Add 0.1g of nicotinamide ade-
81
Peptic digest of animal tissue .............................6.0g Glucose ...............................................................3.0g Na2HPO4 .............................................................2.5g pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of Vibrio parahaemolyticus.
Brain Heart Infusion Soil Extract Medium Composition per liter: Yeast extract......................................................20.0g Pancreatic digest of casein................................16.0g Brain heart, solids from infusion ........................8.0g Peptic digest of animal tissue .............................5.0g NaCl....................................................................5.0g Na2HPO4 .............................................................2.5g Glucose ...............................................................2.0g Soil extract .................................................. 250.0mL Vitamin B12 solution ....................................... 1.0mL pH 7.2 ± 0.2 at 25°C
Soil Extract: Composition per 400.0mL: African Violet soil...............................................1.0g Na2CO3 ...............................................................1.0g
Preparation of Soil Extract: Autoclave for 60 min at 15 psi pressure–121°C. Filter through paper before using in medium.
nine dinucleotide to distilled/deinonized water and bring volume to 10.0mL. Filter sterilize.
Vitamin B12 Solution: Composition per 1.0mL:
Preparation of Medium: Add components, ex-
Vitamin B12 .......................................................2.0µg
cept nicotinamide adenine dinucleotide solution and rabbit serum, to distilled/deionized water and bring volume to 940.0mL. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Aseptically add 10.0mL of a 0.1% filter-sterilized solution of nicotinamide adenine dinucleotide. Aseptically add 50.0mL of heat-inactivated rabbit serum. Distribute aseptically into tubes or flasks.
Preparation of Vitamin B12 Solution: Add vi-
Use: For the cultivation and maintenance of Actinobacillus species.
Brain Heart Infusion with 3% Sodium Chloride Composition per liter: NaCl ..................................................................30.0g Pancreatic digest of gelatin ...............................14.5g Brain heart, solids from infusion ........................6.0g
tamin B12 to distilled/deionized water and bring volume to 1.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except glucose, yeast extract, and vitamin B12 solution, to tap water and bring volume to 799.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure– 121°C. Add yeast extract and glucose to 200.0mL of tap water. Filter sterilize and add aseptically to cooled, sterile basal medium. Aseptically add 1.0mL of vitamin B12 solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation of a wide variety of microorganisms, including bacteria, yeasts, and molds, especially fastidious species from soil. For the isolation of Histoplasma capsulatum and other pathogenic fungi, including Coccidioides immitis.
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Brain Heart Infusion with Sucrose and Horse Serum
Brain Heart Infusion with Sucrose and Horse Serum Composition per liter: Sucrose............................................................171.0g Pancreatic digest of gelatin ...............................14.5g Brain heart, solids from infusion ........................6.0g Peptic digest of animal tissue..............................6.0g NaCl ....................................................................5.0g Glucose ...............................................................3.0g Na2HPO4 .............................................................2.5g Horse serum ................................................ 100.0mL pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components, except horse serum, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C. Aseptically add 100.0mL sterile horse serum. Mix thoroughly. Distribute into sterile tubes or flasks.
Use: For the cultivation of fastidious fungi.
Brain Liver Heart Semisolid Medium Composition per liter: Beef heart, infusion from ................................250.0g Calf brains, infusion from...............................200.0g Liver, infusion from ..........................................50.0g Proteose peptone ...............................................10.0g NaCl ....................................................................5.0g Neopeptone .......................................................3.25g Pancreatic digest of casein................................3.25g Na2HPO4 .............................................................2.5g Glucose ...............................................................2.0g Agar ..................................................................1.75g pH 7.3 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Leave in tubes.
Use: For the cultivation of fastidious microorganisms. For the cultivation of Actinomyces bovis, Actinomyces israelii, and Actinomyces naeslundii.
Brewer Anaerobic Agar Composition per liter: Agar ..................................................................20.0g Proteose peptone no. 3 ......................................10.0g Glucose .............................................................10.0g Pancreatic digest of casein..................................5.0g Yeast extract........................................................5.0g NaCl ....................................................................5.0g Sodium thioglycolate ..........................................2.0g
Sodium formaldehyde sulfoxylate......................1.0g Resazurin .........................................................2.0mg pH 7.2 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation and maintenance of anaerobic and microaerophilic microorganisms.
Brewer Thioglycolate Medium Composition per liter: Beef, infusion from.........................................500.0g Proteose peptone...............................................10.0g NaCl....................................................................5.0g Glucose ...............................................................5.0g K2HPO4...............................................................2.0g Sodium thioglycolate ..........................................0.5g Agar ....................................................................0.5g Methylene Blue................................................2.0mg pH 7.2 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation and maintenance of anaerobic and microaerophilic microorganisms. For testing the sterility of biological products and materials.
Brewer Thioglycolate Medium, Modified Composition per liter: Tryptic digest of casein.....................................17.0g Glucose .............................................................10.0g NaCl....................................................................5.0g Enzymatic hydrolysate of soybean meal ............3.0g K2HPO4...............................................................2.0g Sodium thioglycolate ..........................................1.0g Agar ....................................................................0.5g Methylene Blue................................................2.0mg pH 7.2 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat to boiling. Distribute into
Brilliant Green Agar, Modified tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation and maintenance of anaerobic and microaerophilic microorganisms. For testing the sterility of biological products and materials.
BRILA MUG Broth (Brillant Green 2%-Bile MUG Broth) Composition per liter: Ox-bile (dried) ..................................................20.0g Peptone..............................................................10.0g Lactose ..............................................................10.0g L-Tryptophan.......................................................1.0g Brillant Green .................................................0.133g 4-Methylumbelliferyl-ß-D-glucuronide..............0.1g pH 7.2 ± 0.2 at 37°C
Source: This medium is available from Fluka, Sig-
83
Source: This medium is available as a premixed powder from Oxoid Unipath and BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes.
Use: For the selective isolation of Salmonella other than Salmonella typhi from feces and other specimens. Salmonella other than Salmonella typhi appear as red/ pink/white colonies surrounded by a zone of red in the agar, indicating nonlactose/sucrose fermentation. Proteus or Pseudomonas species may appear as small red colonies. Lactose- or sucrose-fermenting bacteria appear as yellow-green colonies surrounded by a zone of yellow-green in the agar.
Brilliant Green Agar, Modified
ma-Aldrich.
Composition per liter:
Preparation of Medium: Add components to
Agar ..................................................................12.0g Lactose..............................................................10.0g Sucrose..............................................................10.0g Beef extract.........................................................5.0g Peptone ...............................................................5.0g NaCl....................................................................5.0g Yeast extract........................................................3.0g Na2HPO4 .............................................................1.0g NaH2PO4 .............................................................0.6g Phenol Red........................................................0.09g Brilliant Green .................................................4.7mg pH 6.9 ± 0.2 at 25°C
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into test tubes that contain an inverted Durham tube in 10.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the detection of E. coli and coliforms. Bile and brilliant green extensively inhibit the growth of accompanying flora, in particular gram-positive microorganisms. The presence of E. coli results in fluorescence in the UV. A positive indole test and possibly gas formation from lactose fermentation provide confirmation. β-D-glucoronidase, which is produced by E. coli, cleaves 4-Methylumbelliferyl-β-D-glucuronide to 4-methylumbelliferone and glucuronide. The fluorogen 4-methylumbelliferone can be detected under a long wavelength UV lamp.The broth can be used in conjunction with the MPN method for E. coli and coliform enumeration in the water of bathing areas.
Brilliant Green Agar Composition per liter: Agar ..................................................................20.0g Lactose ..............................................................10.0g Sucrose..............................................................10.0g Peptic digest of animal tissue..............................5.0g Pancreatic digest of casein..................................5.0g NaCl ....................................................................5.0g Phenol Red........................................................0.08g Brilliant Green ..............................................0.0125g pH 6.9 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring volume to1.0L. Mix thoroughly. Gently heat and bring to boiling. Do not autoclave. Cool to 45°–50°C. Addition of 1.0g of sodium sulfacetamide and 250.0mg of sodium mandelate enhances inhibition of contaminating microorganisms. Pour into sterile Petri dishes.
Use: For the selective isolation of Salmonella other than Salmonella typhi from feces. Salmonella other than Salmonella typhi appear as red/pink/white colonies surrounded by a zone of red in the agar, indicating nonlactose/sucrose fermentation. Proteus or Pseudomonas species may appear as small red colonies. Lactose- or sucrose-fermenting bacteria appear as yellow-green colonies surrounded by a zone of yellow-green in the agar.
84
Brilliant Green 2%-Bile Broth, Fluorocult®
Brilliant Green 2%-Bile Broth, Fluorocult® (Fluorocult Brilliant Green 2%-Bile Broth) (BRILA) Composition per liter: Ox bile, dried ....................................................20.0g Peptone..............................................................10.0g Lactose ..............................................................10.0g L-Tryptophan.......................................................1.0g 4-Methylumbelliferyl-β-D-glucuronide ..............0.1g Brilliant Green ..............................................0.0133g pH 7.2 ± 0.2 at 25°C
Source: This medium is available from Merck. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Cool. Distribute into test tubes containing inverted Durham tubes. Autoclave for 15 min at 15 psi pressure–121°C. Do not autoclave longer. The prepared broth is clear and green.
Use: For the cultivation of Escherichia coli. Bile and brilliant green almost completely inhibit the growth of undesired microbial flora, in particular Gram-positive microorganisms. E. coli shows a positive fluorescence under UV light (366 nm). A positive indole reaction and, if necessary gas formation due to fermenting lactose, confirm the findings.
Brilliant Green Lactose Bile Broth Composition per liter:
15 psi pressure–121°C. After sterilization, cool the broth rapidly. Medium is sensitive to light.The final pH should be 7.2 ± 0.1 at 25°C.
Use: For the detection of coliform microorganisms. Turbidity in the broth and gas in the Durham tube are positive indications of Escherichia coli.
Brilliant Green Phenol Red Agar Composition per liter: Agar ..................................................................15.0g Lactose..............................................................15.0g Peptone .............................................................10.0g Meat extract ........................................................5.0g NaCl....................................................................5.0g Phenol Red........................................................0.08g Brilliant Green ............................................. 0.0125g pH 6.9 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation of Salmonella species.
BROLACIN MUG Agar (Bromthymol Blue Lactose Cystine MUG Agar) (C.L.E.D. MUG Agar) Composition per liter:
Source: This medium is available as a premixed powder from BD Diagnostic Systems and Oxoid Unipath.
Agar ..................................................................12.0g Lactose..............................................................10.0g Universal peptone ...............................................4.0g Casein peptone....................................................4.0g Meat extract ........................................................3.0g L-Cystine.........................................................0.128g 4-Methylumbelliferyl-β-D-glucuronide ..............0.1g Bromthymol Blue .............................................0.02g pH 7.3 ± 0.2 at 37°C
Preparation of Medium: Add lactose and pan-
Source: This medium is available from Fluka, Sig-
Oxgall, dehydrated............................................20.0g Lactose ..............................................................10.0g Pancreatic digest of gelatin ...............................10.0g Brilliant Green ..............................................0.0133g pH 7.2 ± 0.1 at 25°C
creatic digest of gelatin to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Add 20.0g oxgall dissolved in 200.0mL distilled/deionized water. The pH of this solution should be 7.0-7.5. Mix thoroughly. Bring volume to 975.0mL with distilled/deionized water. Adjust pH to 7.4. Add 13.3mL of 0.1% aqueous Brilliant Grenn in distilled/deionized water. Adjust volume to 1.0L with distilled/ deionized water. Distribute into tubes containing inverted Durham tubes, in 10.0mL amounts for testing 1.0mL or less of sample. Make sure that the fluid level covers the inverted vials. Autoclave for 15 min at
ma-Aldrich.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 50°C. Pour into sterile Petri dishes.
Use: For the enumeration, isolation, and identification of microorganisms in urine. Growth of all urinary microorganisms is favored. Lactose catabolism produces a color change of Bromthymol Blue to yellow. Alkalization gives a color change to deep-blue.
Bromthymol Blue Agar β-D-glucoronidase, which is produced by E. coli, cleaves 4-methylumbelliferyl-β-D-glucuronide to 4methylumbelliferone and glucuronide. The fluorogen 4-methylumbelliferone can be detected under a long wavelength UV lamp, permitting differentiation of E. coli colonies.
Bromcresol Purple Broth Composition per liter: Peptone..............................................................10.0g NaCl ....................................................................5.0g Beef extract .........................................................3.0g Bromcresol Purple ............................................0.04g Carbohydrate solution................................... 10.0mL pH 7.0 ± 0.2 at 25°C
Carbohydrate Solution: Composition per 10.0mL: Carbohydrate.......................................................5.0g
Preparation of Carbohydrate Solution: Add carbohydrate to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components to
85
cally add 50.0mL of carbohydrate solution. Aseptically distribute into tubes or flasks. Alternately distribute the medium without the carbohydrate solution into test tubes that contain an inverted Durham tube prior to autoclaving. Then autoclave for 10 min at 15 psi pressure–121°C, cool to 25°C, and aseptically add the carbohydrate solution to each tube to yield a final carbohydrate concentration of 5%.
Use: For the differentiation of a variety of microorganisms based on their fermentation of specific carbohydrates. Bacteria that ferment the specific carbohydrate turn the medium yellow. When bacteria produce gas, the gas is trapped in the Durham tube.
Bromcresol Purple Dextrose Broth (BCP Broth) Composition per liter: Glucose .............................................................10.0g Peptone ...............................................................5.0g Beef extract.........................................................3.0g Bromcresol Purple solution ............................ 2.0mL pH 7.0 ± 0.2 at 25°C
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into test tubes that contain an inverted Durham tube. Autoclave for 10 min at 15 psi pressure–121°C.
Bromcresol Purple Solution: Composition per 10.0mL:
Use: For the differentiation of a variety of microor-
Add Bromcresol Purple to 10.0mL of ethanol. Mix thoroughly.
ganisms based on their fermentation of specific carbohydrates. Bacteria that ferment the specific carbohydrate turn the medium yellow. When bacteria produce gas, the gas is trapped in the Durham tube.
Bromcresol Purple Broth Composition per liter: Peptone..............................................................10.0g NaCl ....................................................................5.0g Beef extract .........................................................3.0g Bromcresol Purple ............................................0.04g Carbohydrate solution................................... 50.0mL pH 7.0 ± 0.2 at 25°C
Carbohydrate Solution: Composition per 50.0mL: Carbohydrate.....................................................25.0g
Preparation of Carbohydrate Solution: Add carbohydrate to distilled/deionized water and bring volume to 50.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except carbohydrate solution, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 10 min at 15 psi pressure–121°C. Cool to 25°C. Asepti-
Bromcresol Purple ............................................0.16g Ethanol (95% solution) ................................. 10.0mL
Preparation of Bromcresol Purple Solution:
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes in 12–15mL volumes. Autoclave for 15 min at 15 psi pressure– 121°C.
Use: For the cultivation and differentiation of bacteria based on their ability to ferment glucose. Bacteria that ferment glucose turn the medium yellow.
Bromthymol Blue Agar Composition per liter: Agar .................................................................. 11.0g Peptone .............................................................10.0g NaCl....................................................................5.0g Yeast extract........................................................5.0g Lactose (33% solution) ................................. 27.0mL Bromthymol Blue (1% solution) .................. 10.0mL Sodium thiosulfate (50% solution) ................. 2.0mL Glucose (33% solution) .................................. 1.2mL Maranil solution (5% solution)....................... 1.0mL pH 7.7–7.8 at 25°C
Preparation of Medium: Add agar, peptone, NaCl, and yeast extract to distilled/deionized water
86
Bromthymol Blue Broth
and bring volume to 1.0L. Mix thoroughly. Adjust pH to 8.0. Autoclave for 20 min at 15 psi pressure–121°C. Cool to 45°–50°C. Filter sterilize separately the lactose solution, Bromthymol Blue solution, sodium thiosulfate solution, glucose solution, and maranil solution. To the cooled, sterile agar solution aseptically add 27.0mL of sterile lactose solution, 10.0mL of sterile Bromthymol Blue solution, 2.0mL of sterile sodium thiosulfate solution, 1.2mL of sterile glucose solution, and 1.0mL of sterile maranil solution. Mix thoroughly. Adjust pH to 7.7–7.8. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the selective isolation and cultivation of members of the Enterobacteriaceae.
Nystatin Solution: Composition per 1.0mL: Nystatin........................................................ 50,000U
Preparation of Nystatin Solution: Add nystatin to distilled/deionized water and bring volume to 1.0mL. Filter sterilize. Tripeptide Solution: Composition per 10.0mL: Glycyl-L-histidyl-L-lysine acetate ....................0.2mg
Preparation of Tripeptide Solution: Add glycyl-L-histidyl-L-lysine acetate to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. Store at −20°C.
Preparation of Medium: Add components—ex-
Bromthymol Blue Broth Composition per 101.45mL: Pancreatic digest of casein..................................0.7g NaCl ....................................................................0.5g Beef extract .........................................................0.3g Yeast extract........................................................0.3g Beef heart, solids from infusion..........................0.2g Horse serum .................................................. 10.0mL Bromthymol Blue solution.............................. 1.0mL Ampicillin solution ......................................... 1.0mL Urea solution................................................. 0.25mL Nystatin solution ............................................. 0.1mL Tripeptide solution .......................................... 0.1mL pH 6.0 ± 0.2 at 25°C
Bromthymol Blue Solution: Composition per 50.0mL: Bromthymol Blue ...............................................0.2g NaOH (0.01N solution)................................. 32.0mL
Preparation of Bromthymol Blue Solution: Add Bromthymol Blue to NaOH solution. Mix thoroughly. Bring volume to 50.0mL with distilled/ deionized water. Autoclave for 15 min at 15 psi pressure–121°C. Store at 25°C.
Ampicillin Solution: Composition per 10.0mL:
cept horse serum, ampicillin solution, urea solution, nystatin solution, and tripeptide solution—to distilled/deionized water and bring volume to 90.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 10.0mL of sterile horse serum, 1.0mL of sterile ampicillin solution, 0.25mL of sterile urea solution, 0.1mL of sterile nystatin solution, and 0.1mL of sterile tripeptide solution. Mix thoroughly. Pour into sterile Petri dishes.
Use: For the cultivation of Ureaplasma species from clinical specimens.
Brucella Agar Composition per liter: Agar ..................................................................15.0g Pancreatic digest of casein................................10.0g Peptic digest of animal tissue ...........................10.0g NaCl....................................................................5.0g Yeast extract........................................................2.0g Glucose ...............................................................1.0g NaHSO3 ..............................................................0.1g Horse blood, defibrinated ........................... 100.0mL pH 7.0 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems and Oxoid Unipath.
Ampicillin ...........................................................1.0g
Preparation of Medium: Add components to
Preparation of Ampicillin Solution: Add
distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Heat gently with frequent mixing. Boil for 1 min. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Add 100.0mL of sterile defibrinated horse blood. Mix gently and pour into sterile Petri dishes.
ampicillin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Urea Solution: Composition per 100.0mL: Urea...................................................................10.0g
Preparation of Urea Solution: Add urea to distilled/deionized water and bring volume to 100.0mL. Filter sterilize. Store at −20°C.
Use: For the cultivation and maintenance of Brucella species. For the isolation and cultivation of nonfastidious and fastidious microorganisms from a variety of clinical and nonclinical specimens.
Brucella Albimi Broth with 0.16% Agar and 1% Glycine
Brucella Agar Base Campylobacter Medium Composition per 1100.0mL: Cycloheximide (actidione)................................0.05g Sodium cephazolin..........................................0.015g Novobiocin.......................................................5.0mg Bacitracin .....................................................25,000U Colistin sulfate .............................................10,000U Brucella agar base.............................................. 1.0L Horse blood, defibrinated ........................... 100.0mL
Brucella Agar Base Composition per liter: Agar ..................................................................15.0g Pancreatic digest of casein................................10.0g Peptic digest of animal tissue............................10.0g NaCl ....................................................................5.0g Yeast extract........................................................2.0g Glucose ...............................................................1.0g NaHSO3 ..............................................................0.1g
Preparation of Brucella Agar Base: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly.
Optional Supplement: Composition per 10.0mL:
87
Sheep blood, defibrinated ............................. 50.0mL Vitamin K1 solution ........................................ 1.0mL pH 7.0 ± 0.2 at 25°C
Vitamin K1 Solution: Composition per 20.0mL: Vitamin K1 ..........................................................0.2g Ethanol, absolute........................................... 20.0mL
Preparation of Vitamin K1 Solution: Add vita-
min K1 to 20.0mL of ethanol. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except sheep blood and vitamin K1 solution, to distilled/deionized water and bring volume to 949.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 50.0mL of sterile sheep blood and 1.0mL of sterile vitamin K1 solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation of Brucella species.
Brucella Albimi Broth with 0.16% Agar Composition per liter:
Preparation of Optional Supplement: Add components to distilled/deionized water and bring volume to 10.0mL. Filter sterilize.
Pancreatic digest of casein................................10.0g Peptic digest of animal tissue ...........................10.0g NaCl....................................................................5.0g Yeast extract........................................................2.0g Agar ....................................................................1.6g Glucose ...............................................................1.0g NaHSO3 ..............................................................0.1g Horse blood, defibrinated ........................... 100.0mL pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Add components to
Preparation of Medium: Add components, ex-
Sodium pyruvate ...............................................0.25g NaHSO3 ............................................................0.25g FeSO4·7H2O......................................................0.25g
1.0L of prepared Brucella agar base. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Add 100.0mL of sterile, defibrinated horse blood. Addition of 10.0mL of optional supplement will improve growth. Mix thoroughly. Pour into sterile Petri dishes.
Use: For the selective isolation and cultivation of
cept horse blood, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Heat gently with frequent mixing. Boil for 1 min. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°– 50°C. Aseptically add 100.0mL of sterile defibrinated horse blood. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Campylobacter jejuni from fecal specimens or rectal swabs.
Use: For the cultivation and maintenance of Campy-
Brucella Agar with Vitamin K1
Brucella Albimi Broth with 0.16% Agar and 1% Glycine (ATCC Medium 2161)
Composition per liter:
Agar ..................................................................17.5g Pancreatic digest of casein................................10.0g Peptic digest of animal tissue............................10.0g NaCl ....................................................................5.0g Yeast extract........................................................2.0g Glucose ...............................................................1.0g NaHSO3 ..............................................................0.1g
lobacter species.
Composition per liter: Pancreatic digest of casein................................10.0g Peptic digest of animal tissue ...........................10.0g Glycine..............................................................10.0g NaCl....................................................................5.0g Yeast extract........................................................2.0g
88
Brucella Albimi Broth with Formate and Fumarate
Agar ....................................................................1.6g Glucose ...............................................................1.0g NaHSO3 ..............................................................0.1g Horse blood, defibrinated ........................... 100.0mL pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Add components, except horse blood, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Heat gently with frequent mixing. Boil for 1 min. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°– 50°C. Aseptically add 100.0mL of sterile defibrinated horse blood. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation and maintenance of Campylobacter species.
Brucella Albimi Broth with Formate and Fumarate Composition per 1050.0mL: Pancreatic digest of casein................................10.0g Peptic digest of animal tissue............................10.0g NaCl ....................................................................5.0g Yeast extract........................................................2.0g Glucose ...............................................................1.0g NaHSO3 ..............................................................0.1g Horse blood, defibrinated ........................... 100.0mL Formate-fumarate solution............................ 50.0mL pH 7.0 ± 0.2 at 25°C
Formate-Fumarate Solution: Composition per 100.0mL: Sodium formate...................................................6.0g Fumaric acid .......................................................6.0g
Preparation of Formate-Fumarate Solution: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Adjust pH to 7.0. Filter sterilize.
Preparation of Medium: Add components, except formate-fumarate solution and horse blood, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Heat gently with frequent mixing. Boil for 1 min. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Add 100.0mL of sterile defibrinated horse blood. Mix gently and aseptically distribute into sterile tubes in 5.0mL volumes. Aseptically add 0.25mL of formatefumarate solution to each tube containing 5.0mL of medium immediately prior to inoculation.
Use: For the cultivation and maintenance of Campylobacter mucosalis.
Brucella Albimi Broth with Sheep Blood Composition per liter: Pancreatic digest of casein................................10.0g Peptic digest of animal tissue ...........................10.0g NaCl....................................................................5.0g Yeast extract........................................................2.0g Glucose ...............................................................1.0g NaHSO3 ..............................................................0.1g Sheep blood, defibrinated ........................... 100.0mL pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Add components, except sheep blood, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Heat gently with frequent mixing. Boil for 1 min. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°– 50°C. Aseptically add 100.0mL of sterile defibrinated sheep blood. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation and maintenance of Helicobacter nemestrinae and Helicobacter pylori.
Brucella Albimi Medium, Semisolid Composition per liter: Pancreatic digest of casein................................10.0g Peptic digest of animal tissue ...........................10.0g Glycine..............................................................10.0g NaCl....................................................................8.5g Yeast extract........................................................2.0g Agar ....................................................................1.6g Glucose ...............................................................1.0g L-Cysteine·HCl·H2O............................................0.2g NaHSO3 ..............................................................0.1g pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.0. Gently heat and bring to boiling. Distribute into tubes in 10.0mL volumes. Autoclave for 15 min at 15 psi pressure– 121°C. Allow tubes to cool in an upright position.
Use: For the cultivation and identification of Campylobacter species.
Brucella Anaerobic Blood Agar Composition per liter: Vitamin K1 ........................................................0.01g Anaerobic agar base.................................. 1000.0mL Sheep blood, sterile, defibrinated ................. 50.0mL
Anaerobic Agar Base Composition per liter: Pancreatic digest of casein................................17.5g Agar ..................................................................15.0g
Brucella Broth Glucose .............................................................10.0g Papaic digest of soybean meal ............................2.5g NaCl ....................................................................2.5g Sodium thioglycolate ..........................................2.0g Sodium formaldehyde sulfoxylate ......................1.0g L-Cystine·HCl·H2O .............................................0.4g Methylene Blue...............................................0.002g pH 7.0 ± 0.2 at 25°C
Preparation of Anaerobic Agar Base: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Preparation of Medium: To 950.0mL of cooled, sterile anaerobic agar base, aseptically add 10.0mg of vitamin K1 and 50.0mL of sterile, defibrinated sheep blood.
Use: For the isolation of anaerobes.
Brucella Blood Agar with Hemin and Vitamin K1
Composition per liter:
Agar ..................................................................15.0g Pancreatic digest of casein................................10.0g Peptic digest of animal tissue............................10.0g NaCl ....................................................................5.0g Yeast extract........................................................2.0g Glucose ...............................................................1.0g NaHSO3 ..............................................................0.1g Vitamin K1 solution......................................... 1.0mL Hemin solution................................................ 1.0mL Sheep blood, defibrinated ............................. 50.0mL
Source: This medium is available as a prepared medium from BD Diagnostic Systems.
Vitamin K1 Solution: Composition per 100.0mL:
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Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C. Aseptically add 1.0mL of sterile vitamin K1 solution and 50.0mL of sterile defibrinated sheep blood. Mix gently and pour into sterile Petri dishes.
Use: For the isolation and cultivation of anaerobic microorganisms from clinical specimens. After growth on agar plates, colonies should be examined under a dissecting microscope under long-wave UV light. Members of the pigmented Bacteroides group appear as red/orange fluorescent colonies.
Brucella Blood Culture Broth Composition per liter: Sucrose............................................................100.0g Hemin .................................................................0.5g Sodium polyanetholsulfonate (SPS) .................0.25g Brucella broth base ................................... 1000.0mL Vitamin K1 solution ........................................ 1.0mL pH 7.0 ± 0.2 at 25°C
Brucella Broth Base: Composition per liter: Pancreatic digest of casein................................10.0g Peptic digest of animal tissue ...........................10.0g NaCl....................................................................5.0g Yeast extract........................................................2.0g Glucose ...............................................................1.0g NaHSO3 ..............................................................0.1g
Preparation of Brucella Broth Base: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly.
Vitamin K1 Solution: Composition per 100.0mL: Vitamin K1 ........................................................1.09g Ethanol, absolute........................................... 99.0mL
Preparation of Vitamin K1 Solution: Add vita-
Vitamin K1 ..........................................................1.0g Ethanol .......................................................... 99.0mL
min K1 to 99.0mL of absolute ethanol. Store in the dark at 4°C.
Preparation of Vitamin K1 Solution: Add vita-
Preparation of Medium: Add components, ex-
Hemin Solution: Composition per 100.0mL:
cept vitamin K1 solution, to prepared Brucella broth base. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 1.0mL of vitamin K1 solution. Distribute into sterile tubes or flasks.
min K1 to 99.0mL of absolute ethanol. Mix thoroughly. Filter sterilize.
Hemin..................................................................1.0g NaOH (1N solution)...................................... 20.0mL
Use: For the isolation and cultivation of microorgan-
Preparation of Hemin Solution: Add hemin to
isms from blood. Especially useful for the cultivation of anaerobes.
20.0mL of 1N NaOH solution. Mix thoroughly. Bring volume to 100.0mL with distilled/deionized water.
Brucella Broth (Brucella Albimi Broth)
Preparation of Medium: Add components, ex-
Composition per liter:
cept vitamin K1 solution and sheep blood, to distilled/deionized water and bring volume to 949.0mL.
Pancreatic digest of casein................................10.0g Peptic digest of animal tissue ...........................10.0g
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Brucella Broth with Additives
NaCl ....................................................................5.0g Yeast extract........................................................2.0g Glucose ...............................................................1.0g NaHSO3 ..............................................................0.1g Horse blood, defibrinated ............................. 50.0mL pH 7.0 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components, except horse blood, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Heat gently with frequent mixing. Boil for 1 min. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°– 50°C. Aseptically add 50.0mL of sterile horse blood. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation and maintenance of Campylobacter coli, Campylobacter fecalis, and Brucella species. Also used for the isolation and cultivation of a wide variety of fastidious and nonfastidious microorganisms.
Brucella Broth with Additives (ATCC Medium 489) Composition per liter: Pancreatic digest of casein................................10.0g Peptic digest of animal tissue............................10.0g NaCl ....................................................................3.5g Yeast extract........................................................2.0g Glucose ...............................................................1.0g NaHSO3 ..............................................................0.1g Horse serum, inactivated............................. 100.0mL Fresh yeast extract solution........................... 50.0mL pH 7.0 ± 0.2 at 25°C
Fresh Yeast Extract Solution: Composition per 100.0mL: Baker’s yeast, live, pressed, starch-free............25.0g
Preparation of Fresh Yeast Extract Solution: Add the live Baker’s yeast to 100.0mL of distilled/ deionized water. Autoclave for 90 min at 15 psi pressure–121°C. Allow to stand. Remove supernatant solution. Adjust pH to 6.6–6.8. Preparation of Medium: Add components, except horse serum and fresh yeast extract solution, to distilled/deionized water and bring volume to 850.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C. Aseptically add 100.0mL of sterile horse serum and 50.0mL of sterile fresh yeast extract solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation of Corynebacterium species.
Brucella Broth with Additives (ATCC Medium 490) Composition per liter: NaCl..................................................................30.0g Pancreatic digest of casein................................10.0g Peptic digest of animal tissue ...........................10.0g Yeast extract........................................................2.0g Glucose ...............................................................1.0g NaHSO3 ..............................................................0.1g Horse serum, inactivated ............................ 100.0mL Fresh yeast extract solution .......................... 50.0mL pH 7.0 ± 0.2 at 25°C
Fresh Yeast Extract Solution: Composition per 100.0mL: Baker’s yeast, live, pressed, starch-free............25.0g
Preparation of Fresh Yeast Extract Solution: Add the live Baker’s yeast to 100.0mL of distilled/ deionized water. Autoclave for 90 min at 15 psi pressure–121°C. Allow to stand. Remove supernatant solution. Adjust pH to 6.6–6.8. Preparation of Medium: Add components, except horse serum and fresh yeast extract solution, to distilled/deionized water and bring volume to 850.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C. Aseptically add 100.0mL of horse serum and 50.0mL of sterile fresh yeast extract solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation of salt-tolerant Corynebacterium species.
Brucella Broth with 0.16% Agar (ATCC Medium 1116) Composition per liter: Pancreatic digest of casein................................10.0g Peptic digest of animal tissue ...........................10.0g NaCl....................................................................5.0g Yeast extract........................................................2.0g Agar ....................................................................1.6g Glucose ...............................................................1.0g NaHSO3 ..............................................................0.1g Horse blood, defibrinated ............................. 50.0mL pH 7.0 ± 0.2 at 25°C
Source: This medium without agar is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components, except horse blood, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Heat gently with frequent mixing. Boil for 1 min. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°– 50°C. Aseptically add 50.0mL of sterile horse blood.
Brucella FBP Broth Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation and maintenance of Campylobacter fetus subsp. Fetus and Campylobacter jejuni subsp. Jejuni.
Brucella Broth Base Campylobacter Medium Composition per liter: Cycloheximide (actidione).............................50.0mg Sodium cephazolin.........................................15.0mg Novobiocin.......................................................5.0mg Bacitracin .....................................................25,000U Colistin sulfate .............................................10,000U Brucella broth base ..................................... 900.0mL Horse blood, defibrinated ........................... 100.0mL pH 7.0 ± 0.2 at 25°C
Brucella Broth Base: Composition per liter: Pancreatic digest of casein................................10.0g Peptic digest of animal tissue............................10.0g NaCl ....................................................................5.0g Yeast extract........................................................2.0g Glucose ...............................................................1.0g NaHSO3 ..............................................................0.1g
Preparation of Brucella Broth Base: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly.
Optional Supplement: Composition per 10.0mL: Sodium pyruvate ...............................................0.25g NaHSO3 ............................................................0.25g FeSO4·7H2O......................................................0.25g
Preparation of Optional Supplement: Add components to distilled/deionized water and bring volume to 10.0mL. Filter sterilize. Preparation of Medium: Add components, except horse blood, to 900.0mL of prepared Brucella broth base. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 100.0mL of sterile, defibrinated horse blood. Addition of 10.0mL of optional supplement will improve growth. Mix thoroughly. Pour into sterile Petri dishes.
Use: For the selective isolation and cultivation of Campylobacter jejuni from fecal specimens or rectal swabs. Addition of the optional supplement improves growth.
Brucella Broth, Modified Composition per liter: Pancreatic digest of casein................................10.0g
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Peptic digest of animal tissue ...........................10.0g NaCl....................................................................5.0g MgSO4·7H2O ....................................................2.46g Yeast extract........................................................2.0g CaCl2 ...................................................................1.1g Glucose ...............................................................1.0g NaHSO3 ..............................................................0.1g Horse blood, defibrinated ........................... 100.0mL pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Add components, except horse blood, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile horse blood. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation and maintenance of Campylobacter coli and Campylobacter fecalis.
Brucella FBP Agar Composition per liter: Agar ..................................................................15.0g Pancreatic digest of casein................................10.0g Peptic digest of animal tissue ...........................10.0g NaCl....................................................................5.0g Yeast extract........................................................2.0g Glucose ...............................................................1.0g NaHSO3 ..............................................................0.1g FBP solution ................................................. 30.0mL pH 7.0 ± 0.2 at 25°C
FBP Solution: Composition per 30.0mL: FeSO4 ................................................................0.25g NaHSO3 ............................................................0.25g Sodium pyruvate...............................................0.25g
Preparation of FBP Solution: Add components to distilled/deionized water and bring volume to 30.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except FBP solution, to distilled/deionized water and bring volume to 970.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 30.0mL of sterile FBP solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation of Brucella species.
Brucella FBP Broth Composition per liter: Pancreatic digest of casein................................10.0g Peptic digest of animal tissue ...........................10.0g
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Brucella Medium Base
NaCl ....................................................................5.0g Yeast extract........................................................2.0g Glucose ...............................................................1.0g NaHSO3 ..............................................................0.1g FBP solution ................................................. 30.0mL pH 7.0 ± 0.2 at 25°C
bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, ex-
FeSO4 ................................................................0.25g Sodium metabisulfite, anhydrous .....................0.25g Sodium pyruvate, anhydrous ............................0.25g
cept horse serum and VCNF antibiotic solution, to distilled/deionized water and bring volume to 890.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C. Aseptically add 100.0mL of sterile horse serum and 10.0mL of VCNF antibiotic solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Preparation of FBP Solution: Add components
Use: For the selective isolation, cultivation, and
FBP Solution: Composition per 30.0mL:
to distilled/deionized water and bring volume to 30.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except FBP solution, to distilled/deionized water and bring volume to 970.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 30.0mL of sterile FBP solution. Mix thoroughly. Aseptically distribute into sterile tubes.
Use: For the cultivation of Brucella species.
Brucella Medium Base Composition per liter:
maintenance of Brucella species.
Brucella Selective Medium Composition per liter: Beef heart, infusion from................................500.0g Agar ..................................................................15.0g Tryptose ............................................................10.0g NaCl....................................................................5.0g Glucose ...............................................................2.5g Gelatin.................................................................1.0g Sheep blood ................................................ 100.0mL Antibiotic solution ........................................ 10.0mL pH 7.4 ± 0.2 at 25°C
Agar ..................................................................15.0g Glucose .............................................................10.0g Peptone..............................................................10.0g Beef extract .........................................................5.0g NaCl ....................................................................5.0g pH 7.5 ± 0.2 at 25°C
Antibiotic Solution: Composition per 10.0mL:
Preparation: Add components to distilled/deionized
Preparation of Antibiotic Solution: Add com-
water and bring volume to 1.0L. Mix thoroughly. Heat gently and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the isolation of Campylobacter species.
Brucella Medium, Selective Composition per liter: Agar ..................................................................15.0g Pancreatic digest of casein................................10.0g Peptic digest of animal tissue............................10.0g NaCl ....................................................................5.0g Yeast extract........................................................2.0g Glucose ...............................................................1.0g NaHSO3 ..............................................................0.1g Horse serum ................................................ 100.0mL VCNF antibiotic solution.............................. 10.0mL pH 7.0 ± 0.2 at 25°C
Preparation of VCNF Antibiotic Solution: Add components to distilled/deionized water and
Cycloheximide....................................................1.0g Bacitracin................................................... 250,000U Circulin ...................................................... 250,000U Polymyxin B .............................................. 100,000U ponents to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except sheep blood and antibiotic solution, to distilled/ deionized water and bring volume to 890.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 100.0mL of sterile sheep blood and 10.0mL of sterile antibiotic solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the selective isolation and cultivation of Brucella species.
Brucella Semisolid Medium with Cysteine Composition per liter: Peptamin ...........................................................10.0g Pancreatic digest of casein................................10.0g Glycine..............................................................10.0g
Brucella Semisolid Medium with Nitrate NaCl ....................................................................5.0g Yeast extract........................................................2.0g Agar ....................................................................1.8g Glucose ...............................................................1.0g L-Cysteine·HCl·H2O ...........................................0.2g NaHSO3 ..............................................................0.1g Sodium citrate .....................................................0.1g Neutral Red solution ..................................... 10.0mL pH 7.0 ± 0.2 at 25°C
Neutral Red Solution: Composition per 100.0mL: Neutral Red .........................................................0.2g Ethanol .......................................................... 10.0mL
Preparation of Neutral Red Solution: Add Neutral Red to 10.0mL of ethanol. Bring volume to 100.0mL.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes in 10.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation and differentiation of Campylobacter species based on H2S production from cysteine.
Brucella Semisolid Medium with Glycine Composition per liter: Peptamine..........................................................10.0g Pancreatic digest of casein................................10.0g Glycine..............................................................10.0g NaCl ....................................................................5.0g Yeast extract........................................................2.0g Agar ....................................................................1.8g Glucose ...............................................................1.0g NaHSO3 ..............................................................0.1g Sodium citrate .....................................................0.1g Neutral Red solution ..................................... 10.0mL pH 7.0 ± 0.2 at 25°C
Neutral Red Solution: Composition per 100.0mL: Neutral Red .........................................................0.2g Ethanol .......................................................... 10.0mL
Preparation of Neutral Red Solution: Add Neutral Red to 10.0mL of ethanol. Bring volume to 100.0mL.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes in 10.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C.
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Use: For the cultivation and differentiation of Campylobacter species based on glycine utilization.
Brucella Semisolid Medium with NaCl Composition per liter: NaCl..................................................................35.0g Peptamin ...........................................................10.0g Pancreatic digest of casein................................10.0g Yeast extract........................................................2.0g Agar ....................................................................1.8g Glucose ...............................................................1.0g NaHSO3 ..............................................................0.1g Sodium citrate.....................................................0.1g Neutral Red solution ..................................... 10.0mL pH 7.0 ± 0.2 at 25°C
Neutral Red Solution: Composition per 100.0mL: Neutral Red.........................................................0.2g Ethanol.......................................................... 10.0mL
Preparation of Neutral Red Solution: Add Neutral Red to 10.0mL of ethanol. Bring volume to 100.0mL.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes in 10.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation and differentiation of Campylobacter species based on glycine utilization.
Brucella Semisolid Medium with Nitrate Composition per liter: Peptamin ...........................................................10.0g Pancreatic digest of casein................................10.0g Glycine..............................................................10.0g KNO3 ................................................................10.0g NaCl....................................................................5.0g Yeast extract........................................................2.0g Agar ....................................................................1.8g Glucose ...............................................................1.0g NaHSO3 ..............................................................0.1g Sodium citrate.....................................................0.1g pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes in 10.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation and differentiation of Campylobacter species based on nitrate reduction.
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BSK Medium
BSK Medium Composition per 1260.0mL: Bovine albumin fraction V ...............................50.0g HEPES (N-[2-Hydroxyethyl]piperazine-N´-2ethanesulfonic acid) buffer .......................6.0g Neopeptone .........................................................5.0g Glucose ...............................................................5.0g NaHCO3 ..............................................................2.2g Sodium pyruvate .................................................0.8g Sodium citrate .....................................................0.7g N-Acetylglucosamine..........................................0.4g Gelatin solution........................................... 200.0mL CMRL 1066, without glutamine, without bicarbonate, 10X ................. 100.0mL Rabbit serum ................................................. 72.0mL pH 7.6-7.65 at 25°C
Gelatin Solution: Composition per 200.0mL: Gelatin...............................................................14.0g
Preparation of Gelatin Solution: Add gelatin to distilled/deionized water and bring volume to 200.0mL. Heat gently to boiling. Mix thoroughly. Filter sterilize. CMRL 1066 Medium without Glutamine, without Bicarbonate, 10X: Composition per liter: NaCl ....................................................................6.8g D-Glucose ............................................................1.0g KCl......................................................................0.4g L-Cysteine·HCl·H2O..........................................0.26g CaCl2, anhydrous ................................................0.2g MgSO4·7H2O ......................................................0.2g NaH2PO4·H2O...................................................0.14g Sodium acetate·3H2O......................................0.083g L-Glutamic acid ...............................................0.075g L-Arginine·HCl..................................................0.07g L-Lysine·HCl .....................................................0.07g L-Leucine...........................................................0.06g Glycine..............................................................0.05g Ascorbic acid ....................................................0.05g L-Proline ............................................................0.04g L-Tyrosine..........................................................0.04g L-Aspartic acid ..................................................0.03g L-Threonine .......................................................0.03g L-Alanine.........................................................0.025g L-Phenylalanine...............................................0.025g L-Serine ...........................................................0.025g L-Valine ...........................................................0.025g L-Cystine ...........................................................0.02g L-Histidine·HCl·H2O .........................................0.02g L-Isoleucine .......................................................0.02g Phenol Red........................................................0.02g L-Methionine ...................................................0.015g Deoxyadenosine................................................0.01g
Deoxycytidine...................................................0.01g Deoxyguanosine ...............................................0.01g Glutathione, reduced.........................................0.01g Thymidine.........................................................0.01g Hydroxy-L-proline ............................................0.01g L-Tryptophan.....................................................0.01g Nicotinamide adenine dinucleotide .................7.0mg Tween 80..........................................................5.0mg Sodium glucoronate·H2O.................................4.2mg Coenzyme A ....................................................2.5mg Cocarboxylase..................................................1.0mg Flavin adenine dinucleotide.............................1.0mg Nicotinamide adenine dinucleotide phosphate..............................1.0mg Uridine triphosphate ........................................1.0mg Choline chloride...............................................0.5mg Cholesterol.......................................................0.2mg 5-Methyldeoxycytidine....................................0.1mg Inositol ...........................................................0.05mg p-Aminobenzoic acid.....................................0.05mg Niacin...........................................................0.025mg Niacinamide.................................................0.025mg Pyridoxine....................................................0.025mg Pyridoxal·HCl ..............................................0.025mg Biotin .............................................................0.01mg D-Calcium pantothenate .................................0.01mg Folic acid .......................................................0.01mg Riboflavin ......................................................0.01mg Thiamine·HCl ................................................0.01mg pH 7.2 ± 0.2 at 25°C
Preparation of CMRL 1066 Medium without Glutamine, without Bicarbonate, 10X: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.2. Filter sterilize.
Preparation of Medium: Add components, except gelatin solution and rabbit serum, to 628.0mL of glass-distilled water. Mix thoroughly. Adjust pH to 7.6–7.65. Add 200.0mL of 7% aqueous gelatin solution. Filter sterilize entire medium. Aseptically add 72.0mL of sterile rabbit serum.
Use: For the cultivation of a wide variety of microorganisms in a chemically defined medium. For the cultivation of Borrelia and Spirochaeta species.
BSK Medium, Modified Composition per 1264.0mL: Bovine serum albumin, fraction V....................50.0g HEPES (N-[2-Hydroxymethyl]piperazine-N´ [ethane sulfonate]) buffer .............................6.0g Neopeptone .........................................................5.0g Glucose ...............................................................5.0g Yeastolate..........................................................2.54g NaHCO3 ..............................................................2.2g
BSK Medium, Revised Sodium pyruvate .................................................0.8g Sodium citrate .....................................................0.7g MgSO4·7H2O......................................................0.6g N-Acetylglucosamine..........................................0.4g CaCl2·2H2O ......................................................0.07g CMRL 1066, 10X without glutamine or NaHCO3 ............. 100.0mL Rabbit serum, heat inactivated...................... 64.0mL pH 7.5 ± 0.2 at 25°C
CMRL 1066, 10X without Glutamine or NaHCO3: Composition per liter: NaCl ....................................................................6.8g D-Glucose ............................................................1.0g KCl......................................................................0.4g L-Cysteine·HCl·H2O..........................................0.26g CaCl2, anhydrous ................................................0.2g MgSO4·7H2O ......................................................0.2g NaH2PO4·H2O...................................................0.14g Sodium acetate·3H2O......................................0.083g L-Glutamic acid ...............................................0.075g L-Arginine·HCl................................................0.070g L-Lysine·HCl ...................................................0.070g L-Leucine.........................................................0.060g Glycine............................................................0.050g Ascorbic acid ..................................................0.050g L-Proline ..........................................................0.040g L-Tyrosine........................................................0.040g L-Aspartic acid ................................................0.030g L-Threonine .....................................................0.030g L-Alanine.........................................................0.025g L-Phenylalanine...............................................0.025g L-Serine ...........................................................0.025g L-Valine ...........................................................0.025g L-Cystine .........................................................0.020g L-Histidine·HCl·H2O .......................................0.020g L-Isoleucine .....................................................0.020g Phenol Red......................................................0.020g L-Methionine ...................................................0.015g Deoxyadenosine..............................................0.010g Deoxycytidine.................................................0.010g Deoxyguanosine..............................................0.010g Glutathione, reduced.......................................0.010g Thymidine.......................................................0.010g Hydroxy-L-proline...........................................0.010g L-Tryptophan ...................................................0.010g Nicotinamide adenine dinucleotide .................7.0mg Tween 80..........................................................5.0mg Sodium glucoronate·H2O.................................4.2mg Coenzyme A ....................................................2.5mg Cocarboxylase..................................................1.0mg Flavin adenine dinucleotide .............................1.0mg Nicotinamide adenine dinucleotide phosphate ..............................1.0mg Uridine triphosphate ........................................1.0mg
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Choline chloride.............................................0.50mg Cholesterol.....................................................0.20mg 5-Methyldeoxycytidine..................................0.10mg Inositol ...........................................................0.05mg p-Aminobenzoic acid.....................................0.05mg Niacin...........................................................0.025mg Niacinamide.................................................0.025mg Pyridoxine....................................................0.025mg Pyridoxal·HCl ..............................................0.025mg Biotin .............................................................0.01mg D-Calcium pantothenate .................................0.01mg Folic acid .......................................................0.01mg Riboflavin ......................................................0.01mg Thiamine·HCl ................................................0.01mg
Preparation of CMRL 1066, 10X Without Glutamine or NaHCO3: Add components to dis-
tilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.2. Filter sterilize.
Preparation of Medium: Add components, except CMRL 1066, 10X without glutamine or NaHCO3 and rabbit serum, to distilled/deionized water and bring volume to 1100.0mL. Mix thoroughly. Adjust pH to 7.5 with NaOH. Filter sterilize. Aseptically add 100.0mL of sterile CMRL 1066, 10X without glutamine or NaHCO3 and 64.0mL of sterile rabbit serum. Mix thoroughly. Aseptically distribute 10.0mL volumes into sterile 16 × 125.0mm test tubes.
Use: For the cultivation of Borrellia afzelii, Borrelia burgdorferi, and Borrelia gorinii.
BSK Medium, Revised Composition per 1164.0mL: Bovine serum albumin fraction V.....................50.0g HEPES (N-[2-Hydroxyethyl]piperazine-N´-2ethanesulfonic acid) buffer.......................6.0g Neopeptone .........................................................5.0g Glucose ...............................................................5.0g TC-Yeastolate ...................................................2.54g NaHCO3 ..............................................................2.2g Sodium pyruvate.................................................0.8g Sodium citrate.....................................................0.7g N-Acetyl glucosamine ........................................0.4g CMRL 1066, without glutamine, without bicarbonate, 10X ................. 100.0mL Rabbit serum................................................. 64.0mL pH 7.6–7.65 at 25°C
CMRL 1066 Medium without Glutamine, without Bicarbonate, 10X: Composition per liter: NaCl....................................................................6.8g D-Glucose ............................................................1.0g KCl......................................................................0.4g
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BTB Lactose Agar
L-Cysteine·HCl·H2O..........................................0.26g
CaCl2, anhydrous ................................................0.2g MgSO4·7H2O ......................................................0.2g NaH2PO4·H2O...................................................0.14g Sodium acetate·3H2O......................................0.083g L-Glutamic acid ...............................................0.075g L-Arginine·HCl................................................0.070g L-Lysine·HCl ...................................................0.070g L-Leucine.........................................................0.060g Glycine............................................................0.050g Ascorbic acid ..................................................0.050g L-Proline ..........................................................0.040g L-Tyrosine........................................................0.040g L-Aspartic acid ................................................0.030g L-Threonine .....................................................0.030g L-Alanine.........................................................0.025g L-Phenylalanine...............................................0.025g L-Serine ...........................................................0.025g L-Valine ...........................................................0.025g L-Cystine .........................................................0.020g L-Histidine·HCl·H2O .......................................0.020g L-Isoleucine .....................................................0.020g Phenol Red......................................................0.020g L-Methionine ...................................................0.015g Deoxyadenosine..............................................0.010g Deoxycytidine.................................................0.010g Deoxyguanosine..............................................0.010g Glutathione, reduced.......................................0.010g Thymidine.......................................................0.010g Hydroxy-L-proline...........................................0.010g L-Tryptophan ...................................................0.010g Nicotinamide adenine dinucleotide .................7.0mg Tween 80..........................................................5.0mg Sodium glucoronate·H2O.................................4.2mg Coenzyme A ....................................................2.5mg Cocarboxylase..................................................1.0mg Flavin adenine dinucleotide .............................1.0mg Nicotinamide adenine dinucleotide phosphate ..............................1.0mg Uridine triphosphate ........................................1.0mg Choline chloride.............................................0.50mg Cholesterol .....................................................0.20mg 5-Methyldeoxycytidine..................................0.10mg Inositol ...........................................................0.05mg p-Aminobenzoic acid.....................................0.05mg Niacin...........................................................0.025mg Niacinamide .................................................0.025mg Pyridoxine....................................................0.025mg Pyridoxal·HCl ..............................................0.025mg Biotin .............................................................0.01mg Calcium DL-pantothenate...............................0.01mg Folic acid........................................................0.01mg Riboflavin ......................................................0.01mg Thiamine·HCl ................................................0.01mg pH 7.2 ± 0.2 at 25°C
Preparation of CMRL 1066 Medium without Glutamine, without Bicarbonate, 10X: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.2. Filter sterilize.
Preparation of Medium: Add components, except rabbit serum and CMRL 1066, to 1.0L of glassdistilled/deionized water. Mix thoroughly. Adjust pH to 7.5 with NaOH. Filter sterilize. Aseptically add 100.0mL of sterile CMRL 1066 and 64.0mL of sterile rabbit serum. Adjust final pH to 7.5–7.6. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation of Borrelia burgdorferi, Borrelia afzelii, Borrelia garinii, Borrelia anserina, and Borrelia japonica.
BTB Lactose Agar (Bromthymol Blue Lactose Agar) Composition per liter: Agar ..................................................................15.0g Lactose..............................................................10.0g Proteose peptone.................................................5.0g Beef extract.........................................................3.0g Bromthymol Blue .............................................0.17g pH 8.7–7.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Heat gently with frequent mixing. Bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes if desired.
Use: For the isolation and cultivation of pathogenic staphylococci.
BTB Teepol® Agar Composition per liter: NaCl..................................................................20.0g Agar ..................................................................15.0g Peptone .............................................................10.0g Sucrose..............................................................10.0g Beef extract.........................................................5.0g Bromthymol Blue .............................................0.08g Teepol ............................................................. 2.0mL pH 7.8 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Teepol may be substituted by 0.1mL of Tergitol™ 7. Mix thoroughly. Gently heat and bring to boiling. Adjust pH to 7.8. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes.
Use: For the isolation and cultivation of Vibrio anguillarum.
Buffered Enrichment Broth
BTU Medium Composition per liter:
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Antibiotic Solution: Composition per 10.0mL:
Ground meat, fat free ......................................500.0g Pancreatic digest of casein................................30.0g K2HPO4 ...............................................................5.0g Yeast extract........................................................5.0g L-Cysteine·HCl ...................................................0.5g Resazurin .........................................................1.0mg NaOH (1N solution)...................................... 25.0mL Formate-fumarate solution............................ 4.26mL pH 7.0 ± 0.2 at 25°C
Vancomycin .....................................................1.0mg Polymyxin B ................................................ 50,000U
Formate-Fumarate Solution: Composition per 100.0mL:
Preparation of L-Cysteine·HCl·H2O Solution:
Sodium formate...................................................6.0g Sodium fumarate.................................................6.0g
Preparation of Formate-Fumarate Solution: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize. Preparation of Medium: Use lean beef or horse meat. Remove fat and connective tissue. Grind finely. Add ground meat and 25.0mL of NaOH solution to distilled/deionized water and bring volume to 1025.0mL. Gently heat and bring to boiling. Continue boiling for 15 min without stirring. Cool to room temperature. Remove fat from surface. Filter and retain both meat particles and filtrate. Adjust volume of filtrate to 1.0L with distilled/deionized water. Add casitone, K2HPO4, yeast extract, and resazurin. Gently heat and bring to boiling. Boil for 1–2 min. Add L-cysteine·HCl. Mix thoroughly. Distribute 7.0mL into tubes that contain meat particles (1 part meat particles to 5 parts fluid). Autoclave for 30 min at 15 psi pressure–121°C. Prior to inoculation, add 30.0µL of formate-fumarate solution for each milliliter of medium in the tubes.
Use: For the cultivation of Bacteroides ureolyticus.
Buffered Charcoal Yeast Extract Differential Agar (DIFF/BCYE) Composition per 1014.0mL: Agar ..................................................................17.0g ACES (2-[(2-Amino-2-oxoethyl)amino]-ethane sulfonic acid) buffer ...........10.0g Yeast extract......................................................10.0g Charcoal, activated..............................................1.5g Fe4(P2O7)3·9H2O...............................................0.25g Bromcresol Purple ............................................0.01g Bromthymol Blue .............................................0.01g Antibiotic solution ........................................ 10.0mL L-Cysteine·HCl·H2O solution ......................... 4.0mL pH 6.9 ± 0.2 at 25°C
Preparation of Antibiotic Solution: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. L-Cysteine·HCl·H2O
Solution: Composition per 10.0mL: L-Cysteine·HCl·H2O............................................1.0g
Add L-cysteine·HCl·H2O to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except L-cysteine·HCl·H2O solution and antibiotic solution, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust medium to pH 6.9 with 1N KOH. Heat gently and bring to boil for 1 min. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Add 4.0mL of sterile L-cysteine·HCl·H2O solution and 10.0mL of sterile antibiotic solution. Mix thoroughly. Pour into sterile Petri dishes with constant agitation to keep charcoal in suspension.
Use: For the isolation, cultivation, and maintenance of Legionella pneumophila and other Legionella species from environmental and clinical specimens. For the selective recovery of Legionella pneumophila while reducing contaminating microorganisms from environmental water samples.
Buffered Enrichment Broth Composition per liter: Na2HPO4 .............................................................9.6g KH2PO4.............................................................1.35g Pyruvic acid solution .................................... 11.1mL Nalidixic acid solution.................................... 8.0mL Cyclohiximide solution................................... 5.0mL Acriflavin solution .......................................... 2.0mL pH 7.3 ± 0.1 at 25°C
Nalidixic Acid Solution: Composition per 10.0mL: Nalidixic acid, sodium salt ...............................0.05g
Preparation of Nalidixic Acid Solution: Add nalidixic acid to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. Acriflavin Solution: Composition per 10.0mL: Acriflavin·HCl ..................................................0.05g
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Buffered Peptone Water
Preparation of Acriflavin Solution: Add acri-
Pyruvate Solution: Composition per 20.0mL:
Sodium pyruvate.................................................7.0g Peptone ...............................................................5.0g KH2PO4...............................................................4.4g Yeast Extract .......................................................4.0g Bile salts..............................................................1.5g Na2HPO4 .............................................................1.4g (NH4)2SO4 ..........................................................1.0g MgSO4 ................................................................0.2g Phenol Red........................................................0.02g Fe(NH4)2(SO4)2·6H2O ......................................0.01g Crystal Violet ..................................................0.001g Selective supplement solution ...................... 10.0mL pH 6.2 ± 0.2 at 25°C
Na-pyruvate ........................................................2.0g
Source: This medium is available as a premixed
Preparation of Pyruvate Solution: Add Na-
powder from Oxoid Unipath.
pyruvate to distilled/deionized water and bring volume to 20.0mL. Mix thoroughly. Filter sterilize.
Selective Supplement Solution: Composition per 10.0mL:
Preparation of Medium: Add components, ex-
Polymyxin B .............................................150,000IU Ticarcillin.....................................................100.0mg Gentamicin.......................................................5.0mg
flavin·HCl to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Cycloheximide Solution: Composition per 10.0mL: Cycloheximide ....................................................0.1g Ethanol, 40%................................................. 10.0mL
Preparation of Cycloheximide Solution: Add cycloheximide to 40% ethanol and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
cept pyruvate solution, nalidixic acid solution, acriflavin solution, and cycloheximide solution, to distilled/deionized water and bring volume to 973.9.0L. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 25°C. Aseptically add 11.1mL sterile pyruvate solution. Mix thoroughly. Aseptically add 8.0mL sterile nalidixic acid solution, 5.0mL sterile cycloheximide solution, and 2.0mL sterile acriflavin solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation of of Listeria spp.
Buffered Peptone Water Composition per liter: Pancreatic digest of gelatin ...............................10.0g NaCl ....................................................................5.0g Na2HPO4 .............................................................3.5g KH2PO4 ...............................................................1.5g pH 7.2 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems and Oxoid Unipath. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: Used as a preenrichment medium for the isolation of Salmonella, especially injured microorganisms.
Burkholderia cepacia Agar Composition per liter: Agar ..................................................................12.0g
Preparation of Selective Supplement Solution: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except selective supplement solution, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 50°C. Aseptially add 10.0mL selective supplement solution. Mix thoroughly. Pour into sterile Petri dishes.
Use: For the selective isolation of Burkholderia cepacia from the respiratory secretions of patients with cystic fibrosis and for routine testing of nonsterile inorganic salt solutions containing preservative.Slow growing B. cepacia can be missed on conventional media such as blood or MacConkey Agar due to overgrowth caused by other faster growing organisms found in the respiratory tract of CF patients such as mucoid Klebsiella species, Pseudomonas aeruginosa, and Staphylococcus species. This may lead to the infection being missed or wrongly diagnosed.
BYE Agar Composition per liter: Pancreatic digest of casein................................16.0g Agar ..................................................................13.5g Brain heart, solids from infusion ........................8.0g Peptic digest of animal tissue .............................5.0g NaCl....................................................................5.0g Na2HPO4 .............................................................2.5g Glucose ...............................................................2.0g
Caffeine Medium Yeast extract........................................................2.0g Blood, human or animal, sterile.................. 150.0mL pH 7.8–8.0 ± 0.2 at 25°C
Preparation of Medium: Add components, except blood, to distilled/deionized water and bring volume to 850.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 150.0mL of sterile blood. Outdated, citrated, or heparinized blood (blood from a blood bank is acceptable). Pour into sterile Petri dishes.
Use: For the isolation and cultivation of Mycoplasma species and L-forms of bacteria. For the detection of Mycoplasma species in tissue culture and cell lines.
BYEB (Buffered Yeast Extract Broth) Composition per liter: ACES buffer (2-[(2-Amino-2-oxoethyl)amino]-ethane sulfonic acid) ......................10.0g Yeast extract......................................................10.0g α-Ketoglutarate...................................................1.0g L-Cysteine·HCl·H2O............................................0.4g Fe4(P2O7)3·9H2O...............................................0.25g pH 6.9 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 6.9. Filter sterilize. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation of Legionella pneumophila.
Caffeic Acid Ferric Citrate Test Medium (CAFC Test Medium) (Caffeic Acid Agar) Composition per liter: Agar ..................................................................20.0g (NH4)2SO4...........................................................5.0g Glucose ...............................................................5.0g Yeast extract........................................................2.0g K2HPO4 ...............................................................0.8g MgSO4·3H2O ......................................................0.7g Caffeic acid·1/2H2O ..........................................0.18g Chloramphenicol...............................................0.05g Ferric citrate solution ...................................... 4.0mL pH 6.5 ± 0.2 at 25°C
Ferric Citrate Solution: Composition per 20.0mL: Agar .............................................................100.0mg
Preparation of Ferric Citrate Solution: Add ferric citrate to 20.0mL of distilled/deionized water. Mix thoroughly.
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Preparation of Medium: Add components, except chloramphenicol, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Heat to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C. Aseptically add 0.05g of chloramphenicol. Mix thoroughly. Pour into sterile Petri dishes.
Use: For the isolation and presumptive identification of Cryptococcus neoformans. Cryptococcus neoformans appears as dark brown colonies. All other Cryptococcus species appear as light brown or nonpigmented colonies.
Caffeine Medium Composition per liter: Agar ..................................................................15.0g Solution A................................................... 400.0mL Solution B ................................................... 400.0mL Solution C ................................................... 200.0mL pH 5.0 ± 0.2 at 25°C
Solution A: Composition per 400.0mL: Na2HPO4 .............................................................7.8g KH2PO4...............................................................3.0g Caffeine...............................................................1.0g NaCl..................................................................0.58g
Preparation of Solution A: Add components to distilled/deionized water and bring volume to 400.0mL. Mix thoroughly. Adjust pH to 5.0. Solution B: Composition per 400.0mL: MgSO4·7H2O ....................................................0.12g CaCl2·2H2O ...................................................11.0mg
Preparation of Solution B: Add components to distilled/deionized water and bring volume to 400.0mL. Mix thoroughly. Solution C: Composition per 200.0mL: FeCl3 ..............................................................16.0mg
Preparation of Solution C: Add FeCl3 to dis-
tilled/deionized water and bring volume to 200.0mL. Mix thoroughly.
Preparation of Medium: To 400.0mL of solution A, add 400.0mL of solution B and 200.0mL of solution C. Adjust pH to 5.0. Add agar. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation of Pseudomonas species.
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CAL Agar
CAL Agar (Cellobiose Arginine Lysine Agar) (Yersinia Isolation Agar) Composition per liter: Agar ..................................................................20.0g L-Arginine·HCl....................................................6.5g L-Lysine·HCl .......................................................6.5g NaCl ....................................................................5.0g Cellobiose ...........................................................3.5g Yeast extract........................................................3.0g Sodium deoxycholate..........................................1.5g Neutral Red .......................................................0.03g
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Heat to boiling. Do not autoclave. Pour into sterile Petri dishes.
Use: For the isolation and characterization of Yersinia enterocolitica from fecal specimens and enumeration of Yersinia enterocolitica from water and other liquid specimens.
CAL Broth (Cellobiose Arginine Lysine Broth) Composition per liter: L-Arginine·HCl....................................................6.5g L-Lysine·HCl .......................................................6.5g
NaCl ....................................................................5.0g Cellobiose ...........................................................3.5g Yeast extract........................................................3.0g Sodium deoxycholate..........................................1.5g Neutral Red .......................................................0.03g
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Heat to boiling. Do not autoclave. Distribute into sterile tubes in 6.0–8.0mL volumes.
Use: For the isolation and characterization of Yersinia enterocolitica from fecal specimens and enumeration of Yersinia enterocolitica from water and other liquid specimens.
Calymmatobacterium granulomatis Semidefined Medium
screw-capped tubes in 20–22mL volumes. Autoclave for 15 min at 15 psi pressure–121°C. Tighten screw caps.
Use: For the cultivation of Calymmatobacterium granulomatis.
CAMG Broth Composition per liter: K2HPO4...............................................................5.0g Pancreatic digest of casein..................................5.0g Yeast extract........................................................5.0g Glucose ...............................................................2.0g Tween 80......................................................... 0.5mL pH 7.0 ± 0.1 at 25°C
Preparation of Medium: Prepare and dispense anaerobically under an atmosphere of 80% N2 + 10% CO2 + 10% H2. Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Sparge with a gas mixture of 80% N2 + 10% CO2 + 10% H2. Adjust pH to 7.5. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure– 121°C.
Use: For the cultivation of Actinomyces naeslundii.
Campy THIO Medium Composition per liter: Pancreatic digest of casein................................20.0g Agar ..................................................................15.0g NaCl....................................................................2.5g K2HPO4...............................................................1.5g Sodium thioglycolate ..........................................0.6g L-Cystine .............................................................0.4g Na2SO3 ................................................................0.2g Antibiotic supplement................................... 10.0mL
Antibiotic Supplement: Composition per 10.0mL: Cephalothin....................................................15.0mg Vancomycin ...................................................10.0mg Trimethoprim ...................................................5.0mg Amphotericin B ...............................................2.0mg Polymyxin B ................................................... 2500U
Composition per liter:
Preparation of Antibiotic Supplement: Add
Papaic digest of soybean meal ..........................20.0g NaCl ....................................................................2.5g K2HPO4 ...............................................................1.5g Sodium thioglycolate ..........................................0.6g L-Cystine .............................................................0.4g pH 7.2 ± 0.2 at 25°C
components to 10.0mL of distilled/deionized water. Filter sterilize.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.2. Distribute into
Preparation of Medium: Add components, except antibiotic solution, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 10.0mL of sterile antibiotic solution. Mix thoroughly. Aseptically distribute into sterile screw-
Campylobacter Agar, Blaser’s capped tubes in 3.0mL volumes for 1.5cm swabs or 5.0mL volumes for 3.0cm swabs.
Use: For the maintenance—as a holding or transport medium—of Campylobacter species isolated from clinical specimens on swabs.
Campylobacter Agar Composition per liter: Agar ..................................................................15.0g Polypeptone ......................................................10.0g Meat extract ........................................................5.0g NaCl ....................................................................5.0g Yeast extract........................................................5.0g Sodium L-glutamate ............................................2.0g Sodium succinate·6H2O......................................2.0g MgCl2·6H2O .......................................................1.0g Sheep blood, defibrinated ............................. 50.0mL pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Add components, except sheep blood, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Adjust pH to 7.0. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Aseptically add 50.0mL of sterile defibrinated sheep blood. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation of Moraxella lincolnii.
Campylobacter Agar with 5 Antimicrobics and 10% Sheep Blood Composition per liter: Agar ..................................................................15.0g Pancreatic digest of casein................................10.0g Peptic digest of animal tissue............................10.0g NaCl ....................................................................5.0g Yeast extract........................................................2.0g Glucose ...............................................................1.0g NaHSO3 ..............................................................0.1g Sheep blood, defibrinated ........................... 100.0mL Antibiotic supplement................................... 10.0mL pH 7.2 ± 0.2 at 25°C
Source: This medium is available as a prepared medium from BD Diagnostic Systems.
Antibiotic Supplement: Composition per 10.0mL: Cephalothin.....................................................0.015g Vancomycin ......................................................0.01g Trimethoprim ...................................................5.0mg Amphotericin B................................................2.0mg Polymyxin B ...................................................2500U
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Preparation of Antibiotic Supplement: Add components to 10.0mL of distilled/deionized water. Filter sterilize.
Preparation of Medium: Add components, except sheep blood and antibiotic solution, to distilled/ deionized water and bring volume to 890.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 100.0mL of sterile sheep blood and 10.0mL of sterile antibiotic solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the primary selective isolation and cultivation of Campylobacter jejuni from human fecal specimens.
Campylobacter Agar, Blaser’s (Blaser’s Campylobacter Agar) Composition per liter: Campylobacter agar base............................ 990.0mL Supplement B................................................ 10.0mL pH 7.4 ± 0.2 at 25°C
Campylobacter Agar Base: Composition per liter: Proteose peptone...............................................15.0g Agar ..................................................................12.0g NaCl....................................................................5.0g Yeast extract........................................................5.0g Liver digest .........................................................2.5g
Source: Campylobacter agar base and Campylobacter antimicrobic supplement B are available as a premixed powder from BD Diagnostic Systems.
Preparation of Campylobacter Agar Base: Add components to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Supplement B: Composition per 10.0mL: Cephalothin....................................................15.0mg Vancomycin ...................................................10.0mg Trimethoprim ...................................................5.0mg Amphotericin B ...............................................2.0mg Polymyxin B ................................................... 2500U
Preparation of Supplement B: Add components to 10.0mL of distilled/deionized water. Filter sterilize. Preparation of Medium: Prepare 990.0mL of Campylobacter agar base. Autoclave and cool to 45°– 50°C. Aseptically add 10.0mL of sterile supplement B. Mix thoroughly. Pour into sterile Petri dishes.
Use: For the selective isolation of Campylobacter jejuni from fecal specimens.
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Campylobacter Agar, Skirrow’s
Campylobacter Agar, Skirrow’s (Skirrow’s Campylobacter Agar) Composition per liter: Campylobacter agar base............................ 990.0mL Supplement S ................................................ 10.0mL pH 7.4 ± 0.2 at 25°C
Cefoperazone-Amphotericin B Solution: Composition per 10.0mL: Cefoperazone ..................................................0.016g Amphotericn B................................................0.005g
Preparation of Cefoperazone-Amphotericin B Solution: Add cefoperazone and amphotericin B
Campylobacter Agar Base: Composition per liter:
to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Proteose peptone ...............................................15.0g Agar ..................................................................12.0g NaCl ....................................................................5.0g Yeast extract........................................................5.0g Liver digest .........................................................2.5g
Preparation of Medium: Add components ex-
Source: Campylobacter agar base and Campylobacter antimicrobic supplement S are available as a premixed powder from BD Diagnostic Systems.
Preparation of Campylobacter Agar Base: Add components to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Supplement S: Composition per 10.0mL: Vancomycin ...................................................10.0mg Trimethoprim ...................................................5.0mg Polymyxin B ...................................................2500U
Preparation of Supplement S: Add components to 10.0mL of distilled/deionized water. Filter sterilize. Preparation of Medium: Prepare 990.0mL of Campylobacter agar base. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 10.0mL of sterile supplement S. Mix thoroughly. Pour into sterile Petri dishes.
Use: For the selective isolation of Campylobacter jejuni from fecal specimens.
Campylobacter Blood-Free Agar Base Modified (CCDA, Modified) Composition per liter: Peptone..............................................................20.0g Agar ..................................................................12.0g NaCl ....................................................................5.0g Activated charcoal ..............................................4.0g Casein hydrolysate..............................................3.0g Na-desoxycholate................................................1.0g Na-pyruvate ......................................................0.25g FeSO4 ................................................................0.25g Cefaperazone-amhotericin B solution .......... 10.0mL pH 7.4 ± 0.2 at 25°C
cept cefaperazone-amphotericin B solution to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 10.0mL of cefoperazone-amphotericin B solution. Mix thoroughly. Pour into sterile Petri dishes or aseptically distribute into tubes or flasks.
Use: For the isolation of Campylobacter spp. Amphotericin largely reduces the growth of yeasts and molds. Cefoperazone especially inhibits Enterobacteriaceae.
Campylobacter Blood-Free Selective Agar Composition per liter: Agar ..................................................................12.0g Beef extract.......................................................10.0g Peptone .............................................................10.0g Charcoal..............................................................4.0g Casein hydrolysate..............................................3.0g Sodium deoxycholate..........................................1.0g Fe2SO4·H2O ......................................................0.25g Sodium pyruvate...............................................0.25g Cefoperazone solution .................................. 10.0mL pH 7.4 ± 0.2 at 25°C
Cefoperazone Solution: Composition per 10.0mL: Sodium cefoperazone......................................0.032g
Preparation of Cefoperazone Solution: Add sodium cefoperazone to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except cefoperazone solution, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Heat with frequent agitation and boil for 1 min to completely dissolve. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Add 10.0mL of sterile cefoperazone solution. Addition of 10.0mg/L of amphotericin B improves the selectivity of the medium. Mix thoroughly. Pour into sterile Petri dishes.
Campylobacter Enrichment Broth Use: For the selective isolation of Campylobacter species, especially Campylobacter jejuni, Campylobacter coli, and Campylobacter laridis.
Campylobacter Charcoal Differential Agar (CCDA) (Preston Blood-Free Medium) Composition per liter: Agar ..................................................................12.0g Beef extract .......................................................10.0g Peptone..............................................................10.0g NaCl ....................................................................5.0g Charcoal ..............................................................4.0g Casein hydrolysate..............................................3.0g Sodium deoxycholate..........................................1.0g FeSO4 ................................................................0.25g Sodium pyruvate ...............................................0.25g Cefoperazone solution .................................. 10.0mL pH 7.5 ± 0.2 at 25°C
Cefoperazone Solution: Composition per 10.0mL: Sodium cefoperazone......................................0.032g
Preparation of Cefoperazone Solution: Add sodium cefoperazone to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. Preparation of Medium: Add components, except cefoperazone solution, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 10.0mL of sterile cefoperazone solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation of Campylobacter species.
Campylobacter Enrichment Broth (FDA Medium M29) Composition per 1024.0mL: Basal medium ............................................. 950.0mL Horse blood, lysed ........................................ 50.0mL Cefoperazone solution .................................... 8.0mL FBP solution ................................................... 4.0mL Trimethoprim lactate solution......................... 4.0mL Vancomycin solution....................................... 4.0mL Cycloheximide solution .................................. 4.0mL pH 7.5 ± 0.2 at 25°C
Basal Medium: Composition per 950.0mL: Beef extract .......................................................10.0g Peptone..............................................................10.0g
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Yeast extract........................................................6.0g NaCl....................................................................5.0g
Preparation of Basal Medium: Add components to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
FBP Solution: Composition per 100.0mL: FeSO4·7H2O......................................................6.25g Na2S2O5 ............................................................6.25g Sodium pyruvate...............................................6.25g
Preparation of FBP: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Cefoperazone Solution: Composition per 10.0mL: Cefoperazone ..................................................0.037g
Preparation of Cefoperazone Solution: Add cefoperazone to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Trimethoprim Lactate Solution: Composition per 10.0mL: Trimethoprim lactate.......................................0.031g
Preparation of Trimethoprim Lactate Solution: Add trimethoprim lactate to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Vancomycin Solution: Composition per 10.0mL: Vancomycin ....................................................0.025g
Preparation of Vancomycin Solution: Add vancomycin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. Cycloheximide Solution: Composition per 10.0mL: Cycloheximide................................................0.025g
Preparation of Cycloheximide Solution: Add cycloheximide to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. Preparation of Medium: To 950.0mL of cooled sterile basal medium, aseptically add 50.0mL of lysed (fresh, frozen, and thawed) horse blood, 4.0mL of sterile FBP solution, 8.0mL of sterile cefoperazone solution, 4.0mL of sterile trimethoprim lactate solution, 4.0mL of sterile vancomycin solution, and 4.0mL of sterile cycloheximide solution. Mix thoroughly. Aseptically distribute into sterile screwcapped tubes or bottles. Close caps tightly to reduce O2 absorbtion. Use within 2 weeks.
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Campylobacter Enrichment Broth
Use: For the selective isolation and cultivation of Campylobacter species.
Cycloheximide Solution: Composition per 10.0mL: Cycloheximide................................................0.025g
Campylobacter Enrichment Broth (FDA Medium M29) Composition per 1020.0mL: Basal medium ............................................. 950.0mL Horse blood, lysed ........................................ 50.0mL FBP solution ................................................... 4.0mL Cefoperazone solution .................................... 4.0mL Trimethoprim lactate solution......................... 4.0mL Vancomycin solution....................................... 4.0mL Cycloheximide solution .................................. 4.0mL pH 7.5 ± 0.2 at 25°C
Basal Medium: Composition per 950.0mL:
Preparation of Cycloheximide Solution: Add cycloheximide to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. Preparation of Medium: To 950.0mL of cooled, sterile basal medium, aseptically add 50.0mL of lysed (fresh, frozen, and thawed) horse blood, 4.0mL of sterile FBP solution, 4.0mL of sterile cefoperazone solution, 4.0mL of sterile trimethoprim lactate solution, 4.0mL of sterile vancomycin solution, and 4.0mL of sterile cycloheximide solution. Mix thoroughly. Aseptically distribute into sterile screwcapped tubes or bottles. Close caps tightly to reduce O2 absorption. Use within 2 weeks.
Beef extract .......................................................10.0g Peptone..............................................................10.0g Yeast extract........................................................6.0g NaCl ....................................................................5.0g
Use: For the selective isolation and cultivation of
Preparation of Basal Medium: Add compo-
Composition per 1016.0mL:
nents to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
FBP Solution: Composition per 100.0mL: FeSO4·7H2O......................................................6.25g Na2S2O5 ............................................................6.25g Sodium pyruvate ...............................................6.25g
Preparation of FBP: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Cefoperazone Solution: Composition per 10.0mL: Cefoperazone ..................................................0.037g
Preparation of Cefoperazone Solution: Add cefoperazone to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Trimethoprim Lactate Solution: Composition per 10.0mL: Trimethoprim lactate.......................................0.031g
Preparation of Trimethoprim Lactate Solution: Add trimethoprim lactate to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Vancomycin Solution: Composition per 10.0mL: Vancomycin ....................................................0.025g
Preparation of Vancomycin Solution: Add vancomycin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Campylobacter species.
Campylobacter Enrichment Broth Peptone .............................................................10.0g Yeast extract........................................................5.0g Lactalbumin hydrolysate ....................................5.0g NaCl....................................................................5.0g α-Ketoglutamic acid ...........................................1.0g Na2CO3 ...............................................................0.6g Sodium pyruvate.................................................0.5g Na2S2O5 ..............................................................0.5g Haemin..............................................................0.01g Cefoperazone solution .................................... 4.0mL Trimethoprim lactate solution......................... 4.0mL Vancomycin solution ...................................... 4.0mL Cycloheximide or amphotericin B solution.... 4.0mL pH 7.4 ± 0.2 at 25°C
Cefoperazone Solution: Composition per 10.0mL: Cefoperazone ....................................................0.05g
Preparation of Cefoperazone Solution: Add cefoperazone to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. Can be stored for 5 days at 4°C, 14 days at –20°C, and 5 months at –70°C.
Trimethoprim Solution: Composition per 10.0mL: Trimethoprim lactate.......................................0.066g
Preparation of Trimethoprim Solution: Add trimethoprim lactate to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. Alternately add 0.05g tremethoprim hydrochloride to 3.0mL 0.05N HCl. Heat to 50°C. Stir until dissolved. Add distilled/deionized water and bring
Campylobacter fetus Medium
105
volume to 10.0mL. Mix thoroughly. Filter sterilize. Can be stored for 1 year at 4°C.
Blood Agar Base: Composition per liter:
Vancomycin Solution: Composition per 10.0mL:
Beef heart, solids from infusion......................500.0g Agar ..................................................................15.0g Tryptose ............................................................10.0g NaCl....................................................................5.0g
Vancomycin ......................................................0.05g
Preparation of Vancomycin Solution: Add vancomycin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. Can be stored for 2 months at 4°C. Cycloheximide Solution: Composition per 10.0mL: Cycloheximide ................................................0.025g Ethanol ............................................................ 2.0mL
Preparation of Cycloheximide Solution: Add cycloheximide to 2.0mL ethanol to dissolve. Mix thoroughly. Add distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. Can be stored for 1 year at 4°C. Amphotericin B Solution: Composition per 10.0mL: Amphotericin B...............................................0.005g
Preparation of Amphotericin B Solution: Add amphotericin B to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. Can be stored for 1 year at –20°C.
Preparation of Blood Agar Base: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling.
Antibiotic Solution: Composition per 10.0mL: Cycloheximide..................................................0.12g Albamycin........................................................6.0mg Bacitracin........................................................ 6000U
Preparation of Antibiotic Solution: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: To 1.0L of blood agar base, add soluble starch, yeast extract, and sodium lactate. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile bovine blood and antibiotic solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes. Use: For the cultivation and isolation of Campylobacter fecalis.
Preparation of Medium: Add components, except antimicrobic solutions, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C. Aseptically add 4.0mL of sterile cefoperazone solution, 4.0mL of sterile trimethoprim lactate solution, 4.0mL of sterile vancomycin solution, and either 4.0mL of sterile cycloheximide solution of 4.0mL of sterile amphotericin B solution. Mix thoroughly. Aseptically distribute into sterile screwcapped tubes or bottles. Close caps tightly to reduce O2 absorbtion. Use within 2 weeks.
Use: For the selective isolation and cultivation of Campylobacter species.
Campylobacter fetus Medium Composition per liter: Proteose peptone...............................................10.0g NaCl....................................................................5.0g Beef extract.........................................................3.0g Bovine blood................................................. 50.0mL Antibiotic solution ........................................ 10.0mL pH 7.2–7.4 at 25°C
Antibiotic Solution: Composition per 10.0mL: Novobiocin ......................................................2.0mg Bacitracin........................................................ 2000U
Preparation of Antibiotic Solution: Add com-
Campylobacter fecalis Medium Composition per 1133.6mL: Starch, soluble.....................................................2.4g Yeast extract........................................................2.4g Blood agar base.................................................. 1.0L Bovine blood............................................... 120.0mL Antibiotic solution ........................................ 10.0mL Sodium lactate (60% syrup)............................ 3.6mL pH 6.8 ± 0.2 at 25°C
ponents to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except bovine blood and antibiotic solution, to distilled/ deionized water and bring volume to 940.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile bovine blood and antibiotic solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
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Campylobacter fetus Medium
Use: For the isolation and cultivation of Campylobacter fetus.
Campylobacter fetus Medium Composition per 1160.0mL: Fluid thioglycolate agar ..................................... 1.0L Sheep blood, defibrinated ........................... 150.0mL Antibiotic solution ........................................ 10.0mL pH 7.1 ± 0.2 at 25°C
Fluid Thioglycolate Agar: Composition per liter: Agar ..................................................................15.0g Pancreatic digest of casein................................15.0g Glucose ...............................................................5.5g Yeast extract........................................................5.0g NaCl ....................................................................2.5g Agar ..................................................................0.75g L-Cystine .............................................................0.5g Sodium thioglycolate ..........................................0.5g Resazurin .........................................................1.0mg
Preparation of Fluid Thioglycolate Agar: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C.
Antibiotic Solution: Composition per 10.0mL: Cycloheximide ..................................................0.05g Novobiocin.......................................................5.0mg Bacitracin .....................................................25,000U Polymyxin B sulfate.....................................10,000U
Preparation of Antibiotic Solution: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: To 1.0L of cooled, sterile, fluid thioglycolate agar, aseptically add 150.0mL of sterile sheep blood and 10.0mL of sterile antibiotic solution.
Use: For the isolation and cultivation of Campylobacter fetus from human specimens.
NaCl....................................................................2.5g Agar ..................................................................0.75g L-Cystine .............................................................0.5g Sodium thioglycolate ..........................................0.5g Resazurin .........................................................1.0mg
Preparation of Fluid Thioglycolate Agar: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C.
Antibiotic Solution: Composition per 10.0mL: Cycloheximide..................................................0.05g Cephalothin.......................................................0.02g Novobiocin ......................................................5.0mg Bacitracin..................................................... 25,000U Colistin.........................................................10,000U
Preparation of Antibiotic Solution: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: To 1.0L of cooled, sterile, fluid thioglycolate agar, aseptically add 150.0mL of sterile sheep blood and 10.0mL of sterile antibiotic solution.
Use: For the isolation and cultivation of Campylobacter fetus.
Campylobacter Isolation Agar A Composition per liter: Agar ..................................................................12.0g Beef extract.......................................................10.0g Peptone .............................................................10.0g NaCl....................................................................5.0g Charcoal..............................................................4.0g Casein hydrolysate..............................................3.0g Yeast extract........................................................2.0g Sodium deoxycholate..........................................1.0g FeSO4 ................................................................0.25g Sodium pyruvate...............................................0.25g Antibiotic solution ........................................ 10.0mL pH 7.4 ± 0.2 at 25°C
Composition per liter:
Antibiotic Solution: Composition per 10.0mL:
Fluid thioglycolate agar ..................................... 1.0L Sheep blood, defibrinated ........................... 150.0mL Antibiotic solution ........................................ 10.0mL
Cycloheximide....................................................0.1g Sodium cefoperazone........................................0.03g
Preparation of Antibiotic Solution: Add com-
Fluid Thioglycolate Agar: Composition per liter:
ponents to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Agar ..................................................................15.0g Pancreatic digest of casein................................15.0g Glucose ...............................................................5.5g Yeast extract........................................................5.0g
Preparation of Medium: Add components, ex-
Campylobacter fetus Selective Medium
cept antibiotic solution, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at
Campylobacter mucosalis Medium 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile antibiotic solution. Mix thoroughly. Pour into sterile Petri dishes. Swirl flask while pouring to distribute charcoal.
Use: For the isolation and cultivation of Campylobacter species.
Campylobacter Isolation Agar B (Campy Cefex Agar) Composition per liter: Agar ..................................................................15.0g Pancreatic digest of casein................................10.0g Peptic digest of animal tissue............................10.0g NaCl ....................................................................5.0g Yeast extract........................................................2.0g Glucose ...............................................................1.0g FeSO4 ..................................................................0.5g Sodium pyruvate .................................................0.5g NaHSO3 ............................................................0.35g Horse blood, laked ........................................ 50.0mL Antibiotic solution ........................................ 10.0mL pH 7.0 ± 0.2 at 25°C
Horse Blood, Laked: Composition per 50.0mL: Horse blood, fresh......................................... 50.0mL
Preparation of Horse Blood, Laked: Add blood to a sterile polypropylene bottle. Freeze overnight at −20°C. Thaw at 8°C. Refreeze at −20°C. Thaw again at 8°C. Antibiotic Solution: Composition per 10.0mL: Cycloheximide ....................................................0.1g Sodium cefoperazone......................................0.033g
Preparation of Antibiotic Solution: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except horse blood and antibiotic solution, to distilled/ deionized water and bring volume to 940.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile horse blood and antibiotic solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation and cultivation of Campylobacter species.
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Yeast extract........................................................0.2g CaCl2·2H2O ...................................................28.0mg Resazurin .........................................................1.0mg Phosphate-cysteine solution........................ 100.0mL Trace elements solution SL-10 ....................... 1.0mL pH 7.0 ± 0.2 at 25°C
Phosphate-Cysteine Solution: Composition per 100.0mL: NaH2PO4 ...........................................................0.25g L-Cysteine·HCl .................................................0.25g
Preparation of Phosphate-Cysteine Solution: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Trace Elements Solution SL-10: Composition per liter: FeCl2·4H2O .........................................................1.5g CoCl2·6H2O .................................................190.0mg MnCl2·4H2O ................................................100.0mg ZnCl2 ..............................................................70.0mg Na2MoO4·2H2O .............................................36.0mg NiCl2·6H2O ....................................................24.0mg H3BO3 ..............................................................6.0mg CuCl2·2H2O .....................................................2.0mg HCl (25% solution)....................................... 10.0mL
Preparation of Trace Elements Solution SL-10: Add FeCl2·4H2O to 10.0mL of HCl solution. Mix thoroughly. Add distilled/deionized water and bring volume to 1.0L. Add remaining components. Mix thoroughly.
Preparation of Medium: Add components, except phosphate-cysteine solution, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure– 121°C. Aseptically add 100.0mL of sterile phosphate-cysteine solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation and maintenance of Campylobacter species, Actinobacillus ureae, Erysipelothrix rhusiopathiae, Helicobacter pylori, Moraxella bovis, Moraxella nonliquefaciens, Moraxella osloensis, Pasteurella haemolytica, and Pasteurella multocida.
Campylobacter mucosalis Medium Composition per liter:
Campylobacter Medium Composition per liter: Sodium aspartate...............................................10.0g MgSO4·7H2O ..................................................... 1.0g K2HPO4 .............................................................0.75g
Agar ..................................................................15.0g Beef extract.......................................................10.0g Special peptone.................................................10.0g NaCl....................................................................5.0g Sodium fumarate.................................................3.0g
108
Campylobacter rectus Medium
Sodium formate...................................................2.0g Horse blood, defibrinated ............................. 50.0mL pH 7.2 ± 0.2 at 25°C
sterile hemin solution under 100% N2. Mix thoroughly. Aseptically and anaerobically distribute into sterile anaerobic tubes.
Source: Special peptone (L72) is available from
Use: For the cultivation and maintenance of Campy-
Oxoid Unipath.
lobacter curvus and Campylobacter rectus.
Preparation of Medium: Add components, except horse blood, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Heat with frequent agitation and boil for 1 min to completely dissolve. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C. Aseptically add 50.0mL of sterile, defibrinated horse blood. Mix thoroughly and pour into sterile Petri dishes.
Use: For the cultivation and maintenance of Campylobacter mucosalis.
Campylobacter rectus Medium Composition per liter: Yeast extract......................................................11.0g Pancreatic digest of casein..................................9.0g Beef extract .........................................................3.0g NaCl ....................................................................2.0g Na2HPO4 .............................................................0.4g Na2CO3 .............................................................0.25g Resazurin .........................................................1.0mg Formate-fumarate solution.......................... 100.0mL Hemin solution.............................................. 10.0mL pH 7.5 ± 0.2 at 25°C
Formate-Fumarate Solution: Composition per 100.0mL: Sodium fumarate.................................................3.0g Sodium formate...................................................2.0g
Preparation of Formate-Fumarate Solution: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize. Sparge with 100% N2 for 3–4 min. Hemin Solution: Composition per 10.0mL: Hemin...............................................................5.0mg NaOH (1N solution)........................................ 0.1mL
Preparation of Hemin Solution: Add hemin to NaOH solution to dissolve. Add distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Sparge with 100% N2 for 3–4 min. Autoclave under 100% N2 for 15 min at 15 psi pressure–121°C.
Preparation of Medium: Add components, except formate-fumarate solution and hemin solution, to distilled/deionized water and bring volume to 890.0mL. Sparge with 100% N2 for 10 min. Autoclave under 100% N2 for 15 min at 15 psi pressure– 121°C. Aseptically and anaerobically add 100.0mL of sterile formate-fumarate solution and 10.0mL of
Campylobacter Selective Medium, Blaser-Wang (Blaser-Wang Campylobacter Medium) (Blaser’s Agar) (Campy BAP Medium) Composition per liter: Brucella agar base....................................... 890.0mL Sheep blood ................................................ 100.0mL Antibiotic supplement................................... 10.0mL
Brucella Agar Base: Composition per 890.0mL: Agar ..................................................................15.0g Glucose .............................................................10.0g Pancreatic digest of casein................................10.0g NaCl....................................................................5.0g Peptic digest of animal tissue .............................5.0g pH 7.5 ± 0.2 at 25°C
Preparation of Brucella Agar Base: Add components to distilled/deionized water and bring volume to 890.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Antibiotic Supplement: Composition per 10.0mL: Cephalothin....................................................15.0mg Vancomycin ...................................................10.0mg Trimethoprim ...................................................5.0mg Amphotericin B ...............................................2.0mg Polymyxin B ................................................... 2500U
Preparation of Antibiotic Supplement: Add components to 10.0mL of distilled/deionized water. Filter sterilize.
Preparation of Medium: Prepare 890.0mL of Brucella agar base. Sterilize as directed. Cool to 50°– 55°C and add 100.0mL of sheep blood or 50.0– 70.0mL of laked horse blood. Laked blood is prepared by freezing whole blood overnight and thawing to room temperature. Aseptically add 10.0mL of sterile antibiotic supplement. Mix thoroughly. Pour into sterile Petri dishes.
Use: For the selective isolation of Campylobacter species.
Campylobacter Selective Medium, Butzler’s
Campylobacter Selective Medium, Blaser-Wang (Blaser-Wang Campylobacter Medium) Composition per liter:
109
Pancreatic digest of casein................................10.0g NaCl....................................................................5.0g Peptic digest of animal tissue .............................5.0g
Preparation of Brucella Agar Base: Add com-
Columbia agar base..................................... 890.0mL Sheep blood................................................. 100.0mL Antibiotic supplement................................... 10.0mL pH 7.3 ± 0.2 at 25°C
ponents to distilled/deionized water and bring volume to 940.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Columbia Agar Base: Composition per liter:
Antibiotic Supplement: Composition per 10.0mL:
Special peptone .................................................25.0g Agar ..................................................................10.0g NaCl ....................................................................5.0g Starch ..................................................................1.0g
Preparation of Columbia Agar Base: Add
Cycloheximide...............................................50.0mg Cephazolin .....................................................15.0mg Novobiocin ......................................................5.0mg Bacitracin..................................................... 25,000U Colistin sulfate ............................................. 10,000U
components to distilled/deionized water and bring volume to 890.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Preparation of Antibiotic Supplement: Add
Antibiotic Supplement: Composition per 10.0mL:
sterile Brucella agar base, aseptically add 50.0mL of defibrinated sheep or horse blood and 10.0mL of sterile antibiotic supplement. Mix thoroughly. For enhanced growth, medium may also be supplemented with 0.25g of Fe2SO4·H2O, 0.25g of sodium metabisulfite, and 0.25g of sodium pyruvate. Pour into sterile Petri dishes.
Cephalothin....................................................15.0mg Vancomycin ...................................................10.0mg Trimethoprim ...................................................5.0mg Amphotericin B................................................2.0mg Polymyxin B ..................................................2,500U
Preparation of Antibiotic Supplement: Add components to 10.0mL of distilled/deionized water. Filter sterilize.
Preparation of Medium: To 890.0mL of cooled, sterile Columbia agar base, aseptically add 100.0mL of sheep blood or 50.0–70.0mL of laked horse blood. Laked blood is prepared by freezing whole blood overnight and thawing to room temperature. Aseptically add 10.0mL of sterile antibiotic supplement. Mix thoroughly. Pour into sterile Petri dishes.
Use: For the selective isolation of Campylobacter species.
Campylobacter Selective Medium, Butzler’s (Butzler’s Campylobacter Medium) Composition per liter: Brucella agar base....................................... 940.0mL Sheep or horse blood, defibrinated ............... 50.0mL Antibiotic supplement................................... 10.0mL pH 7.5 ± 0.2 at 25°C
Brucella Agar Base: Composition per liter: Agar ..................................................................15.0g Glucose .............................................................10.0g
components to 10.0mL of distilled/deionized water. Filter sterilize.
Preparation of Medium: To 940.0mL of cooled,
Use: For the selective isolation of Campylobacter species.
Campylobacter Selective Medium, Butzler’s (Butzler’s Campylobacter Medium) Composition per liter: Columbia agar base..................................... 940.0mL Blood, horse or sheep ................................... 50.0mL Antibiotic supplement................................... 10.0mL pH 7.3 ± 0.2 at 25°C
Columbia Agar Base: Composition per liter: Peptone .............................................................25.0g Agar ..................................................................10.0g NaCl....................................................................5.0g Starch ..................................................................1.0g
Preparation of Columbia Agar Base: Add components to distilled/deionized water and bring volume to 940.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Antibiotic Supplement: Composition per 10.0mL: Cycloheximide...............................................50.0mg
110
Campylobacter Selective Medium, Karmali’s
Cephazolin .....................................................15.0mg Novobiocin.......................................................5.0mg Bacitracin .....................................................25,000U Colistin sulfate .............................................10,000U
Preparation of Antibiotic Supplement: Add components to 10.0mL of distilled/deionized water. Filter sterilize.
Preparation of Medium: To 940.0mL of cooled, sterile Columbia agar base, aseptically add 50.0mL of defibrinated sheep or horse blood and 10.0mL of sterile antibiotic supplement. Mix thoroughly. The medium may also be supplemented with 0.25g of Fe2SO4·H2O, 0.25g of sodium metabisulfite, and 0.25g of sodium pyruvate. Pour into sterile Petri dishes.
Use: For the selective isolation of Campylobacter species.
Campylobacter Selective Medium, Karmali’s (Karmali’s Campylobacter Medium) Composition per liter: Activated charcoal ..............................................4.0g Columbia agar base..................................... 990.0mL Antibiotic supplement................................... 10.0mL pH 7.4 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath.
Columbia Agar Base: Composition per 990.0mL: Peptone..............................................................25.0g Agar ..................................................................10.0g NaCl ....................................................................5.0g Starch ..................................................................1.0g
Preparation of Columbia Agar Base: Add
concentration of 5–7%. Add 10.0mL of sterile antibiotic supplement. Mix thoroughly. For enhanced growth, medium may also be supplemented with 0.25g of Fe2SO4·H2O, 0.25g of sodium metabisulfite, and 0.25g of sodium pyruvate. Pour into sterile Petri dishes. Swirl while pouring to keep charcoal in suspension.
Use: For the selective isolation of Campylobacter species.
Campylobacter Selective Medium, Preston’s (Preston’s Campylobacter Medium) Composition per liter: Campylobacter agar base............................ 940.0mL Horse blood, lysed ........................................ 50.0mL Antibiotic supplement................................... 10.0mL pH 7.5 ± 0.2 at 25°C
Campylobacter Agar Base: Composition per liter: Agar ..................................................................12.0g Beef extract.......................................................10.0g Peptone .............................................................10.0g NaCl....................................................................5.0g
Preparation of Campylobacter Agar Base: Add components to distilled/deionized water and bring volume to 940.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Antibiotic Supplement: Composition per 10.0mL: Cycloheximide....................................................0.1g Rifampicin ........................................................0.01g Trimethoprim lactate.........................................0.01g Polmyxin B ..................................................... 5000U
components to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Preparation of Antibiotic Supplement: Add
Antibiotic Supplement: Composition per 10.0mL:
sterile Campylobacter agar base, aseptically add 50.0mL of lysed horse blood and 10.0mL of sterile antibiotic supplement. Mix thoroughly. Pour into sterile Petri dishes.
Sodium pyruvate ...............................................0.05g Cycloheximide ..................................................0.05g Cefoperazone ..................................................0.016g Hemin..............................................................0.016g Vancomycin ......................................................0.01g
Preparation of Antibiotic Supplement: Add components to 10.0mL of distilled/deionized water. Filter sterilize.
Preparation of Medium: Prepare 990.0mL of Columbia agar base. Sterilize as directed. Cool to 50°– 55°C. Add defibrinated sheep or horse blood to a final
components to 10.0mL of 50:50 acetone:distilled/ deionized water. Filter sterilize.
Preparation of Medium: To 940.0mL of cooled,
Use: For the selective isolation of Campylobacter species.
Campylobacter sputorum Subspecies bubulus Medium Composition per liter: Agar ....................................................................1.5g Brilliant Green ..................................................0.01g Ethyl Violet....................................................1.25mg
Candida BCG Agar Base
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Brucella broth base ............................................ 1.0L Antibiotic solution ........................................ 10.0mL pH 7.0 ± 0.2 at 25°C
Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C. Aseptically distribute into sterile tubes or flasks.
Brucella Broth Base: Composition per liter:
Use: For the cultivation and isolation of Campylo-
Pancreatic digest of casein................................10.0g Peptic digest of animal tissue............................10.0g NaCl ....................................................................5.0g Yeast extract........................................................2.0g Glucose ...............................................................1.0g NaHSO3 ..............................................................0.1g
Preparation of Brucella Broth Base: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly.
Antibiotic Solution: Composition per 10.0mL: Cycloheximide ....................................................0.1g Bacitracin .....................................................20,000U
Preparation of Antibiotic Solution: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: To 1.0L of Brucella broth base, add agar, Brilliant Green, and Ethyl Violet. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile antibiotic solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks. Use: For the cultivation and isolation of Campylobacter sputorum subspecies bubulus.
Campylobacter sputorum Subspecies mucosalis Medium Composition per liter: Yeast extract........................................................2.8g KNO3 ..................................................................1.0g Fluid thioglycolate broth without glucose ......... 1.0L
Fluid Thioglycolate Broth without Glucose: Composition per liter: Pancreatic digest of casein................................15.0g Yeast extract........................................................5.0g NaCl ....................................................................2.5g Agar ..................................................................0.75g L-Cystine .............................................................0.5g Sodium thioglycolate ..........................................0.5g Resazurin .........................................................1.0mg
Preparation of Fluid Thioglycolate Broth without Glucose: Add components to distilled/ deionized water and bring volume to 1.0L. Mix thoroughly.
Preparation of Medium: Combine components. Mix thoroughly. Gently heat and bring to boiling.
bacter sputorum subspecies mucosalis.
Campylobacter Thioglycolate Medium with 5 Antimicrobics Composition per liter: Pancreatic digest of casein................................17.0g Glucose ...............................................................6.0g Papaic digest of soybean meal............................3.0g NaCl....................................................................2.5g Agar ....................................................................1.6g Sodium thioglycolate ..........................................0.5g Na2SO3 ................................................................0.1g Antibiotic supplement solution..................... 10.0mL pH 7.0 ± 0.2 at 25°C
Antibiotic Supplement Solution: Composition per 10.0mL: Cephalothin.....................................................0.015g Vancomycin ......................................................0.01g Trimethoprim ...................................................5.0mg Amphotericin B ...............................................2.0mg Polymyxin B ................................................... 2500U
Preparation of Antibiotic Supplement Solution: Add components to 10.0mL of distilled/deionized water. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except cephalothin, vancomycin, trimethoprim, amphotericin, and polymyxin B, to distilled deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Add 10.0mL of sterile antibiotic supplement. Mix thoroughly. Pour into sterile Petri dishes.
Use: For the maintenence—as a holding medium or transport medium— of fecal specimens or swabs suspected of containing Campylobacter jejuni or other Campylobacter species when immediate inoculation of Campylobacter growth medium is unavailable.
Candida BCG Agar Base (Candida Bromcresol Green Agar Base) Composition per liter: Glucose .............................................................40.0g Agar ..................................................................15.0g Peptone .............................................................10.0g Yeast extract........................................................1.0g Bromcresol Green.............................................0.02g Neomycin solution........................................ 10.0mL pH 6.1 ± 0.1 at 25°C
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Candida Isolation Agar
Source: This medium is available as a premixed
Capnocytophaga Medium
powder from BD Diagnostic Systems.
Composition per liter:
Neomycin Solution: Composition per 10.0mL:
Pancreatic digest of casein................................17.0g KNO3 ..................................................................3.0g NaCl....................................................................3.0g Yeast extract........................................................3.0g Hemin ..............................................................3.0mg Glucose solution ........................................... 20.0mL pH 7.0 ± 0.2 at 25°C
Neomycin............................................................0.5g
Preparation of Neomycin Solution: Add neomycin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except neomycin solution, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly and heat gently until boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Aseptically add 10.0mL of sterile neomycin solution. Mix thoroughly. Pour into sterile Petri dishes or leave in tubes.
Use: For the selective isolation and identification of Candida species. It is a highly differential medium that is used for demonstrating morphological and biochemical reactions characterizing different Candida species. Candida albicans appears as blunt conical colonies with smooth edges and yellow to bluegreen color. Candida stellatoidea appears as convex colonies with smooth edges and yellow to green color. Candida tropicalis appears as convex colonies with wavy edges and yellow-green to green color with a dark blue-green base. Candida pseudotropicalis appears as convex, shiny colonies with smooth edges and green color with a light green edge. Candida krusei appears as low conical colonies with spreading edges and blue-green color. Candida stellatoidea appears as convex colonies with smooth edges and yellow to green color.
Candida Isolation Agar Composition per liter: Agar ..................................................................20.0g Glucose .............................................................10.0g Peptone................................................................5.0g Yeast extract........................................................3.0g Malt extract .........................................................3.0g Aniline Blue........................................................0.1g pH 5.9 ± 0.5 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Glucose Solution: Composition per 20.0mL: D-Glucose ............................................................3.0g
Preparation of Glucose Solution: Add glucose to distilled/deionized water and bring volume to 20.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Preparation of Medium: Add components, except glucose solution, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Aseptically add 10.0mL of sterile glucose solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation and maintenance of Capnocytophaga species.
Capnocytophaga II Medium (DSMZ Medium 779) Composition per liter: Proteose peptone no. 3......................................10.0g Yeast extract........................................................5.0g Na2HPO4 .............................................................4.0g Lab-Lemco meat extract .....................................2.4g Glucose ...............................................................1.5g Starch, soluble.....................................................0.5g Cysteine-HCl·H2O ..............................................0.5g Horse blood................................................... 50.0mL pH 6.8 ± 0.2 at 25°C
Preparation of Medium: Add components, except horse blood, to distilled/deionized water and bring volume to 950.0L. Mix thoroughly. Adjust pH to 7.6-7.8. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to room temperature. Aseptically add 50.0mL horse blood. Mix thoroughly. Aseptically distribute into tubes or flasks. Incubate under 95% air + 5% CO2 or anaerobically under 95% N2 + 5% CO2.
Use: For the cultivation of Capnocytophaga haemolytica and Capnocytophaga granulosa.
Carbohydrate Fermentation Broth
Use: For the isolation and differentiation of Candida
Composition per liter:
albicans. Candida albicans turns the medium blue.
Peptone .............................................................10.0g
Carbon Assimilation Medium, Auxanographic Method for Yeast Identification NaCl ....................................................................5.0g Meat extract ........................................................3.0g Carbohydrate solution................................... 50.0mL Andrade’s indicator....................................... 10.0mL pH 7.1 ± 0.2 at 25°C
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clave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Mineral Base Medium: Composition per 500.0mL:
Acid Fuchsin ......................................................0.1 g NaOH (1N solution)...................................... 16.0mL
Carbohydrate.....................................................10.0g NaCl....................................................................5.0g NH4HPO4 ............................................................1.0g K2HPO4...............................................................1.0g MgSO4·7H2O, anhydrous ...................................0.1g
Preparation of Andrade’s Indicator: Add
Preparation of Mineral Base Medium: Add
components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly.
components to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Gently heat until dissolved. Filter sterilize. Warm to 45°–50°C.
Andrade’s Indicator: Composition per 100.0mL:
Carbohydrate Solution: Composition per 100.0mL: Carbohydrate.....................................................10.0g
Preparation of Carbohydrate Solution: Add carbohydrate to distilled/deionized water and bring volume to 100.0mL. Adonitol, arabinose, cellobiose, glucose, dulcitol, fructose, galactose, inositol, lactose, maltose, mannitol, raffinose, rhamnose, salicin, sorbitol, sucrose, trehalose, xylose, or other carbohydrates may be used. Mix thoroughly. Filter sterilize.
Caution: Acid Fuchsin is a potential carcinogen and care must be taken to avoid inhalation of the powdered dye and contact with the skin.
Preparation of Medium: Combine 500.0mL of cooled, sterile agar solution and 500.0mL of sterile mineral base medium. Mix thoroughly. Aseptically distribute into sterile tubes. Allow tubes to cool in a slanted position.
Use: For the cultivation and differentiation of microorganisms based on their ability to utilize a particular carbon source.
Carbon Assimilation Medium, Auxanographic Method for Yeast Identification
Preparation of Medium: Add components, ex-
Composition per liter:
cept carbohydrate solution, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute in 10.0mL volumes into test tubes containing inverted Durham tubes. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 25°C. Add 0.5mL of sterile carbohydrate solution to each tube.
Noble agar.........................................................20.0g (NH4)2SO4 ..........................................................0.5g KH2PO4...............................................................0.1g MgSO4·7H2O ....................................................0.05g NaCl..................................................................0.01g CaCl2·2H2O ......................................................0.01g DL-Methionine..................................................2.0mg DL-Tryptophan..................................................2.0mg L-Histidine·HCl ................................................1.0mg Inositol .............................................................0.2mg H3BO3 ............................................................0.05mg ZnSO4·7H2O ..................................................0.04mg MnSO4·4H2O .................................................0.04mg Thiamine·HCl ................................................0.04mg Pyroxidine·HCl ..............................................0.04mg Niacin.............................................................0.04mg Calcium pantothenate ....................................0.04mg p-Aminobenzoic acid.....................................0.02mg Riboflavin ......................................................0.02mg FeCl3 ..............................................................0.02mg Na2MoO4·4H2O .............................................0.02mg KI ...................................................................0.01mg CuSO4·5H2O .....................................................4.0µg Folic acid ..........................................................0.2µg Biotin ................................................................0.2µg pH 4.5 ± 0.2 at 25°C
Use: For the determination of carbohydrate fermentation reactions of microorganisms, particularly members of the Enterobacteriaceae. A Durham tube is used to collect gas produced during the fermentation reaction. Acid production is indicated by a pink reaction.
Carbon Assimilation Medium Composition per liter: Agar solution............................................... 500.0mL Mineral base medium.................................. 500.0mL pH 6.5 ± 0.1 at 25°C
Agar Solution: Composition per liter: Agar ..................................................................32.0g
Preparation of Agar Solution: Add agar to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Auto-
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Carbon Utilization Test
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into screw-capped tubes in 20.0mL volumes. Autoclave for 15 min at 15 psi pressure– 121°C.
Use: For carbohydrate assimilation tests by the auxanographic method for the identification of yeasts.
Carbon Utilization Test Composition per liter: Ionagar ..............................................................10.0g NH4Cl .................................................................1.0g MgSO4·7H2O ......................................................0.5g Ferric ammonium citrate...................................0.05g CaCl2 ................................................................0.5mg Sodium potassium phosphate buffer (0.33M solution, pH 6.8)................... 1.0L Carbon source ............................................... 10.0mL pH 6.8 ± 0.2 at 25°C
Carbon Source: Composition per 10.0mL:
Buffered Salts Solution: Composition per liter: Na2PHO4 ........................................................284.0.g KH2PO4..........................................................272.0.g NaCl....................................................................5.0g FeSO4·7H2O........................................................4.0g MgSO4·7H2O ......................................................4.0g ZnSO4·7H2O .......................................................0.4g MnSO4·H2O ........................................................0.3g CuSO4·5H2O .....................................................0.05g
Preparation of Buffered Salts Solution: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly.
Vitamin Solution: Composition per liter: Pyridoxine·HCl ................................................2.0mg Calcium pantothenate ......................................1.0mg Nicotinamide....................................................1.0mg Thiamine·HCl ..................................................1.0mg Biotin ...............................................................0.1mg
Preparation of Vitamin Solution: Add compo-
Carbon source .....................................................1.0g
nents to distilled/deionized water and bring volume to 1.0L. Mix thoroughly.
Preparation of Carbon Source: Add carbon
Preparation of Medium: Add components to
source to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.0. Filter sterilize.
Preparation of Medium: Add components, ex-
Use: For the isolation and cultivation of Cardiobac-
cept carbon source, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile carbon source. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation and differentiation of Pseudomonas species based on their ability to utilize a specific carbon source.
Cardiobacterium hominis Medium Composition per liter: Glucose ...............................................................5.0g Leucine..............................................................0.43g Threonine ..........................................................0.28g Glutamic acid ......................................................0.2g Valine ................................................................0.19g Glycine..............................................................0.18g Arginine ............................................................0.16g Histidine............................................................0.13g Proline.................................................................0.1g Tyrosine ............................................................0.04g Buffered salts solution ................................ 100.0mL Vitamin solution............................................ 10.0mL pH 7.0 ± 0.2 at 25°C
terium hominis.
Cardiobacterium hominis Medium Composition per liter: K2HPO4...............................................................7.0g Yeast extract........................................................5.0g KH2PO4...............................................................3.0g (NH4)2SO4 ..........................................................0.1g MgSO4·7H2O ....................................................0.01g pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of Cardiobacterium hominis.
Carnitine Chloride Medium Composition per liter: Noble agar.........................................................15.0g DL-Carnitine chloride ........................................10.0g Na2HPO4 ...........................................................10.0g KH2PO4...............................................................5.5g (NH4)2HPO4........................................................2.0g NH4H2PO4 ..........................................................1.5g MgSO4·7H2O ......................................................0.2g
Cary and Blair Transport Medium, Modified Yeast extract......................................................0.05g CaCl2 ...............................................................0.015g Fe2(SO4)3 .........................................................0.6mg CuSO4·5H2O ....................................................0.2mg MnSO4·H2O .....................................................0.2mg ZnSO4·7H2O ....................................................0.2mg pH 7.0 ± 0.1 at 25°C
Preparation of Medium: Add components to
115
Na2HPO4 .............................................................1.1g CaCl2 solution................................................. 9.0mL pH 8.0 ± 0.5 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems and Oxoid Unipath.
CaCl2 Solution: Composition per 10.0mL:
distilled/deionized water and bring volume to 1.0L. Adjust pH to 7.0 with NaOH. Mix thoroughly. Heat gently until boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Preparation of CaCl2 Solution: Add CaCl2 to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Use: For the cultivation and maintenance of bacteria
Preparation of Medium: Add components to
that can use carnitine as a carbon source.
Carrot Potato Dextrose Agar (ATCC Medium 1829) Composition per liter: Agar ..................................................................25.0g Glucose .............................................................20.0g Pancreatic digest of casein..................................2.5g Yeast extract........................................................0.5g MgSO4·7H2O ......................................................0.3g CaCO3 .................................................................0.2g Potatoes, infusion from ............................... 500.0mL Carrot juice (any commercial brand) ............ 15.0 ml pH 5.6 ± 0.2 at 25°C
Source: Potato dextrose agar, without carrot juice is available as a premixed powder from BD Diagnostic Systems.
Potato Infusion: Composition per 500.0mL: Potatoes...........................................................300.0g
Preparation of Potato Infusion: Peel and dice potatoes. Add 500.0mL of distilled/deionized water. Gently heat and bring to boiling. Continue boiling for 30 min. Filter through cheesecloth. Reserve filtrate.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation of yeasts and molds. Also used to induce sporulation in many fungi.
Cary and Blair Transport Medium Composition per liter: Agar ....................................................................5.0g NaCl ....................................................................5.0g Sodium thioglycolate ..........................................1.5g
CaCl2 ...................................................................0.1g
distilled/deionized water and bring volume to 1.0L. Mix thoroughly and heat gently until boiling. Cool to 50°C. Add 9.0mL of a 1% CaCl2 solution. Adjust the pH to 8.4. Distribute into screw-capped tubes in 7.0mL volumes. Sterilize under flowing steam for 15 min. After sterilization, tighten the screwcaps.
Use: For the maintenance—as a holding medium or transport medium—of clinical specimens during collection or shipment.
Cary and Blair Transport Medium, Modified Composition per liter: Agar ....................................................................5.0g NaCl....................................................................5.0g Sodium thioglycolate ..........................................1.5g L-Cysteine·HCl·H2O............................................0.5g CaCl2·2H2O ........................................................0.1g Na2HPO4 .............................................................0.1g NaHSO3 ..............................................................0.1g Resazurin solution .......................................... 4.0mL pH 8.4 ± 0.2 at 25°C
Resazurin Solution: Composition per 380.0mL: Resazurin ..........................................................0.05g Ethanol (95% solution) ............................... 200.0mL
Preparation of Resazurin Solution: Add resazurin to 200.0mL of ethanol. Mix thoroughly. Bring volume to 380.0mL with distilled/deionized water.
Preparation of Medium: Add components, except L-cysteine·HCl·H2O, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gas the solution with 100% CO2 for 10–15 min. Add the L-cysteine·HCl·H2O. Mix thoroughly. Adjust pH to 8.4. Anaerobically distribute into tubes under 100% N2. Cap tubes with butyl rubber stoppers. Autoclave for 15 min at 0 psi pressure–100°C on three consecutive days.
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Casamino Acids Yeast Extract Lincomycin Medium
Use: For the maintenance—as a holding medium— of clinical specimens during collection or shipment.
Casamino Acids Yeast Extract Lincomycin Medium Composition per liter: Casamino acids .................................................20.0g K2HPO4 ............................................................8.71g Yeast extract........................................................6.0g NaCl ....................................................................2.5g Lincomycin solution ....................................... 5.0mL Trace salts solution ......................................... 1.0mL pH 8.5 ± 0.2 at 25°C
Lincomycin Solution: Composition per 5.0mL: Lincomycin ....................................................45.0mg
Preparation of Lincomycin Solution: Add lincomycin to distilled/deionized water and bring volume to 5.0mL. Mix thoroughly. Filter sterilize.
Trace Salts Solution: Composition per liter: MgSO4·7H2O ....................................................50.0g MnCl2· 4H2O ......................................................5.0g FeCl2 ...................................................................5.0g
Trace Salts Solution: Composition per liter: MgSO4·7H2O ....................................................50.0g MnCl2· 4H2O ......................................................5.0g FeCl2 ...................................................................5.0g
Preparation of Trace Salts Solution: Add components to distilled/deionized water and bring volume to 1.0L. Add sufficient 0.1N H2SO4 to dissolve components. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except trace salts solution, to distilled/deionized water and bring volume to 999.0mL. Mix thoroughly. Adjust pH to 8.5. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C. Aseptically add 1.0mL of sterile trace salts solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation of enterotoxigenic Escherichia coli.
Casein Agar Composition per liter: Agar ..................................................................10.0g Skim milk...................................................... 50.0mL
Preparation of Medium: Add components to
ponents to distilled/deionized water and bring volume to 1.0L. Add sufficient 0.1N H2SO4 to dissolve components. Mix thoroughly. Filter sterilize.
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Preparation of Medium: Add components, ex-
Use: For the cultivation and differentiation of aerobic
cept trace salts solution and lincomycin solution, to distilled/deionized water and bring volume to 994.0mL. Mix thoroughly. Adjust pH to 8.5. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C. Aseptically add 1.0mL of sterile trace salts solution and 5.0mL of sterile lincomycin solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
actinomycetes based on casein utilization. Bacteria that utilize casein, such as Streptomyces and Actinomadura species, appear as colonies surrounded by a clear zone. Nocardia asteroides, Nocardia caviae, and Mycobacterium fortuitum do not utilize casein.
Use: For the cultivation of heat-labile, toxin-produc-
Composition per liter:
Preparation of Trace Salts Solution: Add com-
ing enterotoxigenic Escherichia coli.
Casamino Acids Yeast Extract Salts Broth, Gorbach (CA YE Broth)
Casein Yeast Extract Glucose Agar (CYG Agar) Agar ..................................................................20.0g Glucose ...............................................................5.0g Casein hydrolysate..............................................5.0g Yeast extract........................................................5.0g pH 7.0 ± 0.2 at 25°C
Composition per liter:
Preparation of Medium: Add components to
Casamino acids .................................................20.0g K2HPO4 ............................................................8.71g Yeast extract........................................................6.0g NaCl ....................................................................2.5g Trace salts solution ......................................... 1.0mL pH 8.5 ± 0.2 at 25°C
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For agar dilution susceptibility tests with imidazole antifungal agents.
CASO MUG Agar
Casein Yeast Extract Glucose Broth (CYG Broth) Composition per liter: Casein hydrolysate..............................................5.0g Glucose ...............................................................5.0g Yeast extract........................................................5.0g pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For agar dilution susceptibility tests with imidazole antifungal agents.
Casman Agar Base Composition per liter: Noble agar.........................................................14.0g Proteose peptone no. 3 ......................................10.0g Tryptose ............................................................10.0g NaCl ....................................................................5.0g Beef extract .........................................................3.0g Cornstarch...........................................................1.0g Glucose ...............................................................0.5g p-Aminobenzoic acid........................................0.05g Nicotinamide.....................................................0.05g Blood............................................................. 50.0mL Water-lysed blood solution ............................. 1.5mL pH 7.3 ± 0.2 at 25°C
Water-Lysed Blood Solution: Composition per 8.0mL: Blood............................................................... 2.0mL
Preparation of Water-Lysed Blood Solution: Add blood to distilled/deionized water and bring volume to 8.0mL. Mix thoroughly. Filter sterilize.
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Casman Agar Base with Rabbit Blood (Casman-Medium) (DSMZ Medium 439) Composition per liter: Noble agar.........................................................14.0g Proteose peptone no. 3......................................10.0g Tryptose ............................................................10.0g NaCl....................................................................5.0g Beef extract.........................................................3.0g Cornstarch...........................................................1.0g Glucose ...............................................................0.5g p-Aminobenzoic acid........................................0.05g Nicotinamide.....................................................0.05g Rabbit blood.................................................. 50.0mL Water-lysed blood solution ............................. 1.5mL pH 7.3 ± 0.2 at 25°C
Source: Casman agar base is available as a premixed powder from BD Diagnostic Systems.
Water-Lysed Blood Solution: Composition per 8.0mL: Rabbit blood.................................................... 2.0mL
Preparation of Water-Lysed Blood Solution: Add blood to distilled/deionized water and bring volume to 8.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except rabbit blood and water-lysed blood solution, to distilled/deionized water and bring volume to 950.0L. Mix thoroughly. Gently heat to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C. Aseptically add 50.0mL of sterile rabbit blood and 1.5mL of sterile water-lysed blood solution. Water-lysed blood may be omitted if sterile blood is partially lysed due to storage. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation and maintenance of Gardnerella vaginalis.
Preparation of Medium: Add components, except blood and water-lysed blood solution, to distilled/deionized water and bring volume to 948.5mL. Mix thoroughly. Gently heat to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C. Aseptically add 50.0mL of sterile blood and 1.5mL of sterile water-lysed blood solution (one part blood to three parts water). Water-lysed blood may be omitted if sterile blood is partially lysed due to storage. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation of fastidious bacteria from clinical specimens. For the cultivation under reduced oxygen tension of fastidious microorganisms such as Haemophilus influenzae, Neisseria meningitidis, and Neisseria gonorrhoeae.
CASO MUG Agar Composition per liter: Casein peptone..................................................16.0g Agar ..................................................................13.0g NaCl....................................................................6.0g Soy peptone ........................................................5.0g Tryptophan..........................................................1.0g 4-Methylumbelliferyl-β-D-glucuronide ............0.07g pH 7.3 ± 0.2 at 25°C
Source: This medium is available from Fluka, Sigma-Aldrich.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring
118
CCY Modified Medium
to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 50°C. Pour into sterile Petri dishes.
Use: This universal medium without indicator or inhibitor is intended for a broad range of application including enumeration and cultivation of a wide variety of microorganisms. It is also suitable for the cultivation of more fastidious microorganisms. β-D-glucoronidase, which is produced by E. coli, cleaves 4methylumbelliferyl-β-D-glucuronide to 4-methylumbelliferone and glucuronide. The fluorogen 4-methylumbelliferone can be detected under a long wavelength UV lamp. A positive indole reaction provides confirmation.
CCY Modified Medium Composition per liter: Yeast extract..................................................... 30.0g Casamino acids .................................................20.0g Na2HPO4 ..........................................................2.48g KH2PO4 .............................................................0.41g MgSO4·7H2O .................................................20.0mg MnSO4·H2O .....................................................7.5mg Citric acid.........................................................6.4mg FeSO4·7H2O.....................................................6.4mg Sodium pyruvate solution ......................... 100.00mL pH 7.3 ± 0.2 at 25°C
Vitamin K1 solution ........................................ 1.0mL Hemin solution................................................ 0.5mL pH 7.5 ± 0.2 at 25°C
Source: This medium is available as a prepared medium from BD Diagnostic Systems.
Vitamin K1 Solution: Composition per 100.0mL: Vitamin K1 ..........................................................1.0g Ethanol.......................................................... 99.0mL
Preparation of Vitamin K1 Solution: Add vitamin K1 to 99.0mL of absolute ethanol. Mix thoroughly. Filter sterilize.
Hemin Solution: Composition per 100.0mL: Hemin .................................................................1.0g NaOH (1N solution)...................................... 20.0mL
Preparation of Hemin Solution: Add hemin to 20.0mL of 1N NaOH solution. Mix thoroughly. Bring volume to 100.0mL with distilled/deionized water.
Preparation of Medium: Add components, ex-
Sodium Pyruvate Solution: Composition per 100.0mL:
cept vitamin K1 and sheep blood, to distilled/deionized water and bring volume to 949.0mL. Mix thoroughly. Heat gently and bring to boiling for 1 min. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Aseptically add 1.0mL of vitamin K1 solution and 50.0mL of sterile, defibrinated sheep blood. Mix thoroughly. Pour into sterile Petri dishes.
Sodium pyruvate ...............................................23.2g
Use: For the isolation and cultivation of fastidious
Preparation of Sodium Pyruvate Solution:
and slow-growing, obligate anaerobic bacteria from a variety of clinical and nonclinical specimens. For the isolation and cultivation of Actinomyces israelii, Bacteroides melaninogenicus, Bacteroides thetaiotaomicron, Clostridium haemolyticum, and Fusobacterium necrophorum.
Add sodium pyruvate to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except sodium pyruvate solution, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Adjust pH to 7.3. Autoclave for 15 min at 15 psi pressure–121°C. Aseptically add 100.0mL of sterile sodium pyruvate solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation of Staphylococcus aureus.
CDC Anaerobe Blood Agar Composition per liter: Agar ..................................................................20.0g Pancreatic digest of casein................................15.0g Papaic digest of soybean meal ............................5.0g NaCl ....................................................................5.0g Yeast extract........................................................5.0g L-Cystine .............................................................0.4g Sheep blood, defibrinated ............................. 50.0mL
CDC Anaerobe Blood Agar with Kanamycin and Vancomycin Composition per liter: Agar ..................................................................20.0g Pancreatic digest of casein................................15.0g NaCl....................................................................5.0g Papaic digest of soybean meal............................5.0g Yeast extract........................................................5.0g L-Cystine .............................................................0.4g Sheep blood, defibrinated ............................. 50.0mL Antibiotic solution ........................................ 10.0mL Vitamin K1 solution ........................................ 1.0mL Hemin solution................................................ 0.5mL pH 7.5 ± 0.2 at 25°C
Source: This medium is available as a prepared medium from BD Diagnostic Systems.
CDC Anaerobe Laked Blood Agar with Kanamycin and Vancomycin
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Antibiotic Solution: Composition per 10.0mL:
Vitamin K1 Solution: Composition per 100.0mL:
Kanamycin ..........................................................0.1g Vancomycin .....................................................7.5mg
Vitamin K1 ..........................................................0.1g Phenylethyl alcohol ..........................................25.0g Ethanol.......................................................... 74.0mL
Preparation of Antibiotic Solution: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Vitamin K1 Solution: Composition per 100.0mL: Vitamin K1 ..........................................................1.0g Ethanol .......................................................... 99.0mL
Preparation of Vitamin K1 Solution: Add vitamin K1 to 99.0mL of absolute ethanol. Mix thoroughly. Filter sterilize.
Hemin Solution: Composition per 100.0mL: Hemin..................................................................1.0g NaOH (1N solution)...................................... 20.0mL
Preparation of Hemin Solution: Add hemin to 20.0mL of 1N NaOH solution. Mix thoroughly. Bring volume to 100.0mL with distilled/deionized water.
Preparation of Medium: Add components, except vitamin K1 solution and sheep blood, to distilled/deionized water and bring volume to 949.0mL. Mix thoroughly. Heat gently and bring to boiling for 1 min. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 50°–55°C. Aseptically add 1.0mL of sterile vitamin K1 solution and 50.0mL of sterile, defibrinated sheep blood. Mix thoroughly. Pour into sterile Petri dishes.
Use: For the selective isolation of fastidious and slow-growing, obligate anaerobic Gram-negative bacteria, especially Bacteroides species, from a variety of clinical and nonclinical specimens.
CDC Anaerobe Blood Agar with Phenylethyl Alcohol (CDC Anaerobe Blood Agar with PEA) Composition per liter: Agar ..................................................................20.0g Pancreatic digest of casein................................15.0g NaCl ....................................................................5.0g Papaic digest of soybean meal ............................5.0g Yeast extract........................................................5.0g L-Cystine .............................................................0.4g Sheep blood, defibrinated ............................. 50.0mL Vitamin K1 solution ...................................... 10.0mL Hemin solution................................................ 0.5mL pH 7.5 ± 0.2 at 25°C
Source: This medium is available as a prepared medium from BD Diagnostic Systems.
Preparation of Vitamin K1 Solution: Add components to 74.0mL of absolute ethanol. Mix thoroughly. Filter sterilize.
Hemin Solution: Composition per 100.0mL: Hemin .................................................................1.0g NaOH (1N solution)...................................... 20.0mL
Preparation of Hemin Solution: Add hemin to 20.0mL of 1N NaOH solution. Mix thoroughly. Bring volume to 100.0mL with distilled/deionized water.
Preparation of Medium: Add components, except vitamin K1 solution and sheep blood, to distilled/deionized water and bring volume to 940.0mL. Mix thoroughly. Heat gently and bring to boiling for 1 min. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 50°–55°C. Aseptically add 1.0mL of vitamin K1 solution and 50.0mL of sterile, defibrinated sheep blood. Mix thoroughly. Pour into sterile Petri dishes.
Use: For the selective isolation of fastidious and slow-growing, obligate anaerobic bacteria from a variety of clinical and nonclinical specimens.
CDC Anaerobe Laked Blood Agar with Kanamycin and Vancomycin (CDC Anaerobe Laked Blood Agar with KV) Composition per liter: Agar ..................................................................20.0g Pancreatic digest of casein................................15.0g Papaic digest of soybean meal............................5.0g Yeast extract........................................................5.0g L-Cystine .............................................................0.4g Sheep blood, defibrinated, laked .................. 50.0mL Antibiotic solution ........................................ 10.0mL Vitamin K1 solution ........................................ 1.0mL Hemin solution................................................ 0.5mL pH 7.5 ± 0.2 at 25°C
Source: This medium is available as a prepared medium from BD Diagnostic Systems.
Antibiotic Solution: Composition per 10.0mL: Kanamycin..........................................................0.1g Vancomycin .....................................................7.5mg
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Cefiximine Rhamnose Sorbitol MacConkey Agar
Preparation of Antibiotic Solution: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Vitamin K1 Solution: Composition per 100.0mL: Vitamin K1 ..........................................................1.0g Ethanol .......................................................... 99.0mL
Preparation of Vitamin K1 Solution: Add vita-
Selective Supplement Solution: Composition per 10.0mL: Cefiximine .....................................................0.05mg
Preparation of Selective Supplement Solution: Add cefiximine to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, ex-
Hemin..................................................................1.0g NaOH (1N solution)...................................... 20.0mL
cept selective supplement solution, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 50°C. Aseptially add selective supplement solution. Mix thoroughly. Pour into sterile Petri dishes.
Preparation of Hemin Solution: Add hemin to
Use: For the detection of Escherichia coli O157:H7.
min K1 to 99.0mL of absolute ethanol. Mix thoroughly. Filter sterilize.
Hemin Solution: Composition per 100.0mL:
20.0mL of 1N NaOH solution. Mix thoroughly. Bring volume to 100.0mL with distilled/deionized water.
Preparation of Medium: Add components, except antibiotic solution, vitamin K1, and laked sheep blood, to distilled/deionized water and bring volume to 939.0mL. Mix thoroughly. Heat gently and bring to boiling for 1 min. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Aseptically add the 1.0mL of sterile vitamin K1 solution and 10.0mL of sterile antibiotic solution. Mix thoroughly. Aseptically add 50.0mL of sterile, defibrinated, laked sheep blood. Laked blood is prepared by freezing whole blood overnight and thawing to room temperature. Mix thoroughly. Pour into sterile Petri dishes.
Use: For the selective isolation of fastidious and slow-growing, obligate anaerobic bacteria from a variety of clinical and nonclinical specimens.
Cefiximine Rhamnose Sorbitol MacConkey Agar (CR-SMAC Agar Base) Composition per liter: Peptone..............................................................20.0g Agar ..................................................................15.0g Sorbitol..............................................................10.0g NaCl ....................................................................5.0g Rhamnose............................................................5.0g Bile salts no. 3.....................................................1.5g Neutral Red .......................................................0.03g Crystal Violet ..................................................0.001g Selective supplement solution ...................... 10.0mL pH 7.1 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath.
This is selective, differential medium based on Sorbitol MacConkey Agar with added rhamnose and cefixime. This medium provides a selective base with improved differentiation of E. coli O157. The addition of rhamnose aids in the differentiation of Escherichia coli O157 from background flora. Cefixime reduces the level of competing flora, particularly Proteus spp., that often account for large numbers of non-sorbitol fermenting colonies E. coli O157 do not usually ferment sorbitol or rhamnose, so will appear as straw colored colonies. However, rhamnose is fermented by most sorbitol negative E. coli of other serogroups. These colonies will be pink/red and will not be counted as presumptive E. coli O157 colonies.
Cefsulodin Irgasan Novobiocin Agar (CIN Agar) (Yersinia Selective Agar) Composition per 1008.0mL: Basal medium ............................................. 757.0mL Desoxycholate solution............................... 200.0mL Cefsulodin solution....................................... 10.0mL Novobiocin solution...................................... 10.0mL Crystal Violet solution .................................. 10.0mL Strontium chloride solution .......................... 10.0mL Neutral Red solution ..................................... 10.0mL NaOH, 5N ....................................................... 1.0mL Irgasan solution............................................... 1.0mL pH 7.4 ± 0.2 at 25°C
Basal Medium: Composition per 757.0mL: Mannitol............................................................20.0g Special peptone.................................................20.0g Agar ..................................................................12.0g Sodium pyruvate.................................................2.0g Yeast extract........................................................2.0g
Cell Growth Medium NaCl ....................................................................1.0g Magnesium sulfate solution ............................ 1.0mL
Preparation of Basal Medium: Add compo-
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Preparation of Novobiocin Solution: Add novobiocin to 10.0mL of distilled/deionized water. Mix thoroughly. Filter sterilize.
nents to distilled/deionized water and bring volume to 757.0mL. Mix thoroughly. Gently heat and bring to boiling with stirring. Cool to about 80°C by placing in a 50°C water bath for about 10 min.
Strontium Chloride Solution: Composition per 10.0mL:
Magnesium Sulfate Solution: Composition per 10mL:
tium chloride to 10.0mL of distilled/deionized water. Mix thoroughly. Filter sterilize.
MgSO4·7H2O ......................................................0.1g
Preparation of Magnesium Sulfate Solution: Add MgSO4·7H2O to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly.
Irgasan Solution: Composition per 10mL: Irgasan (triclosan) .............................................0.04g
Preparation of Irgasan Solution: Add irgasan to 95% ethanol and bring volume to 10.0mL. Mix thoroughly. Can be stored for 4 weeks at –20°C.
Desoxycholate Solution: Composition per 200.0mL: Na-desoxycholate................................................0.5g
Preparation of Desoxycholate Solution: Add desoxycholate to distilled/deionized water and bring volume to 200.0mL. Mix thoroughly. Gently heat and bring to boiling with stirring. Cool to 50–55°C.
Neutral Red Solution: Composition per 10.0mL: Neutral Red ....................................................30.0mg
Preparation of Neutral Red Solution: Add Neutral Red to 10.0mL of distilled/deionized water. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C.
Crystal Violet Solution: Composition per 10.0mL: Crystal Violet ...................................................1.0mg
Preparation of Crystal Violet Solution: Add Crystal Violet to 10.0mL of distilled/deionized water. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C.
Cefsulodin Solution: Composition per 10.0mL: Cefsulodin......................................................15.0mg
Preparation of Cefsulodin Solution: Add cefsulodin to 10.0mL of distilled/deionized water. Mix thoroughly. Filter sterilize.
Novobiocin Solution: Composition per 10.0mL: Novobiocin.......................................................2.5mg
SrCl2·6H2O .........................................................1.0g
Preparation of Strontium Chloride: Add stron-
Preparation of Medium: Add 1.0mL irgasan solution to 757.0mL basal medium. Mix thoroughly. Cool to 50–55°C. Add 200.0mL desoxychlolate solution. Mix thoroughly. Solution should remain clear. Aseptically add 1.0mL 5N NaOH, 10.0mL Neutral Red solution, 10.0mL Crystal Violet solution, 10.0mL cefsulodin solution, and 10.0mL novobiocin solution. Mix thoroughly. Slowly add 10.0mL strontium chloride solution while continuously stirring. Adjust pH to 7.4 with 5N NaOH. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the selective isolation and differentiation of Yersinia enterocolitica based on mannitol fermentation. Yersinia enterocolitica appears as “bull’s eye” colonies with deep red centers surrounded by a transparent periphery.
Cell Growth Medium Composition per 2250.0mL: Eagle’s minimal essential medium with Hanks’ salts (MEMH) ......................... 1.0L L 15 medium, modified Leibovitz ..................... 1.0L Fetal calf serum........................................... 200.0mL NaHCO3 solution .......................................... 50.0mL pH 7.5 at 25°C
MEMH: Composition per liter: NaCl....................................................................8.0g Glucose ...............................................................1.0g KCl......................................................................0.4g CaCl2·2H2O ......................................................0.14g MgSO4·7H2O ......................................................0.1g KH2PO4.............................................................0.06g Na2HPO4 ...........................................................0.05g L-Isoleucine .....................................................0.026g L-Leucine ........................................................0.026g L-Lysine...........................................................0.026g L-Threonine .....................................................0.024g L-Valine .........................................................0.0235g L-Tyrosine .......................................................0.018g L-Arginine .....................................................0.0174g L-Phenylalanine.............................................0.0165g L-Cystine .........................................................0.012g L-Histidine........................................................8.0mg
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Cellobiose Polymyxin B Colistin Agar, Modified
L-Methionine ....................................................7.5mg
Phenol Red.......................................................5.0mg L-Tryptophan ....................................................4.0mg Inositol .............................................................1.8mg Biotin ...............................................................1.0mg Folic acid..........................................................1.0mg Calcium pantothenate ......................................1.0mg Choline chloride...............................................1.0mg Nicotinamide....................................................1.0mg Pyridoxal·HCl ..................................................1.0mg Thiamine·HCl ..................................................1.0mg Riboflavin ........................................................0.1mg
Preparation of MEMH: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
L 15 Medium, Modified Leibovitz: Composition per liter: NaCl ....................................................................8.0g DL-Threonine.......................................................0.6g Sodium pyruvate .................................................0.6g DL-Alanine...........................................................0.5g L-Arginine, free base ...........................................0.5g KCl......................................................................0.4g L-Asparagine·H2O ...............................................0.3g L-Histidine, free base...........................................0.3g L-Glutamine.........................................................0.3g L-Isoleucine .........................................................0.3g L-Phenylalanine...................................................0.3g L-Tyrosine............................................................0.3g DL-Methionine.....................................................0.2g DL-Valine .............................................................0.2g Glycine................................................................0.2g L-Serine ...............................................................0.2g Na2HPO4, anhydrous ..........................................0.2g CaCl2, anhydrous ................................................0.1g L-Cysteine, free base ...........................................0.1g L-Leucine·HCl .....................................................0.1g Streptomycin .......................................................0.1g MgCl2, anhydrous ...........................................0.094g D-Galactose .......................................................0.09g KH2PO4 .............................................................0.06g Gentamicin........................................................0.05g L-Tryptophan .....................................................0.02g Phenol Red........................................................0.01g i-Inositol...........................................................2.0mg Choline chloride...............................................1.0mg D-Calcium pantothenate ...................................1.0mg Folic acid..........................................................1.0mg Nicotinamide....................................................1.0mg Pyridoxine·HCl ................................................1.0mg Thiamine monophosphate·2H2O......................1.0mg Riboflavin-5-phosphate ...................................0.1mg Penicillin G ................................................100,000U pH 7.5 ± 0.2 at 25°C
Preparation of L 15 Medium, Modified Leibovitz: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize. Store at 5°C.
NaHCO3 Solution: Composition per 100.0mL: NaHCO3 ..............................................................7.5g
Preparation of NaHCO3 Solution: Add NaHCO3 to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Aseptically combine 1.0L of sterile Eagle’s minimal essential medium with Hanks’ salts (MEMH) and 1.0L of sterile L 15 medium, modified Leibovitz. Mix thoroughly. Immediately prior to use, aseptically add 200.0mL of fetal calf serum and 50.0mL of NaHCO3 solution. Mix thoroughly. Aseptically distribute into sterile containers.
Use: For the cultivation of mammalian HeLa or Vero tissue culture cells to test the cytopathic effects of Escherichia coli.
Cellobiose Polymyxin B Colistin Agar, Modified Composition per liter: Solution 1.................................................... 900.0mL Solution 2.................................................... 100.0mL pH 7.6 ± 0.2 at 25°C
Solution 1: Composition per 900.0mL: NaCl..................................................................20.0g Agar ..................................................................15.0g Peptone .............................................................10.0g Beef extract.........................................................5.0g 1000× dye stock solution ................................ 1.0mL
Preparation of Solution 1: Add components to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Adjust pH to 7.6. Gently heat and bring to boiling. Do not autoclave. Cool to 48°–55°C.
1000X Dye Stock Solution: Composition per 100.0mL: Bromthymol Blue ...............................................4.0g Cresol Red ..........................................................4.0g Ethanol (95% solution) ............................... 100.0mL
Preparation of 1000X Dye Stock Solution: Add Bromthymol Blue and Cresol Red to 100.0mL of ethanol. Mix thoroughly.
Solution 2: Composition per 100.0mL: Cellobiose .........................................................10.0g
CF Assay Medium Colistin.......................................................400,000U Polymyxin B ..............................................100,000U
Preparation of Solution 2: Add cellobiose to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Gently heat until dissolved. Cool to 25°C. Add colistin and polymyxin B. Mix thoroughly.
Preparation of Medium: Combine cooled solution 1 and solution 2. Mix thoroughly. Do not autoclave. Pour into sterile Petri dishes.
Use: For the cultivation of Vibrio species.
Cellobiose Polymyxin Colistin Agar (CPC Agar) Composition per liter: Solution A ................................................... 900.0mL Solution B ................................................... 100.0mL pH 7.6 ± 0.2 at 25°C
Solution A: Composition per 900.0mL: NaCl ..................................................................20.0g Agar ..................................................................15.0g Peptone..............................................................10.0g Beef extract .........................................................5.0g Bromthymol Blue .............................................0.04g Cresol Red.........................................................0.04g
Preparation of Solution A: Add components to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Adjust pH to 7.6. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C.
Solution B: Composition per 100.0mL: Cellobiose .........................................................15.0g Colistin....................................................1,360,000U Polymyxin B ..............................................100,000U
Preparation of Solution B: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Aseptically combine 900.0mL of cooled, sterile solution A and 100.0mL of sterile solution B. Mix thoroughly. Pour into sterile Petri dishes. Use within 7 days. Use: For the cultivation and identification of Vibrio species.
Cereal Agar Composition per liter: Cereal, precooked mixed ................................100.0g Agar ..................................................................15.0g
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Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or distribute into sterile tubes. Allow tubes to cool in a slanted position.
Use: For the cultivation and sporulation of fungi.
Cetrimide Agar, Non-USP Composition per liter: Beef heart, solids from infusion......................500.0g Agar ..................................................................15.0g Tryptose ............................................................10.0g NaCl....................................................................5.0g Cetrimide ............................................................0.9g pH 7.2 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 13 psi pressure–118°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the selective isolation, cultivation, and identification of Pseudomonas aeruginosa and other Gram-negative, nonfermentative bacteria.
Cetrimide Agar, USP (Pseudosel® Agar) Composition per liter: Pancreatic digest of gelatin...............................20.0g Agar ..................................................................13.6g K2SO4 ...............................................................10.0g MgCl2..................................................................1.4g Cetrimide ............................................................0.3g Glycerol ........................................................ 10.0mL pH 7.2 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 13 psi pressure–118°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the selective isolation, cultivation, and identification of Pseudomonas aeruginosa and other Gram-negative, nonfermentative bacteria.
CF Assay Medium (Citrovorum Factor Assay Medium) Composition per liter: Glucose .............................................................50.0g
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CFAT Medium
Sodium acetate..................................................40.0g Vitamin assay casamino acids...........................10.0g NH4Cl .................................................................6.0g K2HPO4 ...............................................................1.2g KH2PO4 ...............................................................1.2g MgSO4·7H2O ......................................................0.4g DL-Alanine...........................................................0.2g DL-Tryptophan.....................................................0.2g L-Cystine .............................................................0.2g L-Cysteine·HCl....................................................0.2g MgSO4·7H2O ....................................................0.04g Adenine sulfate .................................................0.02g FeSO4 ................................................................0.02g Glycine..............................................................0.02g Guanine·HCl .....................................................0.02g NaCl ..................................................................0.02g Uracil ................................................................0.02g Xanthine............................................................0.02g Pyridoxamine·HCl ...........................................6.0mg Nicotinic acid ...................................................2.0mg Pyridoxine·HCl ................................................2.0mg Calcium pantothenate ......................................1.0mg Riboflavin ........................................................1.0mg Thiamine·HCl ..................................................1.0mg Pyridoxal·HCl .............................................. 600.0µg p-Aminobenzoic acid................................... 200.0µg Folic acid........................................................ 20.0µg Biotin ............................................................... 2.0µg pH 6.7 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Continue boiling for 2–3 min. Allow precipitate to settle out. Distribute supernatant into tubes in 5.0mL volumes. Add standard solution or test solutions to each tube. Adjust the volume of each tube to 10.0mL with distilled/deionized water. Autoclave for 10 min at 15 psi pressure–121°C.
Use: For the microbiological assay of citrovorum factor using Pediococcus acidilactici.
CFAT Medium (Cadmium Fluoride Acriflavin Tellurite Medium) Composition per liter: Pancreatic digest of casein................................17.0g Agar ..................................................................15.0g Glucose ...............................................................7.5g NaCl ....................................................................5.0g Papaic digest of soybean meal ............................3.0g K2HPO4 ...............................................................2.5g NaF......................................................................0.8g CdSO4 .............................................................0.013g K2TeO3 .............................................................2.5mg
Neutral acriflavin .............................................1.2mg Basic Fuchsin.................................................0.25mg Sheep blood, defibrinated ............................. 50.0mL
Caution: Potassium tellurite is toxic. Preparation of Medium: Add components, except sheep blood, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Add 50.0mL of sterile, defibrinated sheep blood. Mix thoroughly. Pour into sterile Petri dishes or leave in tubes.
Use: For the isolation, cultivation, and enumeration of Actinomyces viscosus and Actinomyces naeslundii from clinical specimens, especially dental plaque.
CGY Agar Composition per liter: Agar ..................................................................20.0g Pancreatic digest of casein..................................5.0g Yeast extract........................................................1.0g Glycerol ........................................................ 10.0mL pH 7.2 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of Bacillus pseudogordonae.
CH 1 Medium Composition per liter: NaCl................................................................250.0g Tris(hydroxymethyl)amino methane buffer............................................12.0g Glycerol ............................................................10.0g Hy-Case SF.........................................................5.0g Yeast extract........................................................5.0g Solution 1...................................................... 50.0mL
Solution 1: Composition per liter: MgCl2·6H2O .....................................................40.0g KCl......................................................................4.0g CaCl2·2H2O ........................................................0.4g pH 7.4 ± 0.2 at 25°C
Preparation of Solution 1: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix
Charcoal Agar with Horse Blood and Cepahalexin thoroughly. Adjust pH to 7.4. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of Haloarcula vallismortis.
Chapman Stone Agar Composition per liter: (NH4)2SO4.........................................................75.0g NaCl ..................................................................55.0g Gelatin...............................................................30.0g Agar ..................................................................15.0g D-Mannitol ........................................................10.0g Pancreatic digest of casein................................10.0g K2HPO4 ...............................................................5.0g Yeast extract........................................................2.0g pH 7.0 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Autoclave for 10 min at 15 psi pressure–121°C. Pour into sterile Petri dishes while the medium is still hot. Add 25.0mL of medium per Petri dish.
Use: For the isolation of staphylococci from a variety of specimens.
Charcoal Agar Composition per liter: Beef heart, solids from infusion......................500.0g Agar ..................................................................18.0g Peptone..............................................................10.0g Soluble starch....................................................10.0g NaCl ....................................................................5.0g Charcoal, activated, acid washed........................4.0g Yeast extract........................................................3.5g pH 7.3 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling with frequent stirring. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Pour into sterile Petri dishes or leave in tubes. Shake flask while dispensing to keep charcoal in suspension. Allow tubes to cool in a slanted position.
Use: For the cultivation and maintenance of fastidious microorganisms.
Charcoal Agar Composition per liter: Agar ..................................................................12.0g
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Beef extract.......................................................10.0g Peptone .............................................................10.0g Starch ................................................................10.0g NaCl....................................................................5.0g Charcoal..............................................................4.0g Nicotinic acid..................................................0.001g pH 7.4 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling with frequent stirring. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. This medium may be enriched by the addition of blood. Pour into sterile Petri dishes or distribute into tubes. Shake flask while dispensing to keep charcoal in suspension.
Use: For the cultivation and isolation of various bacteria; with the addition of blood, for the cultivation of fastidious bacteria.
Charcoal Agar with Horse Blood Composition per liter: Agar ..................................................................12.0g Beef extract.......................................................10.0g Peptone .............................................................10.0g Starch ................................................................10.0g NaCl....................................................................5.0g Charcoal, bacteriological ....................................4.0g Nicotinic acid...................................................1.0mg Horse blood, defibrinated ........................... 100.0mL pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 900.0L. Mix thoroughly. Gently heat and bring to boiling with frequent stirring. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 80°C. Aseptically add 100.0mL of sterile, defibrinated horse blood. Maintain at 80°C for 10 min to form chocolate agar. Pour into sterile Petri dishes or distribute into tubes. Shake flask while dispensing to keep charcoal in suspension.
Use: For the cultivation and isolation of Haemophilus influenzae.
Charcoal Agar with Horse Blood and Cepahalexin Composition per liter: Agar ..................................................................12.0g Beef extract.......................................................10.0g Peptone .............................................................10.0g Starch ................................................................10.0g
126
Charcoal Blood Medium
NaCl ....................................................................5.0g Charcoal ..............................................................4.0g Nicotinic acid ...................................................1.0mg Horse blood, defibrinated ........................... 100.0mL Cephalexin solution ...................................... 10.0mL pH 7.4 ± 0.2 at 25°C
Cephalexin Solution: Composition per 10.0mL: Cephalexin ........................................................0.04g
Preparation of Cephalexin Solution: Add cephalexin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. Preparation of Medium: Add components, except cephalexin solution and horse blood, to distilled/ deionized water and bring volume to 890.0L. Mix thoroughly. Gently heat and bring to boiling with frequent stirring. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 100.0mL of sterile, defibrinated horse blood and 10.0mL of sterile cephalexin solution. Pour into sterile Petri dishes or distribute into tubes. Shake flask while dispensing to keep charcoal in suspension.
Use: For the cultivation and isolation of Bordetella pertussis.
Charcoal Blood Medium Composition per liter: Beef heart, solids from infusion......................500.0g Agar ..................................................................18.0g Peptone..............................................................10.0g Soluble starch....................................................10.0g NaCl ....................................................................5.0g Charcoal, activated, acid washed........................4.0g Yeast extract........................................................3.5g Horse or sheep blood, defibrinated ............. 100.0mL Cephalexin solution ...................................... 10.0mL pH 7.4 ± 0.2 at 25°C
Cephalexin Solution: Composition per 10.0mL: Cephalexin ........................................................0.04g
Preparation of Cephalexin Solution: Add cephalexin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. Preparation of Medium: Add components, except blood and cephalexin solution, to distilled/ deionized water and bring volume to 890.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile blood and cephalexin solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation of Haemophilus influenzae.
Chlamydia Growth Medium Composition per 500.0mL: Eagle minimum essential medium with Earle salts, 10X .............................. 50.0mL Fetal calf serum............................................. 50.0mL L-Glutamine solution....................................... 5.0mL pH 7.4 ± 0.2 at 25°C
Eagle Minimum Essential Medium with Earle Salts, 10X: Composition per liter: NaCl....................................................................6.8g Glucose ...............................................................1.0g KCl......................................................................0.4g CaCl2·2H2O ........................................................0.2g MgCl2·6H2O .......................................................0.2g NaH2PO4 ...........................................................0.15g L-Arginine ...........................................................0.1g L-Lysine.............................................................0.06g L-Isoleucine .......................................................0.05g L-Leucine ..........................................................0.05g L-Threonine .......................................................0.05g L-Valine .............................................................0.05g L-Tyrosine .........................................................0.04g L-Phenylalanine.................................................0.03g L-Histidine.........................................................0.03g L-Cystine ...........................................................0.02g L-Methionine .....................................................0.02g L-Tryptophan.....................................................0.01g i-Inositol...........................................................2.0mg Calcium pantothenate ......................................1.0mg Choline chloride...............................................1.0mg Folic acid .........................................................1.0mg Nicotinamide....................................................1.0mg Pyridoxal..........................................................1.0mg Thiamine·HCl ..................................................1.0mg Riboflavin ........................................................0.1mg
Preparation of Eagle Minimum Essential Medium With Earle Salts, 10X: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.4 with 7.5% Na2CO3 solution. Filter sterilize.
Glutamine Solution: Composition per 100.0mL: L-Glutamine
......................................................2.92g NaCl (0.85% solution) ................................ 100.0mL
Preparation of Glutamine Solution: Add the glutamine to the 0.85% NaCl solution. Mix thoroughly. Filter sterilize.
Preparation of Medium: Aseptically combine 50.0mL of sterile Eagle minimum essential mediumwith Earle salts, 10X, 50.0mL of fetal calf serum, and 5.0mL of sterile glutamine solution. Bring volume to 500.0mL with sterile distilled/deionized water. Mix
Chloramphenicol Ampicillin LB Medium thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation of Chlamydia species.
Chlamydia Isolation Medium Composition per 500.0mL: Eagle minimum essential medium with Earle salts, 10X .............................. 50.0mL Fetal calf serum............................................. 50.0mL Selective supplement .................................... 10.0mL L-Glutamine solution....................................... 5.0mL pH 7.4 ± 0.2 at 25°C
Eagle Minimum Essential Medium with Earle Salts, 10X: Composition per liter: NaCl ....................................................................6.8g Glucose ...............................................................1.0g KCl......................................................................0.4g CaCl2·2H2O.........................................................0.2g MgCl2·6H2O .......................................................0.2g NaH2PO4 ...........................................................0.15g L-Arginine ...........................................................0.1g L-Lysine.............................................................0.06g L-Isoleucine .......................................................0.05g L-Leucine...........................................................0.05g L-Threonine .......................................................0.05g L-Valine .............................................................0.05g L-Tyrosine..........................................................0.04g L-Phenylalanine.................................................0.03g L-Histidine.........................................................0.03g L-Cystine ...........................................................0.02g L-Methionine .....................................................0.02g L-Tryptophan .....................................................0.01g i-Inositol...........................................................2.0mg Calcium pantothenate ......................................1.0mg Choline chloride...............................................1.0mg Folic acid..........................................................1.0mg Nicotinamide....................................................1.0mg Pyridoxal..........................................................1.0mg Thiamine·HCl ..................................................1.0mg Riboflavin ........................................................0.1mg
Preparation of Eagle Minimum Essential Medium With Earle Salts, 10X: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.4 with 7.5% Na2CO3 solution. Filter sterilize.
Selective Supplement: Composition per 10.0mL: Glucose ...........................................................0.594g Vancomycin ......................................................0.05g Gentamicin........................................................0.01g Amphotericin B................................................2.0mg Cycloheximide .................................................2.0mg
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Preparation of Selective Supplement: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Glutamine Solution: Composition per 100.0mL: L-Glutamine
......................................................2.92g NaCl (0.85% solution) ................................ 100.0mL
Preparation of Glutamine Solution: Add the glutamine to the 0.85% NaCl solution. Mix thoroughly. Filter sterilize.
Preparation of Medium: Aseptically combine 50.0mL of sterile Eagle minimum essential medium with Earle salts, 10X, 50.0mL of fetal calf serum, 10.0mL of selective supplement, and 5.0mL of sterile glutamine solution. Bring volume to 500.0mL with sterile distilled/deionized water. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the isolation and cultivation of Chlamydia species.
Chlamydospore Agar Composition per liter: Purified polysaccharide ....................................20.0g Agar ..................................................................15.0g KH2PO4...............................................................1.0g (NH4)2SO4 ..........................................................1.0g Trypan Blue ........................................................0.1g Biotin ................................................................5.0µg pH 5.1 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For differentiating Candida albicans from other Candida species on the basis of chlamydospore formation.
Chloramphenicol Ampicillin LB Medium Composition per liter: NaCl..................................................................10.0g Pancreatic digest of casein................................10.0g Yeast extract........................................................5.0g Ampicillin solution ....................................... 10.0mL Chloramphenicol solution............................. 10.0mL pH 7.0 ± 0.2 at 25°C
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Chloramphenicol Erythromycin LB Medium
Ampicillin Solution: Composition per 10.0mL: Ampicillin ......................................................40.0mg
Preparation of Ampicillin Solution: Add ampicillin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Chloramphenicol Solution: Composition per 10.0mL:
clave for 15 min at 15 psi pressure–121°C. Aseptically add 10.0mL of sterile ampicillin solution and 10.0mL of sterile chloramphenicol solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation and maintenance of Escherichia coli.
Chloramphenicol L Broth Medium No. 1
Chloramphenicol..............................................5.0mg
Composition per liter:
Preparation of Chloramphenicol Solution:
Pancreatic digest of casein................................10.0g NaCl....................................................................5.0g Yeast extract........................................................5.0g Glucose ...............................................................1.0g Chloramphenicol........................................... 10.0mL pH 7.0 ± 0.2 at 25°C
Add chloramphenicol to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except ampicillin solution and chloramphenicol solution, to distilled/deionized water and bring volume to 980.0mL. Mix thoroughly. Adjust pH to 7.0. Autoclave for 15 min at 15 psi pressure–121°C. Aseptically add 10.0mL of sterile ampicillin solution and 10.0mL of sterile chloramphenicol solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation and maintenance of Escherichia coli.
Chloramphenicol Erythromycin LB Medium Composition per liter: NaCl ..................................................................10.0g Pancreatic digest of casein................................10.0g Yeast extract........................................................5.0g Erythromycin ................................................ 10.0mL Chloramphenicol........................................... 10.0mL pH 7.0 ± 0.2 at 25°C
Erythromycin Solution: Composition per 10.0mL: Erythromycin ....................................................10mg
Preparation of Erythromycin Solution: Add erythromycin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. Chloramphenicol Solution: Composition per 10.0mL: Chloramphenicol..............................................5.0mg
Preparation of Chloramphenicol Solution: Add chloramphenicol to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except erythromycin solution and chloramphenicol solution, to distilled/deionized water and bring volume to 980.0mL. Mix thoroughly. Adjust pH to 7.0. Auto-
Chloramphenicol Solution: Composition per 10.0mL: Chloramphenicol..............................................5.0mg
Preparation of Chloramphenicol Solution: Add chloramphenicol to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except chloramphenicol solution, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Adjust pH to 7.0. Autoclave for 15 min at 15 psi pressure–121°C. Aseptically add 10.0mL of sterile ampicillin solution and 10.0mL of sterile chloramphenicol solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation and maintenance of Escherichia coli.
Chloramphenicol L Broth Medium No. 2 Composition per liter: Pancreatic digest of casein................................10.0g NaCl....................................................................5.0g Yeast extract........................................................5.0g Glucose ...............................................................1.0g Chloramphenicol........................................... 10.0mL pH 7.0 ± 0.2 at 25°C
Chloramphenicol Solution: Composition per 10.0mL: Chloramphenicol............................................12.5mg
Preparation of Chloramphenicol Solution: Add chloramphenicol to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except chloramphenicol solution, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly.
Chocolate Agar
129
Adjust pH to 7.0. Autoclave for 15 min at 15 psi pressure–121°C. Aseptically add 10.0mL of sterile ampicillin solution and 10.0mL of sterile chloramphenicol solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Yeast extract........................................................5.0g Chloramphenicol........................................... 10.0mL pH 7.0 ± 0.2 at 25°C
Use: For the cultivation and maintenance of Escher-
Chloramphenicol..............................................5.0mg
ichia coli.
Chloramphenicol L Broth Medium No. 3 Composition per liter: Pancreatic digest of casein................................10.0g NaCl ....................................................................5.0g Yeast extract........................................................5.0g Glucose ...............................................................1.0g Chloramphenicol........................................... 10.0mL pH 7.0 ± 0.2 at 25°C
Chloramphenicol Solution: Composition per 10.0mL: Chloramphenicol............................................50.0mg
Preparation of Chloramphenicol Solution: Add chloramphenicol to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except chloramphenicol solution, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Adjust pH to 7.0. Autoclave for 15 min at 15 psi pressure–121°C. Aseptically add 10.0mL of sterile ampicillin solution and 10.0mL of sterile chloramphenicol solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation and maintenance of Escherichia coli.
Chloramphenicol LB Medium No.1 Composition per liter: NaCl ..................................................................10.0g Pancreatic digest of casein................................10.0g Yeast extract........................................................5.0g Chloramphenicol............................................ 50.0µg
Preparation of Medium: Adjust pH to 7.0. Autoclave at 15 psi pressure–121°C for 15 min. For solid medium, add 15.0g of agar.
Use: For the cultivation of and maintenance of Escherichia coli.
Chloramphenicol LB Medium No. 2 Composition per liter: NaCl ..................................................................10.0g Pancreatic digest of casein................................10.0g
Chloramphenicol Solution: Composition per 10.0mL: Preparation of Chloramphenicol Solution: Add chloramphenicol to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except chloramphenicol solution, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Adjust pH to 7.0. Autoclave for 15 min at 15 psi pressure–121°C. Aseptically add 10.0mL of sterile ampicillin solution and 10.0mL of sterile chloramphenicol solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation and maintenance of Escherichia coli.
CHO Medium Base (Carbohydrate Medium Base) Composition per liter: Pancreatic digest of casein................................15.0g Yeast extract........................................................7.0g NaCl....................................................................2.5g Agar ..................................................................0.75g Sodium thioglycolate ..........................................0.5g L-Cystine ...........................................................0.25g Ascorbic acid ......................................................0.1g Bromthymol Blue .............................................0.01g pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Use: Used as a basal medium to which carbohydrates are added for fermentation studies of anaerobic bacteria. Generally, 6.25mL of a 10% filter-sterilized solution of carbohydrate is added to the sterile basal medium.
Chocolate Agar Composition per liter: Agar ..................................................................15.0g Pantone .............................................................10.0g Bitone................................................................10.0g NaCl....................................................................5.0g Tryptic digest of beef heart.................................3.0g Cornstarch...........................................................1.0g
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Chocolate Agar
Sheep blood, defibrinated ........................... 100.0mL Supplement B................................................ 10.0mL pH 7.3 ± 0.2 at 25°C
Hemoglobin Solution: Composition per 100.0mL:
Supplement B: Composition per 10.0mL:
Preparation of Hemoglobin Solution: Add he-
Cephalothin....................................................15.0mg Vancomycin ...................................................10.0mg Trimethoprim ...................................................5.0mg Amphotericin B................................................2.0mg Polymyxin B ...................................................2500U
Preparation of Medium: Add components, ex-
Preparation of Supplement B: Add components to 10.0mL of distilled/deionized water. Mix thoroughly. Filter sterilize.
Source: Supplemement B is available from BD Diagnostic Systems.
Preparation of Medium: Add components, except hemoglobin solution and sheep blood, to distilled/deionized water and bring volume to 890.0mL. Mix thoroughly. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°– 50°C. Aseptically add 100.0mL of sterile, defibrinated sheep blood. Gently heat while stirring and bring to 85°C for 5–10 min. Cool to 50°C. Aseptically add 10.0mL of sterile supplement B. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation and cultivation of a variety of fastidious microorganisms.
Hemoglobin ......................................................10.0g moglobin to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize. cept hemoglobin solution and supplement B, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 100.0mL of sterile hemoglobin solution. Gently heat while stirring and bring to 85°C for 5–10 min. Cool to 50°C. Aseptically add 10.0mL of sterile supplement B. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation and cultivation of fastidious microorganisms.
Chocolate Agar, Enriched Composition per liter: GC medium base......................................... 740.0mL Hemoglobin solution .................................. 250.0mL Supplement B................................................ 10.0mL pH 7.3 ± 0.2 at 25°C
Source: This medium is available from BD Diagnostic Systems.
Chocolate Agar Composition per liter: Proteose peptone no. 3 ......................................15.0g Agar ..................................................................10.0g NaCl ....................................................................5.0g K2HPO4 ...............................................................4.0g Cornstarch...........................................................1.0g KH2PO4 ...............................................................1.0g Hemoglobin solution................................... 100.0mL Supplement B................................................ 10.0mL pH 7.0 ± 0.2 at 25°C
Source: This medium is available from BD Diagnostic Systems.
Supplement B: Composition per 10.0mL: Cephalothin....................................................15.0mg Vancomycin ...................................................10.0mg Trimethoprim ...................................................5.0mg Amphotericin B................................................2.0mg Polymyxin B ...................................................2500U
Preparation of Supplement B: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
GC Medium Base: Composition per 740.0mL: Agar ..................................................................20.0g Proteose peptone no. 3......................................15.0g NaCl....................................................................5.0g K2HPO4...............................................................4.0g Glucose ...............................................................1.5g Cornstarch...........................................................1.0g KH2PO4...............................................................1.0g pH 7.2 ± 0.2 at 25°C
Preparation of GC Medium Base: Add components to distilled/deionized water and bring volume to 740.0mL. Mix thoroughly. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Hemoglobin Solution: Composition per 250.0mL: Hemoglobin ......................................................10.0g
Preparation of Hemoglobin Solution: Add hemoglobin to distilled/deionized water and bring volume to 250.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Chocolate Agar-Bartonella C-29 Supplement B: Composition per 10.0mL: Cephalothin....................................................15.0mg Vancomycin ...................................................10.0mg Trimethoprim ...................................................5.0mg Amphotericin B................................................2.0mg Polymyxin B ...................................................2500U
Preparation of Supplement B: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. Preparation of Medium: To 740.0mL of cooled sterile GC medium base, aseptically add 250.0mL of sterile hemoglobin solution and 10.0mL of sterile supplement B. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes. Use: For the cultivation of fastidious microorganisms, especially Neisseria species.
Chocolate Agar, Enriched Composition per liter: GC medium base......................................... 740.0mL Hemoglobin solution................................... 250.0mL Supplement VX............................................. 10.0mL pH 7.3 ± 0.2 at 25°C
Source: This medium is available from BD Diagnostic Systems.
GC Medium Base: Composition per 740.0mL: Agar ..................................................................20.0g Proteose peptone no. 3 ......................................15.0g NaCl ....................................................................5.0g K2HPO4 ...............................................................4.0g Glucose ...............................................................1.5g Cornstarch...........................................................1.0g KH2PO4 ...............................................................1.0g pH 7.2 ± 0.2 at 25°C
Preparation of GC Medium Base: Add components to distilled/deionized water and bring volume to 740.0mL. Mix thoroughly. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Hemoglobin Solution: Composition per 250.0mL: Hemoglobin ......................................................10.0g
131
Preparation of Supplement VX: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: To 740.0mL of cooled sterile GC medium base, aseptically add 250.0mL of sterile hemoglobin solution and 10.0mL of sterile supplement B. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes. Use: For the cultivation of fastidious microorganisms, especially Neisseria species.
Chocolate Agar-Bartonella C-29 (ATCC Medium 2119) Composition per 1010.0mL: GC agar base solution..................................500.0 ml Hemoglobin solution ...................................500.0 ml IsoVitaleX® enrichment ............................... 10.0mL
IsoVitaleX Enrichment: Composition per liter: Glucose ...........................................................100.0g L-Cysteine·HCl..................................................25.9g L-Glutamine ......................................................10.0g L-Cystine .............................................................1.1g Adenine...............................................................1.0g Nicotinamide adenine dinucleotide ..................0.25g Vitamin B12 .........................................................0.1g Thiamine pyrophosphate ....................................0.1g Guanine·HCl .....................................................0.03g Fe(NO3)3·6H2O.................................................0.02g p-Aminobenzoic acid......................................0.013g Thiamine·HCl ..................................................3.0mg
Preparation of IsoVitaleX: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
GC Agar Base Solution: Composition per 500.0mL: Agar ..................................................................10.0g Pancreatic digest of casein..................................7.5g Peptic digest of animal tissue .............................7.5g NaCl....................................................................5.0g K2HPO4...............................................................4.0g Cornstarch...........................................................1.0g KH2PO4...............................................................1.0g
moglobin to distilled/deionized water and bring volume to 250.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Preparation of GC Agar Base: Add components to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Supplement VX: Composition per 10.0mL:
Hemoglobin Solution: Composition per 500.0mL:
Supplement VX contains essential growth factors.
Hemoglobin ......................................................10.0g
Preparation of Hemoglobin Solution: Add he-
132
Chocolate II Agar
Preparation of Hemoglobin Solution: Add hemoglobin to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C.
Preparation of Medium: Aseptically combine 500.0mL sterile, cooled GC agar base solution, and 500.0mL cooled sterile hemoglobin solution. Aseptically add 10.0mL of sterile IsoVitaleX enrichment. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes. Use: For the isolation and cultivation of fastidious microorganisms, especially Neisseria and Haemophilus species, from a variety of clinical specimens.
Chocolate II Agar Composition per liter: Agar ..................................................................12.0g Hemoglobin ......................................................10.0g Pancreatic digest of casein..................................7.5g Selected meat peptone ........................................7.5g NaCl ....................................................................5.0g K2HPO4 ...............................................................4.0g Cornstarch...........................................................1.0g KH2PO4 ...............................................................1.0g
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the isolation and cultivation of fastidious microorganisms.
Chocolate II Agar with Hemoglobin and IsoVitaleX (GCII Agar with Hemoglobin and IsoVitaleX) Composition per liter: GCII agar base ............................................ 990.0mL IsoVitaleX enrichment .................................. 10.0mL pH 7.3 ± 0.2 at 25°C
Source: This medium is available as a prepared medium from BD Diagnostic Systems.
GCII Agar Base: Composition per liter: Agar ..................................................................12.0g Hemoglobin ......................................................10.0g Pancreatic digest of casein..................................7.5g Selected meat peptone ........................................7.5g NaCl ....................................................................5.0g K2HPO4 ...............................................................4.0g
Cornstarch...........................................................1.0g KH2PO4...............................................................1.0g
Preparation of GCII Agar Base: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
IsoVitaleX Enrichment: Composition per liter: Glucose ...........................................................100.0g L-Cysteine·HCl..................................................25.9g L-Glutamine ......................................................10.0g L-Cystine .............................................................1.1g Adenine...............................................................1.0g Nicotinamide adenine dinucleotide ..................0.25g Vitamin B12 .........................................................0.1g Thiamine pyrophosphate ....................................0.1g Guanine·HCl .....................................................0.03g Fe(NO3)3·6H2O.................................................0.02g p-Aminobenzoic acid......................................0.013g Thiamine·HCl ..................................................3.0mg
Preparation of IsoVitaleX: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
Preparation of Medium: Aseptically add 10.0mL of sterile IsoVitaleX enrichment to 990.0L of sterile, cooled GCII agar base. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation and cultivation of fastidious microorganisms, especially Neisseria and Haemophilus species, from a variety of clinical specimens.
Chocolate Tellurite Agar (Tellurite Blood Agar) Composition per liter: Agar ..................................................................10.0g Casein/meat (50/50) peptone ............................10.0g Hemoglobin ......................................................10.0g NaCl....................................................................5.0g K2HPO4...............................................................4.0g Cornstarch...........................................................1.0g KH2PO4...............................................................1.0g K2TeO3 ................................................................0.1g Bio-X enrichment ......................................... 10.0mL
Bio-X Enrichment: Composition per liter: Glucose ...........................................................100.0g L-Cysteine·HCl .................................................25.9g L-Glutamate.......................................................10.0g L-Cystine .............................................................1.1g Adenine...............................................................1.0g
Cholera Medium TCBS
133
Cocarboxylase.....................................................0.1g Guanine·HCl .....................................................0.03g FeNO3 ...............................................................0.02g p-Aminobenzoic acid......................................0.013g Vitamin B12 .......................................................0.01g NAD (nicotinamide adenine dinucleotide) .....250.0mg Thiamine·HCl ..................................................3.0mg pH 7.2 ± 0.2 at 25°C
K2HPO4...............................................................3.5g Cholic acid ..........................................................2.0g (NH4)2SO4 ..........................................................2.0g KH2PO4...............................................................1.5g MgSO4·7H2O ......................................................0.1g CaCl2·2H2O ......................................................0.01g FeSO4·7H2O.....................................................0.5mg pH 7.0 ± 0.2 at 25°C
Preparation of Bio-X Enrichment: Add com-
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.0. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or distribute into sterile tubes.
ponents to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
Caution: Potassium tellurite is toxic. Preparation of Medium: Add components, except Bio-X enrichment, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add filter-sterilized Bio-X enrichment. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the selective isolation and cultivation of Corynebacterium species. Corynebacterium diphtheriae appears as gray-black colonies.
Cholera Medium TCBS Composition per liter: Sucrose..............................................................20.0g Agar ..................................................................14.0g Peptone..............................................................10.0g NaCl ..................................................................10.0g Sodium citrate ...................................................10.0g Na2S2O3·5H2O ..................................................10.0g Ox bile.................................................................8.0g Yeast extract........................................................5.0g Ferric citrate........................................................1.0g Bromthymol Blue .............................................0.04g Thymol Blue .....................................................0.04g pH 8.6 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Do not autoclave. Pour into sterile Petri dishes. Dry agar plates before using.
Use: For the growth of Vibrio cholerae, Vibrio parahaemolyticus, and other Vibrio species.
Cholic Acid Medium Composition per liter: Noble agar.........................................................15.0g
Preparation of Medium: Add components to
Use: For the cultivation and maintenance of Nocardia species and other bacteria that can utilize cholic acid as a carbon source.
Cholera Medium TCBS Composition per liter: Sucrose..............................................................20.0g Agar ..................................................................14.0g Peptone .............................................................10.0g Na2S2O3 ............................................................10.0g Sodium citrate...................................................10.0g NaCl..................................................................10.0g Ox bile ................................................................8.0g Yeast extract........................................................5.0g Ferric citrate........................................................1.0g Bromthymol Blue .............................................0.04g Thymol Blue .....................................................0.04g pH 8.6 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0mL Mix thoroughly. Gently heat while stirring and bring to boiling. Do not autoclave. Cool to 45°C. Pour into sterile Petri dishes.
Use: For the isolation of pathogenic vibrios, especially Vibrio cholerae. This medium is suitable for the growth of Vibrio cholerae, Vibrio parahaemolyticus, and most other Vibrios. Most of the Enterobacteriaceae encountered in faeces are totally suppressed for at least 24 hours. Slight growth of Proteus species and Enterococcus faecalis may occur but the colonies are easily distinguished from vibrio colonies. Whilst inhibiting non-vibrios, it promotes rapid growth of pathogenic vibrios after overnight incubation at 35°C. Vibrio cholerae El Tor biotype forms yellow colonies, Vibrio parahaemolyticus forms blue-green colonies, Vibrio alginolyticus forms yellow colonies, Vibrio metschnikovii forms yellow col-
134
Chopped Meat Agar
onies, Vibrio fluvialis forms yellow colonies, Vibrio vulnificus forms blue-green colonies, Vibrio mimicus forms blue-green colonies, Enterococcus species form yellow colonies, Proteus species form yellowgreen colonies, Pseudomonas species form bluegreen colonies and some strains of Aeromonas hydrophila produce yellow colonies, but Plesimonas shigelloides does not usually grow well on this medium.
Chopped Meat Agar
ue boiling for 15 min without stirring. Cool to room temperature. Remove fat from surface. Filter and retain both meat particles and filtrate. Adjust volume of filtrate to 1.0L with distilled/deionized water. Add pancreatic digest of casein, K2HPO4, yeast extract, and resazurin. Gently heat and bring to boiling. Boil for 1–2 min. Add L-cysteine·HCl. Mix thoroughly. Distribute 7.0mL into tubes that contain meat particles (1 part meat particles to 5 parts fluid). Autoclave for 30 min at 15 psi pressure–121°C.
Use: For the cultivation of various anaerobes.
Composition per liter: Ground meat, fat free ......................................500.0g Pancreatic digest of casein................................30.0g Agar ..................................................................15.0g K2HPO4 ...............................................................5.0g Yeast extract........................................................5.0g L-Cysteine·HCl ...................................................0.5g Resazurin .........................................................1.0mg NaOH (1N solution)...................................... 25.0mL pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Use lean beef or horse meat. Remove fat and connective tissue. Grind finely. Add ground meat and 25.0mL of NaOH solution to distilled/deionized water and bring volume to 1025.0mL. Gently heat and bring to boiling. Continue boiling for 15 min without stirring. Cool to room temperature. Remove fat from surface. Filter and retain both meat particles and filtrate. Adjust volume of filtrate to 1.0L with distilled/deionized water. Add pancreatic digest of casein, agar, K2HPO4, yeast extract, and resazurin. Gently heat and bring to boiling. Boil for 1–2 min. Add L-cysteine·HCl. Mix thoroughly. Distribute 7.0mL into tubes that contain meat particles (1 part meat particles to 5 parts fluid). Autoclave for 30 min at 15 psi pressure–121°C.
Use: For the cultivation of various anaerobes.
Chopped Meat Broth Composition per liter: Ground meat, fat free ......................................500.0g Pancreatic digest of casein................................30.0g K2HPO4 ...............................................................5.0g Yeast extract........................................................5.0g L-Cysteine·HCl ...................................................0.5g Resazurin .........................................................1.0mg NaOH (1N solution)...................................... 25.0mL pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Use lean beef or horse meat. Remove fat and connective tissue. Grind finely. Add ground meat and 25.0mL of NaOH solution to distilled/deionized water and bring volume to 1025.0mL. Gently heat and bring to boiling. Contin-
Chopped Meat Broth with Carbohydrates (DSMZ Medium 110) Composition per liter: Ground meat, fat free......................................500.0g Pancreatic digest of casein................................30.0g K2HPO4...............................................................5.0g Yeast extract........................................................5.0g Glucose ...............................................................4.0g Cellobiose ...........................................................1.0g Maltose ...............................................................1.0g Starch, soluble.....................................................1.0g L-Cysteine·HCl ...................................................0.5g Resazurin .........................................................1.0mg NaOH (1N solution)...................................... 25.0mL pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Use lean beef or horse meat. Remove fat and connective tissue. Grind finely. Add ground meat and 25.0mL of NaOH solution to distilled/deionized water and bring volume to 1025.0mL. Gently heat and bring to boiling. Continue boiling for 15 min. without stirring. Cool to room temperature. Remove fat from surface. Filter and retain both meat particles and filtrate. Adjust volume of filtrate to 1.0L with distilled/deionized water. Add pancreatic digest of casein, K2HPO4, yeast extract, and resazurin. Gently heat and bring to boiling. Boil for 1–2 min. Add glucose, cellobiose, maltose, and soluble starch. Add L-cysteine·HCl. Mix thoroughly. Distribute 7.0mL into tubes that contain meat particles (1 part meat particles to 5 parts fluid). Autoclave for 30 min at 15 psi pressure–121°C.
Use: For the cultivation of numerous anaerobes.
Chopped Meat Broth with Formate and Fumarate (LMG Medium 69) Composition per liter: Ground meat, fat free......................................500.0g Pancreatic digest of casein................................30.0g K2HPO4...............................................................5.0g
Chopped Meat Carbohydrate Medium Yeast extract........................................................5.0g L-Cysteine·HCl ...................................................0.5g Resazurin .........................................................1.0mg NaOH (1N solution)...................................... 25.0mL Formate-fumarate solution.............................. 7.7mL pH 7.0 ± 0.2 at 25°C
Formate-Fumarate Solution: Composition per 100.0mL: Sodium formate...................................................6.0g Fumaric acid .......................................................6.0g
Preparation of Formate-Fumarate Solution: Add components to distilled/deionized water and bring volume to 100.0mL. Adjust pH to 7.0. Filter sterilize.
Preparation of Medium: Use lean beef or horse meat. Remove fat and connective tissue. Grind finely. Add ground meat and 25.0mL of NaOH solution to distilled/deionized water and bring volume to 1025mL. Gently heat and bring to boiling. Continue boiling for 15 min without stirring. Cool to room temperature. Remove fat from surface. Filter and retain both meat particles and filtrate. Adjust volume of filtrate to 1.0L with distilled/deionized water. Add pancreatic digest of casein, agar, K2HPO4, yeast extract, and resazurin. Gently heat and bring to boiling. Boil for 1–2 min. Add L-cysteine·HCl. Mix thoroughly. Distribute 6.5mL into tubes that contain meat particles (1 part meat particles to 5 parts fluid). Autoclave for 30 min at 15 psi pressure–121°C. Cool to 25°C. Aseptically add 50 µL of sterile formate/fumarate solution to each tube prior to inoculation.
Use: For the cultivation of various Clostridium spp.
Chopped Meat Broth with Vitamin K1 (LMG Medium 70) Composition per liter: Ground meat, fat free ......................................500.0g Pancreatic digest of casein................................30.0g K2HPO4 ...............................................................5.0g Yeast extract........................................................5.0g L-Cysteine·HCl ...................................................0.5g Resazurin .........................................................1.0mg NaOH (1N solution)...................................... 25.0mL Vitamin K1 solution ........................................ 7.7mL pH 7.0 ± 0.2 at 25°C
Vitamin K1 Solution: Composition per 50.0mL: Ethanol (20% solution) ................................. 50.0mL Vitamin K1 ....................................................... 0.7gL
Preparation of Vitamin K1 Solution: Mix components. Filter sterilize. Store solution protected from light at 5°C. Discard after one month.
135
Preparation of Medium: Use lean beef or horse meat. Remove fat and connective tissue. Grind finely. Add ground meat and 25.0mL of NaOH solution to distilled/deionized water and bring volume to 1025.0mL. Gently heat and bring to boiling. Continue boiling for 15 min without stirring. Cool to room temperature. Remove fat from surface. Filter and retain both meat particles and filtrate. Adjust volume of filtrate to 1.0L with distilled/deionized water. Add pancreatic digest of casein, agar, K2HPO4, yeast extract, and resazurin. Gently heat and bring to boiling. Boil for 1–2 min. Add L-cysteine·HCl. Mix thoroughly. Distribute 6.5mL into tubes that contain meat particles (1 part meat particles to 5 parts fluid). Autoclave for 30 min at 15 psi pressure–121°C. Cool to 25°C. Aseptically add 50.0µL of sterile vitamin K1 solution to each tube prior to inoculation.
Use: For the cultivation of various Clostridium spp.
Chopped Meat Carbohydrate Medium Composition per 1240.0mL: Peptone .............................................................30.0g K2HPO4...............................................................5.0g Yeast extract........................................................5.0g Cellobiose ...........................................................1.0g Maltose ...............................................................1.0g Starch ..................................................................1.0g L-Cysteine·HCl·H2O............................................0.5g Chopped meat extract filtrate............................. 1.0L Chopped meat extract solids....................... 200.0mL Resazurin (0.025% solution) .......................... 4.0mL pH 7.0 ± 0.2 at 25°C
Chopped Meat Extract: Composition per liter: Beef or horse meat ..........................................500.0g NaOH (1N solution)...................................... 25.0mL
Preparation of Chopped Meat Extract: Use lean beef or horse meat. Remove fat and connective tissue. Grind. Add meat and NaOH to distilled/deionized water and bring volume to 1.0L. Gently heat and bring to boiling while stirring. Cool to 25°C. Remove fat from surface. Filter. Reserve ground meat particles and filtrate. Add distilled/deionized water to filtrate and bring volume to 1.0L. Preparation of Medium: To 1.0L of chopped meat extract filtrate, add the remaining components, except the L-cysteine·HCl·H2O and chopped meat solids. Mix thoroughly. Gently heat to boiling. Cool to room temperature. Add the L-cysteine·HCl·H2O. Adjust pH to 7.0. Distribute 1 part chopped meat solids (by volume) and 5 parts of liquid (by volume) into tubes under O2-free 97% N2 + 3% H2. Cap with rub-
136
Chopped Meat Glucose Agar
ber stoppers and place tubes in a press. Autoclave for 15 min at 15 psi pressure–121°C with fast exhaust.
Use: For the cultivation of anaerobic bacteria, including Clostridium species, Eubacterium species, and Gemmiger formicilis.
Chopped Meat Glucose Agar (LMG Medium 68) Composition per liter: Ground meat, fat free ......................................500.0g Pancreatic digest of casein................................30.0g Agar ..................................................................15.0g Glucose .............................................................10.0g K2HPO4 ...............................................................5.0g Yeast extract........................................................5.0g L-Cysteine·HCl ...................................................0.5g Resazurin .........................................................1.0mg NaOH (1N solution)...................................... 25.0mL pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Use lean beef or horse meat. Remove fat and connective tissue. Grind finely. Add ground meat and 25.0mL of NaOH solution to distilled/deionized water and bring volume to 1025.0mL. Gently heat and bring to boiling. Continue boiling for 15 min without stirring. Cool to room temperature. Remove fat from surface. Filter and retain both meat particles and filtrate. Adjust volume of filtrate to 1.0L with distilled/deionized water. Add pancreatic digest of casein, agar, K2HPO4, yeast extract, and resazurin. Gently heat and bring to boiling. Boil for 1–2 min. Add L-cysteine·HCl. Mix thoroughly. Distribute 7.0mL into tubes that contain meat particles (1 part meat particles to 5 parts fluid). Autoclave for 30 min at 15 psi pressure–121°C.
Use: For the cultivation of various Clostridium spp.
Chopped Meat Glucose Broth (LMG Medium 68) Composition per liter: Ground meat, fat free ......................................500.0g Pancreatic digest of casein................................30.0g Glucose .............................................................10.0g K2HPO4 ...............................................................5.0g Yeast extract........................................................5.0g L-Cysteine·HCl ...................................................0.5g Resazurin .........................................................1.0mg NaOH (1N solution)...................................... 25.0mL pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Use lean beef or horse meat. Remove fat and connective tissue. Grind finely. Add ground meat and 25.0mL of NaOH solution to distilled/deionized water and bring volume to 1025.0mL. Gently heat and bring to boiling. Contin-
ue boiling for 15 min without stirring. Cool to room temperature. Remove fat from surface. Filter and retain both meat particles and filtrate. Adjust volume of filtrate to 1.0L with distilled/deionized water. Add pancreatic digest of casein, agar, K2HPO4, yeast extract, and resazurin. Gently heat and bring to boiling. Boil for 1–2 min. Add L-cysteine·HCl. Mix thoroughly. Distribute 7.0mL into tubes that contain meat particles (1 part meat particles to 5 parts fluid). Autoclave for 30 min at 15 psi pressure–121°C.
Use: For the cultivation of various Clostridium spp.
Chopped Meat Glucose Medium Composition per 1240.0mL: Peptone .............................................................30.0g K2HPO4...............................................................5.0g Yeast extract........................................................5.0g Glucose ...............................................................5.0g L-Cysteine·HCl·H2O............................................0.5g Chopped meat extract filtrate............................. 1.0L Chopped meat extract solids....................... 200.0mL Resazurin (0.025% solution) .......................... 4.0mL pH 7.0 ± 0.2 at 25°C
Chopped Meat Extract: Composition per liter: Beef or horse meat ..........................................500.0g NaOH (1N solution)...................................... 25.0mL
Preparation of Chopped Meat Extract: Use lean beef or horse meat. Remove fat and connective tissue. Grind. Add meat and NaOH to distilled/deionized water and bring volume to 1.0L. Gently heat and bring to boiling while stirring. Cool to 25°C. Remove fat from surface. Filter. Reserve ground meat particles and filtrate. Add distilled/deionized water to filtrate and bring volume to 1.0L. Preparation of Medium: To 1.0L of chopped meat extract filtrate, add the remaining components, except L-cysteine·HCl·H2O and chopped meat solids. Mix thoroughly. Gently heat to boiling. Cool to room temperature. Add the L-cysteine·HCl·H2O. Adjust pH to 7.0. Distribute 1 part chopped meat solids (by volume) and 5 parts of liquid (by volume) into tubes under O2-free 97% N2 + 3% H2. Cap with rubber stoppers and place tubes in a press. Autoclave for 15 min at 15 psi pressure–121°C with fast exhaust. Use: For the cultivation of Clostridium species and Selenomonas noxia.
Chopped Meat Medium Composition per 1205.0mL: Peptone .............................................................30.0g K2HPO4...............................................................5.0g Yeast extract........................................................5.0g
Chopped Meat Medium, Modified
137
L-Cysteine·HCl·H2O............................................0.5g
Chopped meat extract filtrate............................. 1.0L Chopped meat extract solids ....................... 200.0mL Resazurin (0.025% solution)........................... 4.0mL pH 7.0 ± 0.2 at 25°C
ized water and bring volume to 1.0L. Gently heat and bring to boiling while stirring. Cool to 25°C. Remove fat from surface. Filter. Reserve ground meat particles and filtrate. Add distilled/deionized water to filtrate and bring volume to 1.0L.
Chopped Meat Extract: Composition per liter:
Formate-Fumarate Solution: Composition per 100.0mL:
Beef or horse meat ..........................................500.0g NaOH (1N solution)...................................... 25.0mL
Sodium formate ..................................................6.0g Fumaric acid .......................................................6.0g
Preparation of Chopped Meat Extract: Use lean beef or horse meat. Remove fat and connective tissue. Grind. Add meat and NaOH to distilled/deionized water and bring volume to 1.0L. Gently heat and bring to boiling while stirring. Cool to 25°C. Remove fat from surface. Filter. Reserve ground meat particles and filtrate. Add distilled/deionized water to filtrate and bring volume to 1.0L.
Preparation of Formate-Fumarate Solution:
Preparation of Medium: To 1.0L of chopped meat extract filtrate, add the remaining components, except the L-cysteine·HCl·H2O and chopped meat solids. Mix thoroughly. Gently heat to boiling. Cool to room temperature. Add the L-cysteine·HCl·H2O. Adjust pH to 7.0. Distribute 1 part chopped meat solids (by volume) and 5 parts of liquid (by volume) into tubes under O2-free 97% N2 + 3% H2. Cap with rubber stoppers and place tubes in a press. Autoclave for 15 min at 15 psi pressure–121°C with fast exhaust. Use: For the cultivation and maintenance of a variety of anaerobic bacteria, including Bacteroides species, Bifidobacterium species, Capnocytophaga species, Clostridium species, Eubacterium species, Fusobacterium species, and others.
Chopped Meat Medium with Formate and Fumarate Composition per 1230.0mL: Peptone..............................................................30.0g K2HPO4 ...............................................................5.0g Yeast extract........................................................5.0g L-Cysteine·HCl·H2O............................................0.5g Chopped meat extract filtrate............................. 1.0L Chopped meat extract solids ....................... 200.0mL Resazurin (0.025% solution)........................... 4.0mL Formate-fumarate solution............................ 0.05mL pH 7.0 ± 0.2 at 25°C
Chopped Meat Extract: Composition per liter: Beef or horse meat ..........................................500.0g NaOH (1N solution)...................................... 25.0mL
Preparation of Chopped Meat Extract: Use lean beef or horse meat. Remove fat and connective tissue. Grind. Add meat and NaOH to distilled/deion-
Add components to distilled/deionized water and bring volume to 100.0mL. Adjust pH to 7.0. Filter sterilize.
Preparation of Medium: To 1.0L of chopped meat extract filtrate, add the remaining components, except the L-cysteine·HCl·H2O, formate-fumarate solution, and chopped meat solids. Mix thoroughly. Gently heat to boiling. Cool to room temperature. Add the L-cysteine·HCl·H2O. Adjust pH to 7.0. Distribute 1 part chopped meat solids (by volume) and 5 parts of liquid (by volume) into tubes under O2-free 97% N2 + 3% H2. Cap with rubber stoppers and place tubes in a press. Autoclave for 15 min at 15 psi pressure–121°C with fast exhaust. Prior to inoculation, add 0.05mL of formate-fumarate solution to each tube containing approximately 6.5mL of chopped meat medium.
Use: For the cultivation and maintenance of Bacteroides ureolyticus and Wolinella species.
Chopped Meat Medium, Modified Composition per 1230.0mL: Pancreatic digest of casein................................30.0g Peptone .............................................................30.0g Agar ..................................................................20.0g K2HPO4...............................................................5.0g Yeast extract........................................................5.0g L-Cysteine·HCl·H2O............................................0.5g Chopped meat extract filtrate............................. 1.0L Chopped meat extract solids....................... 200.0mL Hemin solution.............................................. 10.0mL Resazurin (0.025% solution) .......................... 4.0mL Vitamin K1 solution ........................................ 0.2mL pH 7.0 ± 0.2 at 25°C
Chopped Meat Extract: Composition per liter: Beef or horse meat ..........................................500.0g NaOH (1N solution)...................................... 25.0mL
Preparation of Chopped Meat Extract: Use lean beef or horse meat. Remove fat and connective tissue. Grind. Add meat and NaOH to distilled/deionized water and bring volume to 1.0L. Gently heat and bring to boiling while stirring. Cool to 25°C. Remove fat from surface. Filter. Reserve ground meat parti-
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Chopped Meat Medium, Modified with Formate and Fumarate
cles and filtrate. Add distilled/deionized water to filtrate and bring volume to 1.0L.
Chopped Meat Extract: Composition per liter:
Hemin Solution: Composition per 100.0mL:
Beef or horse meat ..........................................500.0g NaOH (1N solution)...................................... 25.0mL
Vitamin K1 Solution: Composition per 30.0mL:
Preparation of Chopped Meat Extract: Use lean beef or horse meat. Remove fat and connective tissue. Grind. Add meat and NaOH to distilled/deionized water and bring volume to 1.0L. Gently heat and bring to boiling while stirring. Cool to 25°C. Remove fat from surface. Filter. Reserve ground meat particles and filtrate. Add distilled/deionized water to filtrate and bring volume to 1.0L.
Ethanol (95% solution) ................................. 30.0mL Vitamin K1 .................................................... 0.15mL
Hemin Solution: Composition per 100.0mL:
Hemin................................................................0.05g NaOH (1N solution)........................................ 1.0mL
Preparation of Hemin Solution: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly.
Preparation of Vitamin K1 Solution: Mix components. Store solution protected from light at 5°C. Discard after 1 month.
Preparation of Medium: To 1.0L of chopped meat extract filtrate, add the remaining components, except the L-cysteine·HCl·H2O, hemin solution, vitamin K1 solution, and chopped meat solids. Mix thoroughly. Gently heat to boiling. Cool to room temperature. Add the L-cysteine·HCl·H2O, hemin solution, and vitamin K1 solution. Adjust pH to 7.0. Distribute 1 part chopped meat solids (by volume) and 5 parts of liquid (by volume) into tubes under O2free 97% N2 + 3% H2. Cap with rubber stoppers and place tubes in a press. Autoclave for 15 min at 15 psi pressure–121°C with fast exhaust.
Use: For the cultivation and maintenance of a variety of anaerobic bacteria, including Actinomyces species, Bacteroides species, Clostridium species, Eubacterium species, Fusobacterium species, Peptostreptococcus species, Porphyromonas species, Prevotella species, Propionibacterium species, Selenomonas species, and others.
Chopped Meat Medium, Modified with Formate and Fumarate Composition per 1230.0mL: Pancreatic digest of casein................................30.0g Peptone..............................................................30.0g Agar ..................................................................20.0g K2HPO4 ...............................................................5.0g Yeast extract........................................................5.0g L-Cysteine·HCl·H2O............................................0.5g Chopped meat extract filtrate............................. 1.0L Chopped meat extract solids ....................... 200.0mL Hemin solution.............................................. 10.0mL Resazurin (0.025% solution)........................... 4.0mL Formate-fumarate solution............................ 0.25mL Vitamin K1 solution ........................................ 0.2mL pH 7.0 ± 0.2 at 25°C
Hemin ...............................................................0.05g NaOH (1N solution)........................................ 1.0mL
Preparation of Hemin Solution: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly.
Formate-Fumarate Solution: Composition per 100.0mL: Sodium formate ..................................................6.0g Fumaric acid .......................................................6.0g
Preparation of Formate-Fumarate Solution: Add components to distilled/deionized water and bring volume to 100.0mL. Adjust pH to 7.0. Filter sterilize.
Vitamin K1 Solution: Composition per 30.0mL: Ethanol (95% solution) ................................. 30.0mL Vitamin K1 .................................................... 0.15mL
Preparation of Vitamin K1 Solution: Mix com-
ponents. Store solution protected from light at 5°C. Discard after one month.
Preparation of Medium: To 1.0L of chopped meat extract filtrate, add the remaining components, except the L-cysteine·HCl·H2O, hemin solution, vitamin K1 solution, formate-fumarate solution, and chopped meat solids. Mix thoroughly. Gently heat to boiling. Cool to room temperature. Add the L-cysteine·HCl·H2O, hemin solution, and vitamin K1 solution. Adjust pH to 7.0. Distribute 1 part chopped meat solids (by volume) and 5 parts of liquid (by volume) into tubes under O2-free 97% N2 + 3% H2. Cap with rubber stoppers and place tubes in a press. Autoclave for 15 min at 15 psi pressure–121°C with fast exhaust. Prior to inoculation, add 0.25mL of formatefumarate solution to each tube containing approximately 5.0mL of chopped meat medium, modified. Use: For the cultivation and maintenance of Bacteroides gracilis, Bacteroides ureolyticus, Campylobacter mucosalis, and Wolinella succinogenes.
Christensen Citrate Sulfide Medium
Christensen Agar Composition per liter: Agar ..................................................................15.0g NaCl ....................................................................5.0g Sodium citrate .....................................................3.0g KH2PO4 ...............................................................1.0g L-Cysteine·HCl·H2O ...........................................0.1g Phenol Red.....................................................12.0mg pH 6.9 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Dispense into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes. Allow tubes to cool in a slanted position.
Use: For the differentiation of enteric pathogens, especially members of the Enterobacteriaceae, and coliforms based on their ability to utilize citrate as a carbon source. Bacteria that can utilize citrate turn the medium pink-red.
139
Yeast extract........................................................0.5g Ferric ammonium citrate.....................................0.4g L-Cysteine·HCl·H2O ...........................................0.1g Na2S2O5 ............................................................0.08g Phenol Red.....................................................12.0mg pH 6.9 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Dispense into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes. Allow tubes to cool in a slanted position.
Use: For the differentiation of enteric pathogens, especially members of the Enterobacteriaceae, and coliforms based on their ability to utilize citrate as a carbon source. Bacteria that can utilize citrate turn the medium pink-red.
Christensen Citrate Agar, Modified (Citrate Agar) Composition per liter:
Christensen Agar Composition per liter: Agar ..................................................................15.0g NaCl ....................................................................5.0g Sodium citrate .....................................................3.0g KH2PO4 ...............................................................1.0g Yeast extract........................................................0.5g Glucose ...............................................................0.2g L-Cysteine·HCl·H2O ...........................................0.1g Phenol Red.....................................................12.0mg pH 6.9 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Dispense into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes. Allow tubes to cool in a slanted position.
Use: For the differentiation of enteric pathogens, especially members of the Enterobacteriaceae, and coliforms based on their ability to utilize citrate as a carbon source. Bacteria that can utilize citrate turn the medium pink-red.
Christensen Citrate Agar Composition per liter: Agar ..................................................................15.0g NaCl ....................................................................5.0g Sodium citrate .....................................................3.0g KH2PO4 ...............................................................1.0g
Agar ..................................................................12.0g NaCl....................................................................5.0g Sodium citrate.....................................................3.8g KH2PO4...............................................................1.0g Yeast extract........................................................0.5g Glucose ...............................................................0.2g L-Cysteine·HCl·H2O ...........................................0.1g Phenol Red........................................................0.02g pH 6.7 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Dispense into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes. Allow tubes to cool in a slanted position.
Use: For the differentiation of enteric pathogens, especially members of the Enterobacteriaceae, and coliforms based on their ability to utilize citrate as a carbon source. Bacteria that can utilize citrate turn the medium pink-red.
Christensen Citrate Sulfide Medium Composition per liter: Agar ..................................................................15.0g NaCl....................................................................5.0g Sodium citrate·2H2O...........................................3.0g KH2HPO4 ............................................................1.0g Yeast extract........................................................0.5g Ferric citrate........................................................0.2g Ammonium citrate ..............................................0.2g Glucose ...............................................................0.2g L-Cysteine·HCl·H2O ...........................................0.1g
140
Christensen’s Urea Agar
Na2S2O3·5H2O ..................................................0.08g Phenol Red......................................................0.012g pH 6.7± 0.2 at 25°C
Source: CHROMagar Candida is available from
Preparation of Medium: Add components to dis-
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat in a boiling water bath or steam bath. Shake periodically during heating to dissolve components. Heat long enough with shaking every 5 min to ensure complete dissolution. Do not overheat. Cool to 45–50°C. Pour into sterile Petri dishes.
tilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Dispense into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes. Allow tubes to cool in a slanted position.
Use: For the differentiation of enteric pathogens, especially members of the Enterobacteriaceae, and coliforms based on their ability to utilize citrate as a carbon source and production of H2S. Bacteria that can utilize citrate turn the medium pink-red. H2S production appears as a blackening of the butt of the tube.
CHROMagar Microbiology.
Preparation of Medium: Add components to
Use: For the differentiation of Candida spp. Specific Candida spp. give characteristic color reactions, e.g., Candida albicans produce distinctive green colonies and Candida tropicalis produce distinctive dark bluegray colonies.
Christensen’s Urea Agar
CHROMagar E. coli
Composition per liter: Agar ..................................................................15.0g NaCl ....................................................................5.0g KH2PO4 ...............................................................2.0g Peptone................................................................1.0g Glucose ...............................................................1.0g Phenol Red......................................................0.012g Urea solution............................................... 100.0mL pH 6.8 ± 0.1 at 25°C
Urea Solution: Composition per 100.0mL: Urea...................................................................20.0g
Preparation of Urea: Add urea to 100.0mL of distilled/deionized water. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except urea solution, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50–55°C. Aseptically add 100.0mL of sterile urea solution. Mix thoroughly. Pour into Petri dishes or distribute into sterile tubes. Allow tubes to solidify in a slanted position.
Use: For the differentiation of a variety of microorganisms, especially members of the Enterobacteriaceae, aerobic actinomycetes, streptococci, and nonfermenting Gram-negative bacteria, on the basis of urease production.
CHROMagar Candida Composition per liter: Glucose .............................................................20.0g Agar ..................................................................15.0g Peptone..............................................................10.0g Chromogenic mix ...............................................2.0g Chloramphenicol.................................................0.5g
Composition per liter: Proprietary
Source: CHROMagar E. coli is available from CHROMagar Microbiology. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat in a boiling water bath or steam bath. Shake periodically during heating to dissolve components. Heat long enough with shaking every 5 min to ensure complete dissolution. Do not overheat. Adding tellurite can increase specificity. Cool to 45–50°C. Pour into sterile Petri dishes.
Use: For the differentiation and presumptive identification of Eshcrichia coli which forms blue colonies.
CHROMagar ECC Composition per liter: Proprietary
Source: CHROMagar EEC is available from CHROMagar Microbiology. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat in a boiling water bath or steam bath. Shake periodically during heating to dissolve components. Heat long enough with shaking every 5 min to ensure complete dissolution. Do not overheat. Adding tellurite can increase specificity. Cool to 45–50°C. Pour into sterile Petri dishes.
Use: For the differentiation and presumptive identification of Eshcrichia coli and other coliform bacteria which form red colonies.
CHROMagar Vibrio
CHROMagar Listeria Composition per liter: Proprietary
Source: CHROMagar Listeria is available from CHROMagar Microbiology.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat in a boiling water bath or steam bath. Shake periodically during heating to dissolve components. Heat long enough with shaking every 5 min to ensure complete dissolution. Do not overheat. Adding tellurite can increase specificity. Cool to 45–50°C. Pour into sterile Petri dishes.
Use: For the differentiation and presumptive identification of Listeria monocytogenes which form blue colonies surrounded by white halos.
CHROMagar O157 Composition per liter: Proprietary
Source: CHROMagar O157 is available from CHROMagar Microbiology.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat in a boiling water bath or steam bath. Shake periodically during heating to dissolve components. Heat long enough with shaking every 5 min to ensure complete dissolution. Do not overheat. Adding tellurite can increase specificity. Cool to 45–50°C. Pour into sterile Petri dishes.
Use: For the differentiation and presumptive identification of Eshcrichia coli O157.
CHROMagar Orientation Composition per liter:
141
Use: For the differentiation and presumptive identification of Gram-negative bacteria and Enterococcus spp. For use in identifying urinary tract pathogens. Isolates produce characteristic diagnostic colors, e.g., Escherichia coli produces pinto red colonies.
CHROMagar Salmonella Composition per liter: Proprietary
Source: CHROMagar Salmonella is available from CHROMagar Microbiology. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat in a boiling water bath or steam bath. Shake periodically during heating to dissolve components. Heat long enough with shaking every 5 min to ensure complete dissolution. Do not overheat. Cool to 50°C. Pour into sterile Petri dishes.
Use: For the differentiation and presumptive identification of Salmonella spp.
CHROMagar Staph. aureus Composition per liter: Proprietary
Source: CHROMagar Staph. aureus is available from CHROMagar Microbiology.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat in a boiling water bath or steam bath. Shake periodically during heating to dissolve components. Heat long enough with shaking every 5 min to ensure complete dissolution. Do not overheat. Adding an antibiotic such as tobramycin or methicillin can be used to identify resistant strains. Cool to 45–50°C. Pour into sterile Petri dishes.
Peptone..............................................................16.0g Meat extract ......................................................16.0g Peptone..............................................................16.0g Yeast extract......................................................16.0g Agar ..................................................................15.0g Chromogenic mix ...............................................2.0g pH 7.0 ± 0.2 at 25°C
Use: For the differentiation and presumptive identifi-
Source: CHROMagar Orientation is available from
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat in a boiling water bath or steam bath. Shake periodically during heating to dissolve components. Heat long enough with shaking every 5 min to ensure complete dissolution. Do not overheat. Adding tellurite can increase specificity. Cool to 45–50°C. Pour into sterile Petri dishes.
CHROMagar Microbiology.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat in a boiling water bath or steam bath. Shake periodically during heating to dissolve components. Heat long enough with shaking every 5 min to ensure complete dissolution. Do not overheat. Cool to 50°C. Pour into sterile Petri dishes.
cation of Staphylococcus aureus.
CHROMagar Vibrio Composition per liter: Proprietary
Preparation of Medium: Add components to
Source: CHROMagar Vibrio is available from CHROMagar Microbiology.
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Chromogenic Candida Agar
Use: For the differentiation and presumptive identifi-
Source: This medium is available as a premixed
cation of Vibrio parahaemolyiticus which form mauve colonies; Vibrio cholerae form turquoise blue colonies and Vibrio alginolyitcus colonies are colorless.
powder from Oxoid Unipath.
Chromogenic Candida Agar
Differential Lecithin Solution: Composition per 40.0mL: Lecithin ....................................................Proprietary
Composition per liter:
Preparation of Differential Lecithin Solution:
Chromogenic mix .............................................13.6g Agar ..................................................................13.6g Peptone................................................................4.0g Selective supplement solution ...................... 10.0mL pH 6.0 ± 0.2 at 25°C
Selective Supplement Solution: Composition per 20.0mL:
Source: This medium is available as a premixed powder from Oxoid Unipath. Selective Supplement Solution: Composition per 10.0mL: Chloramphenicol..........................................500.0mg
Preparation of Selective Supplement Solution: Add chloramphenicol to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0mL Mix thoroughly. Gently heat while stirring and bring to boiling. Do not autoclave. Cool to 45°C. Pour into sterile Petri dishes.
Use: For the rapid isolation and identification of clinically important Candida species. The medium incorporates two chromogens that indicate the presence of the target enzymes: X-NAG (5-bromo-4chloro-3-indolyl N acetyl ß-D-glucosaminide) detects the activity of hexosaminidase. BCIP (5-bromo6-chloro-3-indolyl phosphate p-toluidine salt) detects alkaline phosphatase activity. An opaque agent has been incorporated into the formulation to improve the color definition on the agar. The broadspectrum antibacterial agent chloramphenicol is added to the agar to inhibit bacterial growth on the plates.
Available as premixed solution.
Nalidixic acid.................................................26.0mg Polymyxin B ..................................................10.0mg Ceftazidime......................................................6.0mg Amphotericin .................................................10.0mg
Preparation of Selective Supplement Solution: Add components to distilled/deionized water and bring volume to 20.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except differential lecithin solution and selective supplement solution, to distilled/deionized water and bring volume to 940.0mL. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 46°C. Aseptially add differential lecithin solution and selective supplement solution. Mix thouroughly. Pour into sterile Petri dishes.
Use: For the isolation, enumeration and presumptive identification of Listeria spp. and Listeria monocytogenes. This selective medium contains the substrate lecithin, which permits differentiation of L. monocytogenes and L. Ivanovii from other Listeria species. Differential activity for all Listeria species is due to the addition of a chromogenic substrate.
Chromogenic MRSA Agar Composition per liter: Proprietary
Chromogenic Listeria Agar
Source: This medium is available as a premixed
Composition per liter:
powder from Oxoid Unipath.
Peptone..............................................................18.5g LiCl ...................................................................15.0g Agar ..................................................................14.0g NaCl ....................................................................9.5g Yeast extract........................................................4.0g Maltose ...............................................................4.0g Sodium pyruvate ................................................2.0g X-glucoside chromogenic mix ...........................0.2g Differential lecithin solution ......................... 40.0mL Selective supplement solution ...................... 20.0mL pH 7.2 ± 0.2 at 25°C
Use: For the detection of methicillin resistant Staphylococcus aureus. The chromogen in this medium detects phosphatase activity, which is present in MRSA strains, producing distinct, easily visible, denim-blue colonies. Antimicrobial compounds within the medium, including cefoxitin, inhibit the growth of competitor organisms to allow accurate diagnosis of MRSA. The medium may be inoculated directly from swabs, or from isolates or culture suspensions. The plate can then be examined for MRSA colonies after a short, 18-hour incubation.
Chromogenic Urinary Tract Infection (UTI) Medium
Chromogenic Salmonella Esterase Agar (CSE Agar) Composition per liter: Agar ..................................................................12.0g Lactose ..............................................................14.6g Peptone................................................................4.0g Tryptone ..............................................................4.0g Tween 20.............................................................3.0g Lab Lemco ..........................................................3.0g Na3-citrate dihydrate ...........................................0.5g L-cysteine ........................................................0.128g Tris ....................................................................0.06g SLA-octonoate solution ................................ 50.0mL Novobiocin solution...................................... 10.0mL Ethyl 4-dimethylaminobenzoate solution ..... 10.0mL pH 7.0 ± 0.2 at 25°C
Novobiocin Solution: Composition per 10.0mL: Novobiocin.....................................................70.0mg
Preparation of Novobiocin Solution: Add novobiocin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Ethyl 4-dimethylaminobenzoate Solution: Composition per 10.0mL: Ethyl 4-dimethylaminobenzoate .......................0.35g Methanol ......................................................... 8.0mL
Preparation of Ethyl 4-dimethylaminobenzoate Solution: Add ethyl 4-dimethylaminobenzoate to 8.0mL methanol. Mix thoroughly. Bring volume to 10.0mL with distilled/deionized water. Mix thoroughly. Filter sterilize.
SLA-Octonoate Solution: Composition per 50.0mL: 4-[2-(4-octanoyloxy-3,5-dimethoxyphenyl)vinyl]-quinolinium-1-(propan-3-yl carboxylic acid) bromide (SLPA-octanoate; bromide form) ...........0.3223g
Preparation of SLA-Octonoate Solution: Add SLA-octonoate to distilled/deionized water and bring volume to 50.0mL. Mix thoroughly. Filter sterilize. Preparation of Medium: Add components, except novobiocin solution, SLA-octonoate solution, and ethyl 4-dimethylaminobenzoate solution, to distilled/deionized water and bring volume to 920.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C. Aseptically add 10.0mL novobiocin solution, 50.0mL SLA-octonoate solution, and 10.0mL ethyl 4-dimethylaminobenzoate solution. Mix thoroughly. Pour into sterile Petri dishes.
Use: For the detection of Salmonella spp. in clinical specimens. For the differentiation of Salmonella spp.
143
Chromogenic Substrate Broth Composition per liter: NaCl..................................................................10.0g HEPES (N-[2-Hydroxyethyl] piperazine-N´-[2-ethanesulfonic acid]) buffer ....................................6.9g (NH4)2SO4 ..........................................................5.0g o-Nitrophenyl-β-D-galactopyranoside ................0.5g Solanium .............................................................0.5g MgSO4 ................................................................0.1g 4-Methylumbelliferyl-β-D-glucuronide ..........0.075g CaCl2 .................................................................0.05g Na2SO3 ..............................................................0.04g Amphotericin B ...............................................1.0mg MnSO4 .............................................................0.5mg ZnSO4 ..............................................................0.5mg
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the detection of coliform bacteria based on their hydrolysis of chromogenic substrates by production of β-D-galactopyranosidase. Bacteria that produce β-D-galactopyranosidase turn the medium yellow.
Chromogenic Urinary Tract Infection (UTI) Medium Composition per liter: Chromogenic mix .............................................26.3g Peptone .............................................................15.0g Agar ..................................................................15.0g pH 6.8 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 50°C. Pour into sterile Petri dishes.
Use: For the presumptive identification and differentiation of all the main microorganisms that cause urinary tract infections (UTIs). The medium contains two specific chromogenic substrates which are cleaved by enzymes produced by Enterococcus spp., Escherichia coli, and coliforms. In addition, it contains phenylalanine and tryptophan which provide an indication of tryptophan deaminase activity, indicating the presence of Proteus spp., Morganella spp., and Providencia spp. It is based on electrolyte deficient CLED Medium which provides a valuable noninhibitory diagnostic agar for plate culture of other urinary organisms, whilst preventing the swarming of Proteus spp. One chromogen, X-Gluc, is targeted
144
Chromogenic UTI Medium, Clear
towards β-glucosidase, and allows the specific detection of enterococci through the formation of blue colonies. The other chromogen, Red-Gal, is cleaved by the enzyme β-galactosidase which is produced by Escherichia coli, resulting in pink colonies. Cleavage of both chromogens occurs in the presence of coliforms, resulting in purple colonies. The medium also contains tryptophan which acts as an indicator of tryptophan deaminase activity, resulting in colonies of Proteus, Morganella, and Providencia spp. appearing brown.
Chromogenic UTI Medium, Clear Composition per liter: Peptone..............................................................15.0g Agar ..................................................................15.0g Chromogenic mix .............................................13.0g pH 7.0 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 50°C. Pour into sterile Petri dishes.
Use: For the presumptive identification and differentiation of all the main microorganisms that cause urinary tract infections (UTIs). This medium uses the same chromogenic substrates as the existing opaque Chromogenc UTI Medium but has a clear background to make multiple sample testing easier. The medium contains two specific chromogenic substrates which are cleaved by enzymes produced by Enterococcus spp., E. coli, and coliforms. In addition, it contains tryptophan which indicates tryptophan deaminase activity (TDA), indicating the presence of Proteus spp. It is based on Cystine Lactose Electrolyte Deficient (CLED) Medium which provides a valuable non-inhibitory diagnostic agar for plate culture of other urinary organisms, whilst preventing the swarming of Proteus spp. The chromogen, X-glucoside, is targeted towards ß-glucosidase enzyme activity, and allows the specific detection of enterococci through the formation of blue colonies. The other chromogen, Red-Galactoside, is cleaved by the enzyme ß-galactosidase which is produced by E. coli, resulting in pink colonies. Cleavage of both the chromogens by members of the coliform group, results in purple colonies. The medium also contains tryptophan which acts as an indicator of tryptophan deaminase activity (TDA), resulting in halos around the colonies of Proteus, Morganella, and Providencia spp.
CIN Agar (Yersinia Selective Agar) (Cefsulodin Irgasan Novobiocin Agar) Composition per liter: Mannitol............................................................20.0g Agar ..................................................................12.0g Pancreatic digest of gelatin...............................10.0g Beef extract.........................................................5.0g Peptic digest of animal tissue .............................5.0g Sodium pyruvate.................................................2.0g Yeast extract........................................................2.0g NaCl....................................................................1.0g Sodium deoxycholate..........................................0.5g Neutral Red.......................................................0.03g Cefsulodin.......................................................0.015g Irgasan (triclosan) ............................................4.0mg Novobiocin ......................................................2.5mg Crystal Violet ...................................................1.0mg pH 7.4 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components, except cefsulodin and novobiocin, to distilled/deionized water and bring volume to 1.0L. Heat, mixing continuously, until boiling. Do not autoclave. Cool to 45°–50°C. Aseptically add cefsulodin and novobiocin. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the selective isolation and differentiation of Yersinia enterocolitica from a variety of clinical and nonclinical specimens based on mannitol fermentation. Yersinia enterocolitica appears as “bull’s eye” colonies with deep red centers surrounded by a transparent periphery.
Citrate Medium, Koser’s Modified Composition per liter: NaCl....................................................................5.0g Citric acid............................................................2.0g (NH4)H2PO4........................................................1.0g K2HPO4 ..............................................................1.0g MgSO4·7H2O ......................................................0.2g pH 6.8 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 6.8. Distribute into tubes in 5.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation and differentiation of bacteria based on their ability to utilize citrate as a carbon source.
Clostridium botulinum Isolation Agar
CLED Agar (Cystine Lactose Electrolyte Deficient Agar) (Brolacin Agar) Composition per liter: Agar ..................................................................15.0g Lactose ..............................................................10.0g Pancreatic digest of casein..................................4.0g Pancreatic digest of gelatin .................................4.0g Beef extract .........................................................3.0g L-Cystine .........................................................0.128g Bromthymol Blue .............................................0.02g pH 7.3 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 50°–55°C. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation, enumeration, and presumptive identification of microorganisms from urine.
CLED Agar with Andrade Indicator (Cystine Lactose Electrolyte Deficient Agar with Andrade Indicator) Composition per liter: Agar ..................................................................15.0g Pancreatic digest of casein................................10.0g Peptone................................................................4.0g Beef extract .........................................................3.0g L-Cystine .........................................................0.128g Bromthymol Blue .............................................0.02g Andrade indicator ......................................... 10.0mL pH 7.5 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath.
Caution: Acid Fuchsin is a potential carcinogen and care must be taken to avoid inhalation of the powdered dye and contamination of the skin.
Andrade’s Indicator: Composition per 100.0mL: NaOH (1N solution)...................................... 16.0mL Acid Fuchsin .......................................................0.1g
Preparation of Andrade’s Indicator: Add Acid Fuchsin to NaOH solution and bring volume to 100.0mL with distilled/deionized water.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure–
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121°C. Cool to 50°–55°C. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the differentiation of microorganisms based on colony characteristics.
Clostridia Medium Composition per liter: Sodium L-lactate ...............................................10.0g Sodium acetate....................................................8.0g K2HPO4...............................................................0.5g (NH4)2·7H2O.......................................................0.5g Sodium thioglycolate ..........................................0.5g Yeast extract........................................................0.5g MgSO4·7H2O ......................................................0.1g FeSO4·7H2O......................................................0.02g p-Aminobenzoate..........................................100.0µg Biotin ................................................................0.1µg pH 6.0–7.0 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 6.0–7.0. Distribute into tubes or flasks. Autoclave for 20 min at 15 psi pressure–121°C.
Use: For the isolation and cultivation of Clostridium species that ferment lactate and acetate.
Clostridium botulinum Isolation Agar (CBI Agar) Composition per 1033.0mL: Egg yolk agar base...................................... 900.0mL Egg yolk emulsion, 50%............................. 100.0mL Cycloserine solution ..................................... 25.0mL Sulfamethoxazole solution.............................. 4.0mL Trimethoprim solution .................................... 4.0mL pH7.4 ± 0.2 at 25°C
Egg Yolk Agar Base: Composition per 900.0mL: Pancreatic digest of casein................................40.0g Agar ..................................................................20.0g Na2HPO4 .............................................................5.0g Yeast extract........................................................5.0g Glucose ...............................................................2.0g NaCl....................................................................2.0g MgSO4·7H2O solution .................................... 0.2mL
Preparation of Egg Yolk Agar Base: Add components to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C.
MgSO4·7H2O Solution: Composition per 100.0mL: MgSO4·7H2O ......................................................5.0g
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Clostridium difficile Agar
Preparation of MgSO4·7H2O Solution: Add MgSO4·7H2O to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Cycloserine Solution: Composition per 100.0mL: Cycloserine .........................................................1.0g
Preparation of Cycloserine Solution: Add cycloserine to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Sulfamethoxazole Solution: Composition per 100.0mL: Sulfamethoxazole................................................1.9g
Preparation of Sulfamethoxazole Solution: Add sulfamethoxazole to distilled/deionized water and bring volume to 50.0mL. Add sufficient 10% NaOH to dissolve. Bring volume to 100.0mL with distilled/ deionized water. Mix thoroughly. Filter sterilize.
Trimethoprim Solution: Composition per 100.0mL: Trimethoprim ......................................................0.1g
Preparation of Trimethoprim Solution: Add trimethoprim to distilled/deionized water and bring volume to 50.0mL. Gently heat to 55°C. Add sufficient 0.05N HCl to dissolve. Bring volume to 100.0mL with distilled/deionized water. Mix thoroughly. Filter sterilize.
Egg Yolk Emulsion, 50%: Composition per 100.0mL: Chicken egg yolks..................................................11 Whole chicken egg...................................................1 NaCl (0.9% solution) .................................... 50.0mL
Preparation of Egg Yolk Emulsion, 50%:
species and Clostridium botulinum type G appear as pinpoint colonies with no opaque zone.
Clostridium difficile Agar Composition per liter: Clostridum difficile agar base ..................... 920.0mL Horse blood, defibrinated ............................. 70.0mL Clostridium difficile selective supplement .............................. 10.0mL pH 7.4 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath.
Clostridum difficile Agar Base: Composition per 920.0mL: Proteose peptone...............................................40.0g Agar ..................................................................15.0g Fructose...............................................................6.0g Na2HPO4 .............................................................5.0g NaCl....................................................................2.0g KH2PO4...............................................................1.0g MgSO4·7H2O ......................................................0.1g
Preparation of Clostridum difficile Agar Base: Add components to distilled/deionized water and bring volume to 920.0mL. Mix thoroughly. Gently heat to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Clostridium difficile Selective Supplement: Composition per 10.0mL: D-Cycloserine ...............................................500.0mg
Cefoxitin ........................................................16.0mg
Preparation of Clostridium difficile Selective Supplement: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Soak eggs with 1:100 dilution of saturated mercuric chloride solution for 1 min. Crack eggs and separate yolks from whites. Mix egg yolks with 1 chicken egg. Beat to form emulsion. Measure 50.0mL of egg yolk emulsion and add to 50.0mL of 0.9% NaCl solution. Mix thoroughly. Filter sterilize. Warm to 45°–50°C.
Preparation of Medium: Add 10.0mL of sterile Clostridium difficile selective supplement and 70.0mL of sterile, defibrinated horse blood to 920.0mL of cooled, sterile Clostridum difficile agar base. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Preparation of Medium: Aseptically add warmed, sterile egg yolk emulsion, 50%, and sterile cycloserine solution, sterile sulfamethoxazole solution, and sterile trimethoprim solution to cooled, sterile egg yolk agar base. Mix thoroughly. Pour into sterile Petri dishes.
Use: For the selective isolation and cultivation of
Use: For isolation, cultivation, and differentiation based on lipase activity of Clostridium botulinum types A, B, and F from fecal specimens associated with foodborne and infant botulism. Clostridium botulinum types A, B, and F appear as raised colonies surrounded by an opaque zone. Other Clostridium
Clostridium difficile from clinical and nonclinical specimens.
Clostridium difficile Agar (Cycloserine Cefoxitin Fructose Agar) (CCFA) Composition per liter: Peptic digest of animal tissue ...........................32.0g Agar ..................................................................20.0g Fructose...............................................................6.0g
Clostridium Medium Na2HPO4 .............................................................5.0g NaCl ....................................................................2.0g KH2PO4 ...............................................................1.0g Cycloserine .......................................................0.25g MgSO4 ................................................................0.1g Neutral Red .......................................................0.03g Cefoxitin solution ......................................... 10.0mL pH 7.2 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Cefoxitin Solution: Composition per 10.0mL: Cefoxitin ........................................................16.0mg
Preparation of Cefoxitin Solution: Add cefoxitin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 10.0mL of sterile cefoxitin solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the selective isolation and cultivation of Clostridium difficile from clinical and nonclinical specimens.
Clostridium Medium Composition per liter: Sodium L-glutamate ..........................................10.0g Sodium thioglycolate ..........................................0.5g Yeast extract........................................................0.5g K2HPO4 ...............................................................0.2g MgSO4·7H2O ......................................................0.1g pH 7.6 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the enrichment and isolation of glutamatefermenting Clostridium species.
Clostridium Medium Composition per liter: Uric acid..............................................................2.0g Yeast extract........................................................1.2g MgSO4·7H2O ....................................................0.05g CaCl2·2H2O......................................................5.0mg FeSO4·7H2O.....................................................2.0mg Resazurin .........................................................1.0mg KOH (10N solution)........................................ 3.0mL
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K2HPO4·3H2O (70% solution) ....................... 1.5mL Mercaptoacetic acid ........................................ 1.5mL pH 7.2 ± 0.2 at 25°C
Preparation of Medium: Add KOH solution and K2HPO4·3H2O solution to distilled/deionized water and bring volume to 500.0mL. Gently heat and bring to boiling. Mix thoroughly. Add uric acid slowly. Cool to 45°–50°C. Add remaining components. Add mercaptoacetic acid immediately prior to sterilization. Bring volume to 1.0L with distilled/deionized water. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Adjust pH to 7.2 with sterile 60% K2CO3 solution.
Use: For the isolation and cultivation of purine-fermenting Clostridium species.
Clostridium Medium (ATCC Medium 39) Composition per liter: K2HPO4...............................................................7.0g γ-Aminobutyric acid ...........................................5.0g Yeast extract........................................................3.0g Agar ....................................................................1.5g KH2PO4...............................................................1.3g MgCl2·6H2O .......................................................0.2g CaCl2·2H2O ......................................................0.01g FeCl3·6H2O .......................................................0.01g Methylene Blue................................................2.0mg MnSO4 .............................................................1.0mg Na2MoO4 .........................................................1.0mg Na2S·9H2O solution...................................... 10.0mL
Na2S·9H2O Solution: Composition per 20.0mL: Na2S·9H2O .........................................................0.6g
Preparation of Na2S·9H2O Solution: Add
Na2S·9H2O to distilled/deionized water and bring volume to 20.0mL. Autoclave for 15 min at 15 psi pressure–121°C. Use freshly prepared solution.
Preparation of Medium: Add components, except Na2S·9H2O, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C. Distribute anaerobically into sterile tubes. Aseptically add 0.1mL of sterile 1.5% Na2S·9H2O solution to each 5.0mL of the medium. Cap with rubber stoppers.
Use: For the cultivation and maintenance of a variety of Clostridium species.
Clostridium Medium (ATCC Medium 40) Composition per liter: K2HPO4...............................................................7.0g
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Clostridium Medium
δ-Aminovaleric acid·HCl (neutralized) ..............5.0g Agar ....................................................................1.5g KH2PO4 ...............................................................1.3g Yeast extract........................................................1.0g MgCl2·6H2O .......................................................0.2g CaCl2·2H2O.......................................................0.01g FeCl3·6H2O .......................................................0.01g Methylene Blue................................................2.0mg MnSO4 .............................................................1.0mg Na2MoO4 .........................................................1.0mg Na2S·9H2O solution...................................... 20.0mL
Preparation of Medium: Add components, except Na2S·9H2O solution, to tap water and bring volume to 1.0L. Mix thoroughly. Gently heat to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Distribute anaerobically into sterile tubes. Aseptically add 0.15mL of sterile Na2S·9H2O solution to each 5.0mL of the medium. Cap with rubber stoppers.
Use: For the cultivation and maintenance of a variety of Clostridium species.
Clostridium Medium (ATCC Medium 163)
Na2S·9H2O Solution: Composition per 100.0mL: Na2S·9H2O..........................................................1.5g
Composition per liter:
Preparation of Na2S·9H2O Solution: Add
Agar ..................................................................20.0g Sodium glutamate .............................................17.0g Yeast extract........................................................6.0g Sodium thioglycolate ..........................................0.5g Phosphate buffer (1.0M, pH 7.4) .................. 40.0mL MgSO4 (2.0M solution) .................................. 0.5mL FeSO4 (0.2M solution) .................................... 0.2mL CaCl2 (1.0M solution)..................................... 0.1mL CoCl2 (0.1M solution)..................................... 0.1mL MnCl2 (0.1M solution).................................... 0.1mL Na2MoO4 (0.1M solution) .............................. 0.1mL
Na2S·9H2O to distilled/deionized water and bring volume to 100.0mL. Autoclave for 15 min at 15 psi pressure–121°C. Use freshly prepared solution.
Preparation of Medium: Add components, except Na2S·9H2O solution, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Distribute anaerobically into sterile tubes. Aseptically add 0.1mL of sterile Na2S·9H2O solution to each 5.0mL of the medium. Cap with rubber stoppers.
Use: For the cultivation and maintenance of a variety of Clostridium species.
Clostridium Medium (ATCC Medium 43) Composition per liter: Agar ..................................................................15.0g Yeast extract........................................................5.0g L-Arginine·HCl....................................................2.0g L-Lysine·HCl .......................................................2.0g NH4Cl .................................................................2.0g Sodium formate...................................................2.0g K2HPO4 .............................................................1.75g MgSO4·7H2O ......................................................0.2g CaCl2·2H20 .......................................................0.01g FeSO4·7H2O......................................................0.01g Methylene Blue................................................2.0mg Na2S·9H2O solution...................................... 30.0mL
Na2S·9H2O Solution: Composition per 100.0mL: Na2S·9H2O..........................................................1.0g
Preparation of Na2S·9H2O Solution: Add
Na2S·9H2O to distilled/deionized water and bring volume to 100.0mL. Autoclave for 15 min at 15 psi pressure–121°C. Use freshly prepared solution.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation and maintenance of a variety of Clostridium species.
Clostridium Medium (ATCC Medium 511) Composition per liter: Yeast extract........................................................4.0g Alanine................................................................3.0g Peptone ...............................................................3.0g L-Cysteine ...........................................................0.2g MgSO4 ..............................................................0.05g FeSO4 ................................................................0.01g Potassium phosphate buffer (1.0M, pH 7.1) .............................. 5.0mL CaSO4 (saturated solution) ............................. 2.5mL
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of a variety of Clostridium species.
Clostridium novyi Blood Agar
Clostridium Medium (ATCC Medium 568) Composition per liter: Na2CO3 .............................................................10.0g Fructose...............................................................3.0g K2HPO4 ...............................................................2.0g Yeast extract........................................................2.0g (NH4)2SO4...........................................................1.0g MgSO4·7H2O ......................................................0.5g Sodium thioglycolate ........................................0.05g CaSO4 .............................................................0.015g FeSO4·7H2O.....................................................2.5mg MnSO4·H2O .....................................................0.5mg Na2MoO4·2H2O ...............................................0.5mg pH 7.8 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of a variety of Clostridium species.
Clostridium Medium (ATCC Medium 591) Composition per liter: Solution 1.................................................... 600.0mL Solution 2.................................................... 400.0mL pH 8.0 ± 0.2 at 25°C
Solution 1: Composition per 600.0mL: Peptone................................................................5.0g
Preparation of Solution 1: Add component to distilled/deionized water and bring volume to 600.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C.
Solution 2: Composition per 400.0mL: NaHCO3 ............................................................20.0g Fructose.............................................................10.0g K2HPO4 .............................................................10.0g Sodium thioglycolate ........................................0.75g Vitamin solution............................................ 14.0mL Trace elements solution ................................ 10.0mL
Preparation of Solution 2: Add components, except sodium thioglycolate, to distilled/deionized water and bring volume to 400.0mL. Mix thoroughly. Gas with 100% CO2. Add sodium thioglycolate. Adjust pH to 8.0. Filter sterilize.
149
Nicotinic acid....................................................0.05g Pyridoxine.........................................................0.05g Pantothenic acid..............................................0.025g p-Aminobenzoic acid.......................................5.0mg Vitamin B12 ......................................................2.0mg Biotin ...............................................................1.0mg
Preparation of Vitamin Solution: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly.
Trace Elements Solution: Composition per liter: EDTA ..................................................................0.5g FeSO4·7H2O........................................................0.2g H3BO3 ...............................................................0.03g CoCl2·6H2O ......................................................0.02g ZnSO4·7H2O .....................................................0.01g MnCl2·4H2O ....................................................3.0mg Na2MoO4·2H2O ...............................................3.0mg NiCl2·6H2O ......................................................2.0mg CuCl2·2H2O .....................................................1.0mg
Preparation of Trace Elements Solution: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly.
Preparation of Medium: Aseptically combine 600.0mL of sterile solution 1 and 400.0mL of sterile solution 2. Distribute into sterile tubes or flasks.
Use: For the cultivation and maintenance of a variety of Clostridium species.
Clostridium novyi Blood Agar Composition per 100.0mL: Agar ....................................................................2.0g Glucose ...............................................................1.0g Neopeptone .........................................................1.0g Proteolyzed liver.................................................0.5g Yeast extract........................................................0.5g Horse blood, defibrinated ............................. 10.0mL Reducing solution ......................................... 0.75mL Salts solution................................................... 0.5mL pH 7.6–7.8 at 25°C
Salts Solution: Composition per 100.0mL: MgSO4·7H2O ......................................................4.0g MnSO4·4H2O ......................................................0.2g HCl....................................................................0.05g FeCl3 .................................................................0.04g
Preparation of Salts Solution: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly.
Vitamin Solution: Composition per 100.0mL:
Reducing Solution: Composition per 10.0mL:
Thiamine .............................................................0.1g
L-Cysteine·HCl·H2O .........................................0.12g
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Clostridium perfringens Agar, OPSP
Dithiothreitol.....................................................0.12g Glutamine..........................................................0.06g
add sterile antibiotic inhibitor. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Preparation of Reducing Solution: Add com-
Use: For the presumptive identification and enumer-
ponents to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Adjust pH to 7.6– 7.8. Filter sterilize.
Preparation of Medium: Add agar to distilled/ deionized water and bring volume to 50.0mL. Mix thoroughly. Gently heat and bring to boiling. In another flask, add neopeptone, yeast extract, liver extract, and salts solution to distilled/deionized water and bring volume to 50.0mL. Mix thoroughly. Gently heat until dissolved. Combine the two solutions. Distribute into screw-capped bottles in 18.0mL volumes. Autoclave for 10 min at 10 psi pressure–115°C. Cool to 45°–50°C. Medium may be stored at 4°C at this point. Immediately prior to inoculation, aseptically add 2.0mL of horse blood and 0.15mL of sterile reducing solution to each tube of melted agar at 50°C. Mix thoroughly. Pour the contents of each tube into a sterile Petri dish.
Use: For the cultivation of Clostridium novyi.
Clostridium perfringens Agar, OPSP (Perfringens Agar, OPSP) Composition per liter: Pancreatic digest of casein................................15.0g Agar ..................................................................10.0g Liver extract........................................................7.0g Papaic digest of soybean meal ............................5.0g Yeast extract........................................................5.0g Tris(hydroxymethyl)aminomethane buffer.........1.5g Ferric ammonium citrate.....................................1.0g Na2S2O5 ..............................................................1.0g Antibiotic inhibitor ....................................... 10.0mL pH 7.3 ± 0.2 at 25°C
ation of Clostridium perfringens.
Clostridium Selective Agar (Clostrisel Agar) Composition per liter: Pancreatic digest of casein................................17.0g Agar ..................................................................14.0g Glucose ...............................................................6.0g Papaic digest of soybean meal............................3.0g NaCl....................................................................2.5g Sodium thioglycolate ..........................................1.8g Sodium formaldehyde sulfoxylate......................1.0g L-Cystine ...........................................................0.25g NaN3 .................................................................0.15g Neomycin sulfate ..............................................0.15g pH 7.0 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–118°C. Pour into sterile Petri dishes or leave in tubes.
Caution: Sodium azide is toxic. Azides also react with metals and disposal must be highly diluted.
Use: For the selective isolation of pathogenic Clostridium species from specimens containing mixed flora, e.g., from wounds, fecal specimens, and other specimens.
CM3 Medium Composition per liter:
ponents to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
3–(N–Morpholino)propanesulfonic acid (MOPS) buffer ....................................20.0g Cellobiose (or Cellulose MN 300)....................10.0g K2HPO4...............................................................4.4g Urea.....................................................................1.5g L-Cysteine·HCl·H2O ...........................................1.0g MgSO4·7H2O ......................................................0.5g (NH4)2SO4 ..........................................................0.4g CaCl2·2H2O ......................................................0.05g FeSO4·7H2O.....................................................1.0mg pH 7.1 ± 0.2 at 25°C
Preparation of Medium: Add components, ex-
Preparation of Medium: Add components to
cept antibiotic inhibitor, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically
Use: For the cultivation of Clostridium species.
Source: This medium is available as a premixed powder from Oxoid Unipath. Antibiotic Inhibitor: Composition per 10.0mL: Sodium sulfadiazine............................................0.1g Oleandomycin phosphate.................................0.5mg Polymyxin B ................................................10,000U
Preparation of Antibiotic Inhibitor: Add com-
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
COBA
CN Screen Medium (Cryptococcus neoformans Screen Medium) Composition per liter: Agar ..................................................................15.0g K2HPO4 ...............................................................4.0g MgSO4·7H2O ......................................................2.5g Glucose .............................................................1.25g Asparagine ..........................................................1.0g Glutamine............................................................1.0g Glycine................................................................1.0g Thiamine·HCl .....................................................1.0g Tryptophan ..........................................................1.0g EDTA ..................................................................0.6g Biotin ................................................................0.51g Dihydroxyphenylalanine (Dopa) ........................0.2g Phenol Red..........................................................0.2g pH 5.5–5.6 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat until boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the screening of yeast isolates for the presumptive identification of Cryptococcus neoformans. Cryptococcus neoformans forms black colonies.
Coagulase Agar Base Composition per liter: Agar ..................................................................25.0g Brain heart infusion ..........................................10.5g Pancreatic digest of casein................................10.5g D-Mannitol ........................................................10.0g Brain heart infusion ............................................5.0g NaCl ....................................................................3.5g Papaic digest of soybean meal ............................3.5g Bromcresol Purple ............................................0.02g Rabbit plasma ............................................. 100.0mL pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components, except rabbit plasma, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat, while stirring, until boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C. Add rabbit plasma to a final concentration of 7–15%. Mix thoroughly. Pour into sterile Petri dishes in 18.0mL volume per plate.
Use: For the cultivation and differentiation of Staphylococcus aureus from other Staphylococcus species based on coagulase production.
151
Coagulase Mannitol Agar Composition per liter: Agar ..................................................................14.5g Pancreatic digest of casein................................10.5g D-Mannitol ........................................................10.0g Brain heart infusion ............................................5.0g NaCl....................................................................3.5g Papaic digest of soybean meal............................3.5g Bromcresol Purple ............................................0.02g Rabbit plasma with 0.15% EDTA............... 100.0mL pH 7.3 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components, except rabbit plasma, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring until boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C. Add rabbit plasma with 0.15% EDTA to a final concentration of 7–15%. Mix thoroughly. Pour into sterile Petri dishes in 18.0mL volume per plate.
Use: For the cultivation and differentiation of Staphylococcus aureus from other Staphylococcus species based on coagulase production and mannitol fermentation.
COBA (Colistin Oxolinic Acid Blood Agar) Composition per liter: Columbia agar base..................................... 930.0mL Horse blood, defibrinated, sterile.................. 50.0mL Colistin sulfate solution ................................ 10.0mL Oxolinic acid solution................................... 10.0mL pH 7.3 ± 0.2 at 25°C
Columbia Agar Base: Composition per 930.0mL: Agar ..................................................................13.5g Pancreatic digest of casein................................10.0g Peptic digest of animal tissue ...........................10.0g NaCl....................................................................5.0g Beef extract.........................................................3.0g Yeast extract........................................................3.0g Cornstarch...........................................................1.0g
Preparation of Columbia Agar Base: Add components to distilled/deionized water and bring volume to 930.0mL. Mix thoroughly. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C.
Colistin Sulfate Solution: Composition per 10.0mL: Colistin sulfate ...............................................10.0mg
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Coletsos Medium
Preparation of Colistin Sulfate Solution: Add colistin sulfate to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Distribute into sterile screw-capped tubes. Place tubes in a slanted position. Inspissate at 85°C (moist heat) for 45 min.
Oxolinic Acid Solution: Composition per 10.0mL:
Use: For the cultivation of Mycobacterium tuberculosis.
Oxolinic acid...........................................5.0–10.0mg
Preparation of Oxolinic Acid Solution: Add oxolinic acid to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: To 930.0mL of sterile, cooled Columbia agar base, add sterile colistin sulfate, sterile oxolinic acid, and sterile, defibrinated horse blood. Mix thoroughly. Pour into sterile Petri dishes.
Use: For the isolation and cultivation of streptococci in pure culture from mixed flora in clinical specimens.
Coletsos Medium Composition per 1625mL: Potato starch......................................................10.0g Gelatin.................................................................4.0g Asparagine ........................................................2.25g KH2PO4 ...............................................................1.5g Na-glutamate.......................................................1.0g Na-pyruvate ........................................................1.0g Mg-citrate........................................................0.375g Litmus ...............................................................0.25g Malachite green.................................................0.25g MgSO4 ..............................................................0.15g Activated carbon .................................................0.1g Oligonucleotide mixture ..................................3.0mg Egg mixture................................................ 625.0mL Glycerol .......................................................... 7.5mL
Egg Mixture: Composition per liter: Whole eggs ......................................................18–24
Preparation of Egg Mixture: Use fresh eggs, less than 1 week old. Scrub the shells with soap. Let stand in a soap solution for 30 min. Rinse in running water. Soak eggs in 70% ethanol for 15 min. Break the eggs into a sterile container. Separate egg whites from egg yolks. Combine 8 parts egg white with 2 parts egg yolk. Homogenize by shaking. Filter through four layers of sterile cheesecloth into a sterile graduated cylinder. Bring volume to 1.0L distilled/deionized water.
Preparation of Medium: Add glycerol to 600.0mL of distilled/deionized water. Mix thoroughly. Add remaining components, except egg mixture. Bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C. Aseptically add 625.0mL of egg mixture. Mix thoroughly.
Coletsos Selective Medium Composition per 1625mL: Potato starch......................................................10.0g Gelatin.................................................................4.0g Asparagine ........................................................2.25g KH2PO4...............................................................1.5g Na-glutamate.......................................................1.0g Na-pyruvate ........................................................1.0g Mg-citrate .......................................................0.375g Litmus ...............................................................0.25g Malachite green ................................................0.25g MgSO4 ..............................................................0.15g Activated carbon.................................................0.1g Oligonucleotide mixture ..................................3.0mg Homogenized egg ...................................... 625.0mL Glycerol .......................................................... 7.5mL Nalidixic acid solution.................................... 1.0mL Lincomycin solution ....................................... 1.0mL Cycloheximide solution .................................. 1.0mL
Nalidixic Acid Solution: Composition per 100.0mL: Nalidixic acid......................................................0.5g
Preparation of Nalidixic Acid Solution: Add nalidixic acid to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize. Cycloheximide Solution: Composition per 100.0mL: Cycloheximide....................................................1.5g Ethanol.......................................................... 40.0mL
Preparation of Cycloheximide Solution: Add cycloheximide to 40.0mL of ethanol. Mix thoroughly. Bring volume to 100.0mL with distilled/deionized water. Filter sterilize. Lincomycin Solution: Composition per 100.0mL: Lincomycin .........................................................0.5g
Preparation of Lioncomycin Solution: Add lincomycin to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize. Egg Mixture Solution: Composition per liter: Whole eggs ......................................................18–24
Preparation of Egg Mixture Solution: Use fresh eggs, less than 1 week old. Scrub the shells with soap. Let stand in a soap solution for 30 min. Rinse
Coliform Agar ES, Chromocult in running water. Soak eggs in 70% ethanol for 15 min. Break the eggs into a sterile container. Separate egg whites from egg yolks. Combine 8 parts egg white with 2 parts egg yolk. Homogenize by shaking. Filter through four layers of sterile cheesecloth into a sterile graduated cylinder. Bring volume to 1.0L distilled/deionized water.
Preparation of Medium: Add glycerol to 600.0mL of distilled/deionized water. Mix thoroughly. Add remaining components, except egg mixture, lincomycin solution, cycloheximide solution, and nalidixic acid solution. Mix thoroughly. Bring volume to 1.0L. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C. Aseptically add 625.0mL of egg mixture. Mix thoroughly. Aseptically add 1.0mL cycloheximide solution, 1.0mL lincomycin solution, and 1.0mL nalidixic acid solution. Distribute into sterile screw-capped tubes. Place tubes in a slanted position. Inspissate at 85°C (moist heat) for 45 min.
Use: For the isolation and cultivation of Mycobacterium tuberculosis.
Coliform Agar, Chromocult® (Chromocult Coliform Agar) Composition per liter: Agar ..................................................................10.0g NaCl ....................................................................5.0g Peptone................................................................3.0g Na2HPO4 .............................................................2.7g NaH2PO4 .............................................................2.2g Tryptophan ..........................................................1.0g Na-pyruvatge ......................................................1.0g Chromogenic mixture .........................................0.4g Tergiotol 7.........................................................0.15g pH 7.0 ± 0.2 at 25°C
Source: This medium is available from Merck. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix well and warm gently until dissolved. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes. Some turbidity may occur, but this does not effect the performance
Use: For the detection of E. coli and coliform bacteria. The interaction of selected peptones, pyruvate, sorbitol, and phosphate buffer guarantees rapid colony growth, even for sublethally injured coliforms. The growth of Gram-positive bacteria as well as some Gram-negative bacteria is largely inhibited by the content of Tergitol 7 which has no negative effect on the growth of the coliform bacteria. A combination of two chromogenic substrates which allow for the simultaneous detection of total coliforms and E.
153
coli. The characteristic enzyme for coliforms, β-Dgalactosidase cleaves the Salmon-GAL substrate and causes a salmon to red color of the coliform colonies. The substrate X-glucuronide is used for the identification of β-D-glucuronidase, which is characteristic for E. coli. E. coli cleaves both Salmon-GAL and Xglucuronide, so that positive colonies take on a darkblue to violet color. These are easily distinguished from other coliform colonies which have a salmon to red color. As part of an additional confirmation of E. coli, the inclusion of tryptophan improves the indole reaction, thereby increasing detection reliability when it is used in combination with the Salmon-GAL and X-glucuronide reaction.
Coliform Agar ES, Chromocult (Chromocult Coliform Agar ES) (Chromocult Enhanced Selectivity Agar) Composition per liter: Agar ..................................................................10.0g MOPS ...............................................................10.0g KCl......................................................................7.5g Peptone ..............................................................5.0g Bile salts............................................................1.15g Na-propionate .....................................................0.5g 6-Chloro-3-indoxyl-β-D-galactopyranoside ....0.15g 5-Bromo-4-chloro-3-indoxylβ-D-glucuronic acid .....................................0.1g Isopropyl-β-D-thiogalactopyranoside ................0.1g pH 7.0 ± 0.2 at 25°C
Source: This medium is available from Merck. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly and heat with frequent agitation until components are completely dissolved (approximately 45 min.). Do not autoclave. Cool to 45°–50°C. Pour into sterile Petri dishes. The plates should be clear and colorless.
Use: For the detection of E.coli and total coliforms. The combination of suitable peptones and the buffering using MOPS allow rapid growth of coliforms and an optimal transformation of the chromogenic substrates. The amount of bile salts and propionate largely inhibit growth of Gram-positive and Gram-negative accompanying flora. The simultaneous detection of total coliforms and E.coli is achieved using the combination of two chromogrenic substrates. The substrate Salmon™--β-D-GAL is split by β-D-galactosidase, characteristic for coliforms, resulting in a salmon to red coloration of coliform colonies. The detection of the β-D-glucuronidase, characteristic for E.coli, is cleaved via the substrate X-β-D-glucu-
154
Columbia Agar
ronide, causing a blue coloration of positive colonies. As E.coli splits Salmon-β-D-GAL as well as X-β-Dglucuronide, the colonies turn to a dark violet color and can be easily differentiated from the other coliforms being salmon-red.
Columbia Agar Composition per liter: Columbia agar base..................................... 950.0mL Sheep blood................................................... 50.0mL pH 7.3 ± 0.2 at 25°C
Columbia Agar Base: Composition per liter: Agar ..................................................................13.5g Pancreatic digest of casein................................12.0g NaCl ....................................................................5.0g Peptic digest of animal tissue..............................5.0g Beef extract .........................................................3.0g Yeast extract........................................................3.0g Cornstarch...........................................................1.0g
Preparation of Columbia Agar Base: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C.
Preparation of Medium: To 950.0mL of cooled, sterile Columbia agar base, aseptically add 50.0mL of sterile, defibrinated sheep blood. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation and cultivation of nonfastidious and fastidious microorganisms from a variety of clinical and nonclinical specimens.
Columbia Blood Agar Composition per liter: Columbia blood agar base........................... 950.0mL Sheep blood................................................... 50.0mL pH 7.3 ± 0.2 at 25°C
Columbia Blood Agar Base: Composition per liter: Agar ..................................................................15.0g Pantone..............................................................10.0g Bitone................................................................10.0g NaCl ....................................................................5.0g Tryptic digest of beef heart .................................3.0g Cornstarch...........................................................1.0g
Source: Columbia blood agar base is available as a premixed powder from BD Diagnostic Systems.
Preparation of Columbia Blood Agar Base: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat
until boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Preparation of Medium: To 950.0mL of cooled, sterile Columbia blood agar base, aseptically add 50.0mL of sterile, defibrinated sheep blood. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: With the addition of blood or other enrichments, used for the isolation and cultivation of fastidious microorganisms.
Columbia Blood Agar (DSMZ Medium 693) Composition per liter: Columbia blood agar base .......................... 950.0mL Sheep blood .................................................. 50.0mL pH 7.3 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath.
Columbia Blood Agar Base: Composition per liter: Special peptone.................................................23.0g Agar ..................................................................10.0g NaCl....................................................................5.0g Starch ..................................................................1.0g
Preparation of Columbia Blood Agar Base: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Preparation of Medium: To 950.0mL of cooled, sterile Columbia blood agar base, aseptically add 50.0mL of sterile, defibrinated sheep blood. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation of Corynebacterium spp., Actinomyces spp., Arcanobacterium spp., Streptococcus pneumoniae, Lactobacillus iners, Isobaculum melis, Nocardia paucivorans, and a variety of fastidious microorganisms.
Columbia Blood Agar Base Composition per liter: Agar ..................................................................15.0g Pantone .............................................................10.0g Bitone................................................................10.0g NaCl....................................................................5.0g Tryptic digest of beef heart.................................3.0g Cornstarch...........................................................1.0g
Source: Columbia blood agar base is available as a premixed powder from BD Diagnostic Systems.
Columbia Broth Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation of Balneatrix alpica.
Columbia Blood Agar Base with Horse Blood (LMG Medium 151) Composition per liter: Columbia blood agar base........................... 950.0mL Horse blood................................................... 50.0mL pH 7.3 ± 0.2 at 25°C
Columbia Blood Agar Base: Composition per liter: Special peptone .................................................23.0g Agar ..................................................................10.0g NaCl ....................................................................5.0g Starch ..................................................................1.0g
Preparation of Columbia Blood Agar Base: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Preparation of Medium: To 950.0mL of cooled, sterile Columbia blood agar base, aseptically add 50.0mL of sterile, defibrinated horse blood. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation of Arcanobacterium spp., Paenibacillus spp., Corynebacterium spp., Lactobacillus iners, Enterococcus spp. and other bacteria.
Columbia Blood Agar Base with Horse Blood (LMG Medium 210) Composition per liter:
155
bring volume to 1.0L. Mix thoroughly. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Preparation of Medium: To 950.0mL of cooled, sterile Columbia blood agar base, aseptically add 50.0mL of sterile, defibrinated horse blood. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation of Actinomyces spp., Streptococcus dysgalactiae, and Actinobaculum spp.
Columbia Blood Agar Base with Horse Blood and Charcoal (DSMZ Medium 429a) Composition per liter: Columbia blood agar base with charcoal.... 960.0mL Horse blood................................................... 40.0mL pH 7.3 ± 0.2 at 25°C
Columbia Blood Agar Base with Charcoal: Composition per liter: Agar ..................................................................15.0g Pancreatic digest of casein................................10.0g Proteose peptone no. 3........................................5.0g Yeast extract........................................................5.0g NaCl....................................................................5.0g Beef heart digest .................................................3.0g Charcoal..............................................................2.0g Corn starch..........................................................1.0g
Preparation of Columbia Blood Agar Base with Charcoal: Add components to distilled/ deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Preparation of Medium: To 960.0mL of cooled, sterile Columbia blood agar base, aseptically add 40.0mL of sterile, defibrinated horse blood. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Columbia blood agar base........................... 950.0mL Horse blood................................................... 50.0mL pH 7.3 ± 0.2 at 25°C
Use: For the cultivation of Neisseria gonorrhoeae.
Columbia Blood Agar Base: Composition per liter:
Composition per liter:
Agar ..................................................................15.0g Pancreatic digest of casein................................10.0g Proteose peptone no. 3 ........................................5.0g Yeast extract........................................................5.0g NaCl ....................................................................5.0g Beef heart digest .................................................3.0g Corn starch..........................................................1.0g
Preparation of Columbia Blood Agar Base: Add components to distilled/deionized water and
Columbia Broth Bitone................................................................10.0g Pancreatic digest of casein..................................5.0g Peptic digest of animal tissue .............................5.0g NaCl....................................................................5.0g Tryptic digest of beef heart.................................3.0g Tris(hydroxymethyl)aminomethane·HCl..........2.86g Glucose ...............................................................2.5g Tris(hydroxymethyl)aminomethane .................0.83g Na2CO3 ...............................................................0.6g L-Cysteine·HCl....................................................0.1g
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Columbia Broth
MgSO4, anhydrous..............................................0.1g FeSO4 ................................................................0.02g pH 7.5 ± 0.2 at 25°C
Columbia Blood Agar Base: Composition per liter:
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat until boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Agar ..................................................................13.5g Pancreatic digest of casein................................12.0g NaCl....................................................................5.0g Peptic digest of animal tissue .............................5.0g Beef extract.........................................................3.0g Yeast extract........................................................3.0g Cornstarch...........................................................1.0g Nalidixic acid.................................................15.0mg Colistin...........................................................10.0mg
Use: For the cultivation and isolation of fastidious
Preparation of Columbia Blood Agar Base:
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to
bacteria from clinical specimens or as a general purpose broth.
Columbia Broth Composition per liter: Pancreatic digest of casein................................10.0g Peptic digest of animal tissue..............................8.0g NaCl ....................................................................5.0g Yeast extract........................................................5.0g Tris(hydroxymethyl) aminomethane·HCl buffer ..........................2.86g Glucose ...............................................................2.5g Tris(hydroxymethyl) aminomethane buffer..................................0.83g L-Cysteine·HCl·H2O ...........................................0.1g MgSO4·7H2O ....................................................0.05g FeSO4 ..............................................................0.012g pH 7.4 ± 0.2 at 25°C
Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Preparation of Medium: To 950.0mL of cooled, sterile Columbia blood agar base, aseptically add 50.0mL of sterile, defibrinated sheep blood. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes. Use: For the selective isolation, cultivation, and differentiation of Gram-positive cocci from clinical and nonclinical specimens.
Columbia CNA Agar, Modified with Sheep Blood Composition per liter: Columbia blood agar base .......................... 950.0mL Sheep blood, defribinated ............................. 50.0mL pH 7.3 ± 0.2 at 25°C
Source: This medium is available as a premixed
Source: This medium is available as a premixed
powder from BD Diagnostic Systems.
powder from BD Diagnostic Systems.
Columbia Blood Agar Base: Composition per liter:
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat until boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of a wide variety of microorganisms. Used as a general purpose medium.
Columbia CNA Agar (Columbia Colistin Nalidixic Acid Agar) Composition per liter: Columbia blood agar base.............................. 950.0L Sheep blood................................................... 50.0mL pH 7.3 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Agar ..................................................................13.5g Pancreatic digest of casein................................12.0g NaCl....................................................................5.0g Peptic digest of animal tissue .............................5.0g Beef extract.........................................................3.0g Yeast extract........................................................3.0g Cornstarch...........................................................1.0g Colistin...........................................................10.0mg Nalidixic acid...................................................5.0mg
Preparation of Columbia Blood Agar Base: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Preparation of Medium: To 950.0L of cooled, sterile Columbia blood agar base, aseptically add 50.0mL of sterile, defibrinated sheep blood. Mix
Congo Red Agar thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
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Congo Red Agar (CR Agar)
Use: For the selective isolation, cultivation, and dif-
Composition per liter:
ferentiation of Gram-positive cocci from clinical and nonclinical materials.
GC agar base............................................... 890.0mL Hemoglobin solution .................................. 100.0mL Supplement solution ..................................... 10.0mL Congo Red (0.01% solution) .......................... 0.1mL pH 7.2 ± 0.2 at 25°C
Complex Medium Composition per liter: NaCl ................................................................250.0g MgSO4·7H2O ....................................................20.0g Yeast extract......................................................10.0g Casamino acids ...................................................7.5g Trisodium citrate .................................................3.0g KCl......................................................................2.0g pH 7.5–7.8 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Autoclave for 5 min at 15 psi pressure–121°C. Filter through Whatman #1 filter paper. Adjust pH of filtrate to 7.4. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure– 121°C.
Use: For the isolation and cultivation of Actinomadura species, Actinopolyspora species, Excellospora species, and Microspora species.
Congo Red Acid Morpholinepropanesulfonic Acid Pigmentation Agar (CRAMP Agar) Composition per liter: Agarose .............................................................14.0g Morpholinepropanesulfonic acid ........................8.4g NaCl ....................................................................2.9g Casamino acids ...................................................2.0g Galactose.............................................................2.0g Tricine (n-Tris-hydroxymethylmethylglycine) buffer ...................................1.8g Na2S2O3·5H2O ....................................................0.6g NH4Cl .................................................................0.5g K2HPO4 .............................................................0.24g MgSO4·7H2O ......................................................0.1g Congo Red .......................................................5.0mg pH 5.3 ± 0.2 at 25°C
GC Agar Base: Composition per 890.0mL: Agar ..................................................................10.0g Pancreatic digest of casein..................................7.5g Peptic digest of animal tissue .............................7.5g NaCl....................................................................5.0g K2HPO4...............................................................4.0g Cornstarch...........................................................1.0g KH2PO4...............................................................1.0g
Preparation of GC Agar Base: Add components to distilled/deionized water and bring volume to 890.0mL. Mix thoroughly. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Hemoglobin Solution: Composition per 100.0mL: Hemoglobin ........................................................2.0g
Preparation of Hemoglobin Solution: Add hemoglobin to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C.
Congo Red Solution: Composition per 100.0mL: Congo Red ........................................................0.01g
Preparation of Congo Red Solution: Add Congo Red to 100.0mL of distilled/deionized water. Mix thoroughly. Autoclave for 15 min at 15 psi pressure– 121°C.
Supplement Solution: Composition per liter:
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Adjust pH to 5.3. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Glucose ...........................................................100.0g L-Cysteine·HCl..................................................25.9g L-Glutamine ......................................................10.0g L-Cystine .............................................................1.1g Adenine...............................................................1.0g Nicotinamide adenine dinucleotide ..................0.25g Vitamin B12 .........................................................0.1g Thiamine pyrophosphate ....................................0.1g Guanine·HCl .....................................................0.03g Fe(NO3)3·6H2O.................................................0.02g p-Aminobenzoic acid......................................0.013g Thiamine·HCl ..................................................3.0mg
Use: For the cultivation of Yersinia species with
Source: The supplement solution IsoVitaleX en-
plasmids.
richment is available from BD Diagnostic Systems.
Preparation of Medium: Add components to
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Congo Red Agar
This enrichment may be replaced by supplement VX from BD Diagnostic Systems.
Preparation of Supplement Solution: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
Preparation of Medium: To 890.0mL of sterile, cooled GC agar base aseptically add 100.0mL of sterile, cooled hemoglobin solution, 10.0mL of sterile supplement solution, and 0.1mL of sterile Congo Red solution. Mix thoroughly. Pour into sterile Petri dishes.
Use: For the isolation and differentiation of virulent and avirulent strains of Shigella, Vibrio cholerae, Escherichia coli, and Neisseria meningitidis. Used for the detection and differentiation of “iron-responsive” avirulent mutants. Used in the preparation of live vaccines. Used for the differentiation of sensitive Neisseria gonorrhoeae (no growth) from other Neisseria species (growth) that are resistant to Congo Red.
Congo Red Agar (CR Agar) Composition per liter: Soybean-casein digest agar......................... 890.0mL Hemoglobin solution................................... 100.0mL Supplement solution ..................................... 10.0mL Congo Red (0.01% solution) .......................... 0.1mL pH 7.3 ± 0.2 at 25°C
Soybean-Casein Digest Agar: Composition per 890.0mL: Pancreatic digest of casein................................17.0g Agar ..................................................................15.0g NaCl ....................................................................5.0g Papaic digest of soybean meal ............................3.0g Glucose ...............................................................2.5g K2HPO4 ...............................................................2.5g
Preparation of Soybean-Casein Digest Agar: Add components to distilled/deionized water and bring volume to 890.0mL. Mix thoroughly. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Hemoglobin Solution: Composition per 100.0mL: Hemoglobin ........................................................2.0g
Preparation of Hemoglobin Solution: Add hemoglobin to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C.
Congo Red Solution: Composition per 100.0mL: Congo Red ........................................................0.01g
Preparation of Congo Red Solution: Add Congo Red to 100.0mL of distilled/deionized water. Mix thoroughly. Autoclave for 15 min at 15 psi pressure– 121°C.
Supplement Solution: Composition per liter: Glucose ...........................................................100.0g L-Cysteine·HCl..................................................25.9g L-Glutamine ......................................................10.0g L-Cystine .............................................................1.1g Adenine...............................................................1.0g Nicotinamide adenine dinucleotide ..................0.25g Vitamin B12 .........................................................0.1g Thiamine pyrophosphate ....................................0.1g Guanine·HCl .....................................................0.03g Fe(NO3)3·6H2O.................................................0.02g p-Aminobenzoic acid......................................0.013g Thiamine·HCl ..................................................3.0mg
Preparation of Supplement Solution: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
Source: The supplement solution IsoVitaleX enrichment is available from BD Diagnostic Systems. This enrichment may be replaced by supplement VX from BD Diagnostic Systems.
Preparation of Medium: To 890.0mL of sterile, cooled soybean-casein digest agar, aseptically add 100.0mL of sterile, cooled hemoglobin solution, 10.0mL of sterile supplement solution, and 0.1mL of sterile Congo Red solution. Mix thoroughly. Pour into sterile Petri dishes.
Use: For the isolation and differentiation of virulent and avirulent strains of Shigella, Vibrio cholerae, Escherichia coli, and Neisseria meningitidis. Used for the detection and differentiation of “iron-responsive” avirulent mutants. Used in the preparation of live vaccines. Used for the differentiation of sensitive Neisseria gonorrhoeae (no growth) from other Neisseria species (growth) that are resistant to Congo Red.
Congo Red BHI Agarose Medium Composition per liter: Agarose .............................................................15.0g Pancreatic digest of gelatin...............................14.5g Brain heart, solids from infusion ........................6.0g Peptic digest of animal tissue .............................6.0g NaCl....................................................................5.0g Glucose ...............................................................3.0g Na2HPO4 .............................................................2.5g Congo Red ......................................................0.075g pH 7.4 ± 0.2 at 25°C
Conradi Drigalski Agar Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes in 20.0mL volumes.
Use: For the isolation, cultivation, and detection of virulent strains of Yersinia enterocolitica.
Congo Red BHI Agarose Medium (CRBHO Medium)
159
Agar ..................................................................15.0g Papaic digest of soybean meal............................5.0g NaCl....................................................................5.0g pH 7.3 ± 0.2 at 25°C
Preparation of Solution 1: Add components to distilled/deionized water and bring volume to 825.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Do not overheat.
Solution 2: Composition per liter:
Composition per liter:
MgCl2·6H2O .....................................................50.8g
Agarose .............................................................12.0g Pancreatic digest of gelatin ...............................14.5g Brain heart, solids from infusion ........................6.0g Peptic digest of animal tissue..............................6.0g NaCl ....................................................................5.0g Glucose ...............................................................3.0g Na2HPO4 .............................................................2.5g MgCl2 ..................................................................1.0g Congo Red solution ...................................... 20.0mL pH 7.4 ± 0.2 at 25°C
Preparation of Solution 2: Add MgCl2·6H2O to
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes in 20.0mL volumes.
Congo Red Solution: Composition per 100.0mL: Congo Red ...................................................375.0mg
Preparation of Congo Red Solution: Add Congo Red to 100.0mL of distilled/deionized water. Mix thoroughly. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 25°C.
Use: For the isolation, cultivation, and detection of virulent strains of Yersinia enterocolitica.
Congo Red Magnesium Oxalate Agar (CRMOX Agar) Composition per liter:
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C.
Solution 3: Composition per liter: Sodium oxalate .................................................33.2g
Preparation of Solution 3: Add sodium oxalate to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C.
Solution 4: Composition per 100.0mL: D-Galactose .......................................................20.0g
Preparation of Solution 4: Add
D-galactose to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Solution 5: Composition per 10.0mL: Congo Red ..........................................................0.1g
Preparation of Solution 5: Add Congo Red to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C.
Preparation of Medium: Aseptically combine 80.0mL of sterile solution 2, 80.0mL of sterile solution 3, 10.0mL of sterile solution 4, and 5.0mL of sterile solution 5. Mix thoroughly. Warm to 50°C. Add this mixture to 825.0mL of cooled, sterile solution 1. Mix thoroughly. Pour into sterile Petri dishes.
Solution 1.................................................... 825.0mL Solution 2...................................................... 80.0mL Solution 3...................................................... 80.0mL Solution 4...................................................... 10.0mL Solution 5........................................................ 5.0mL pH 7.3 ± 0.2 at 25°C
Use: For the cultivation and identification of patho-
Solution 1: Composition per 825.0mL:
Composition per liter:
Pancreatic digest of casein................................15.0g
genic serotypes of Yersinia enterocolitica. For the determination of whether Yersinia strains contain the Yersinia virulence plasmid.
Conradi Drigalski Agar Agar ..................................................................15.0g Casein ...............................................................10.0g
160
Converse Liquid Medium, Levine Modification
Lactose ..............................................................10.0g Peptone..............................................................10.0g NaCl ....................................................................5.0g Bromcresol Purple ............................................0.03g Crystal Violet ...................................................4.0mg pH 6.8 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat until boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the isolation and cultivation of Gram-negative enteric bacilli.
Converse Liquid Medium, Levine Modification Composition per liter: Ionagar no. 2 or Noble agar ..............................10.0g Glucose ...............................................................4.0g Ammonium acetate ...........................................1.23g K2HPO4 .............................................................0.52g Tamol ..................................................................0.5g MgSO4·7H2O ......................................................0.4g KH2PO4 ...............................................................0.4g NaCl ................................................................0.014g Na2CO3 ...........................................................0.012g CaCl2·2H2O.....................................................0.002g ZnSO4·7H2O ...................................................0.002g
Preparation of Medium: Add components to
tubes or flasks. Autoclave for 15 min at 15 psi pressure– 121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the isolation of fungi.
Cooked Meat Medium (LMG Medium 140) Composition per liter: Heart muscle ...................................................454.0g Peptone .............................................................40.0g Beef extract.......................................................10.0g NaCl....................................................................5.0g Yeast extract........................................................5.0g K2HPO4...............................................................5.0g Glucose ...............................................................2.0g Resazurin solution .......................................... 4.0mL pH 7.0 ± 0.2 at 25°C
Resazurin Solution: Composition per 100.0mL: Resazurin ........................................................0.025g
Preparation of Resazurin Solution: Add resazurin to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly.
Preparation of Medium: Finely chop beef heart. Add approximately 1.5g of heart particles to test tubes. Add remaining components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes in 10.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C. Slowly cool tubes to prevent expulsion of meat particles.
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes in 15.0mL volumes.
Use: For the cultivation and maintenance of Pep-
Use: For the cultivation and induction of spherules
Composition per liter:
of Coccidioides immitis.
Cooke Rose Bengal Agar Composition per liter: Agar ..................................................................20.0g Glucose .............................................................10.0g Enzymatic hydrolysate of soybean meal ............5.0g KH2PO4 ...............................................................1.0g MgSO4·7H2O ......................................................0.5g Rose Bengal ...................................................35.0mg pH 6.0 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat until boiling. Distribute into
tostreptococcus magnus.
Cooked Meat Medium Beef heart........................................................454.0g Proteose peptone...............................................20.0g NaCl....................................................................5.0g Glucose ...............................................................2.0g pH 7.2 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Finely chop beef heart. Add approximately 1.5g of heart particles to test tubes. Add remaining components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes in 10.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C. Slowly cool tubes to prevent expulsion of meat particles. Use: For the cultivation and maintenance of anaerobic microorganisms.
Cooked Meat Medium, Modified
Cooked Meat Medium
161
Source: This medium is available as a premixed
Composition per liter:
powder from BD Diagnostic Systems.
Heart muscle ...................................................454.0g Beef extract .......................................................10.0g Peptone..............................................................10.0g NaCl ....................................................................5.0g Glucose ...............................................................2.0g pH 7.2 ± 0.2 at 25°C
Preparation of Medium: Add approximately
Source: This medium is available as a premixed powder from Oxoid Unipath.
Preparation of Medium: Finely chop beef heart. Add approximately 1.5g of heart particles to test tubes. Add remaining components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes in 10.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C. Slowly cool tubes to prevent expulsion of meat particles.
Use: For the cultivation and maintenance of aerobic and anaerobic microorganisms. For the cultivation of anaerobes, especially pathogenic clostridia.
Cooked Meat Medium Composition per liter: Heart tissue granules.........................................98.0g Peptic digest of animal tissue............................20.0g NaCl ....................................................................5.0g Glucose ...............................................................2.0g pH 7.2 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add approximately 1.0g of heart tissue granules to test tubes. Add remaining components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes in 10.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C. Slowly cool tubes to prevent expulsion of meat particles.
Use: For the cultivation of anaerobes, especially pathogenic clostridia.
Cooked Meat Medium with Glucose, Hemin, and Vitamin K
1.0g of heart tissue granules to test tubes. Add remaining components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes in 10.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C. Slowly cool tubes to prevent expulsion of meat particles.
Use: For the cultivation of anaerobes, especially pathogenic clostridia.
Cooked Meat Medium, Modified Composition per tube: Cooked meat medium .........................................1.0g Diluent ............................................................... 1.0L pH 6.8 ± 0.2 at 25°C
Cooked Meat Medium: Composition per 481g: Beef heart........................................................454.0g Proteose peptone...............................................20.0g NaCl....................................................................5.0g Glucose ...............................................................2.0g
Source: Cooked meat medium is available in dehydrated form from BD Diagnostic Systems.
Diluent: Composition per liter: Pancreatic digest of casein................................10.0g Glucose ...............................................................2.0g Soluble starch......................................................1.0g Sodium thioglycolate ..........................................1.0g Neutral Red (1% aqueous).............................. 5.0mL
Preparation of Diluent: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat until dissolved.
Preparation of Medium: Add 1.0g of dehydrated cooked meat medium and 15.0mL diluent to 20 × 150mm test tubes. Let meat particles rehydrate. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of anaerobic bateria.
Cooked Meat Medium, Modified
Composition per liter:
Composition per liter:
Heart tissue granules.........................................98.0g Peptic digest of animal tissue............................20.0g NaCl ....................................................................5.0g Glucose ...............................................................5.0g Yeast extract........................................................5.0g Hemin...............................................................5.0mg Vitamin K.........................................................1.0mg pH 7.2 ± 0.2 at 25°C
Solution A: Composition per liter:
Cooked meat medium .......................................66.0g Solution A.......................................................... 1.0L pH 6.8 ± 0.2 at 25°C
Pancreatic digest of casein................................10.0g Glucose ...............................................................2.0g Soluble starch......................................................1.0g
162
Cooked Meat Medium with Peptone and Yeast Extract
Sodium thioglycolate ..........................................1.0g Neutral Red (1% aqueous) .............................. 5.0mL
Preparation of Solution A: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat until dissolved.
Preparation of Medium: Add 1.0g of cooked meat medium to each of 66 test tubes. Add 15.0mL of solution A to each test tube. Allow meat particles to rehydrate. Autoclave for 15 min at 15 psi pressure–121°C. Use: For the cultivation of a variety of anaerobic mi-
Preparation of Medium: Add cornmeal polenta to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Continue boiling for 30 min. Filter through Whatman #1 filter paper. Add agar to filtrate. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 10 min at 15 psi pressure– 121°C. Pour into sterile Petri dishes or leave in tubes. Use: For the cultivation and maintenance of many filamentous fungi.
Cornmeal Agar
croorganisms.
Cooked Meat Medium with Peptone and Yeast Extract Composition per liter: Heart muscle ...................................................454.0g Peptone..............................................................40.0g Beef extract .......................................................10.0g NaCl ....................................................................5.0g Yeast extract........................................................5.0g Glucose ...............................................................2.0g pH 7.2 ± 0.2 at 25°C
Preparation of Medium: Finely chop beef heart. Add approximately 1.5g of heart particles to test tubes. Add remaining components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes in 10.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C. Slowly cool tubes to prevent expulsion of meat particles.
Use: For the cultivation and maintenance of Peptostreptococcus magnus.
Cornmeal Agar (ATCC Medium 307) Composition per liter: Cornmeal...........................................................50.0g Agar ....................................................................7.5g
Preparation of Medium: Add cornmeal to distilled/deionized water and bring volume to 800.0mL. Leave overnight in refrigerator. Heat to 60°C for 1h. Bring volume to 1.0L with distilled/deionized water. Add agar. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation and maintenance of numerous fungi.
Cornmeal Agar (CMA)
Composition per liter: Agar ..................................................................15.0g Cornmeal, solids from infusion ..........................2.0g pH 5.6–6.0 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems and Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat until boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure– 121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of fungi.
Cornmeal Agar with Strep100 and Tet100 (ATCC Medium 2285) Composition per liter: Agar ..................................................................15.0g Cornmeal, solids from infusion ..........................2.0g Antibiotic solution ........................................ 10.0mL pH 5.6–6.0 at 25°C
Source: This medium without antibiotics is available as a premixed powder from BD Diagnostic Systems and Oxoid Unipath.
Preparation of Medium: Add components except antibiotic solution to 990.0mL distilled/deionized water. Mix thoroughly. Gently heat until boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45-50°C. Aseptically add 10.0mL sterile antibiotic solution. Mix thoroughly. Pour into sterile Petri dishes or leave in tubes. Antibiotic Solution: Composition per 10.0mL: Tetracycline.........................................................0.1g Streptomycin sulfate ...........................................0.1g
Composition per liter:
Preparation of Antibiotic Solution: Add com-
Agar ..................................................................20.0g Cornmeal polenta..............................................15.0g pH 7.0 ± 0.2 at 25°C
Use: For the cultivation and maintenance of fungi.
ponents to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Creatinine Medium
Cornmeal Yeast Glucose Agar (CMYG) Composition per liter: Agar ..................................................................15.0g Cornmeal, solids from infusion ..........................2.0g Glucose ...............................................................2.0g Yeast extract........................................................1.0g pH 5.6–6.0 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat until boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
163
Creatinine Agar Composition per liter: Agar ..................................................................15.0g Na2HPO4·12H2O ................................................9.0g NaCl....................................................................5.0g KH2PO4 ..............................................................1.5g Creatinine............................................................1.0g Meat extract ........................................................1.0g Yeast extract........................................................1.0g MgSO4·7H2O......................................................0.2g MnCl2·4H2O ..................................................20.0mg CaCl2 ...............................................................1.2mg Glucose solution ......................................... 100.0mL
Use: For the cultivation of numerous filamentous fun-
Glucose Solution: Composition per 100.0mL:
gi.
Glucose ...............................................................5.0g
CREA (Creatine Agar) Composition per liter: Sucrose..............................................................30.0g Agar ..................................................................15.0g Creatin·H2O ........................................................3.0g K3P04·7H2O ........................................................1.6g Bromcresol Purple .........................................50.0mg Minerals solution .......................................... 10.0mL Trace minerals solution................................... 1.0mL
Minerals Solution: Composition per 100.0mL: KCl......................................................................5.0g MgSO4·7H2O ......................................................5.0g FeSO4·7H2O........................................................0.1g
Preparation of Minerals Solution: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly.
Preparation of Glucose Solution: Add glucose to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize. Warm to 50°C. Preparation of Medium: Add components, except glucose solution, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Aseptically add 100.0mL of sterile glucose solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use:
For the cultivation and maintenance of Pseudomonas species and other bacteria that can utilize creatinine.
Creatinine Medium Composition per liter:
Preparation of Trace Minerals Solution: Add
Creatinine............................................................5.0g Agar ....................................................................2.0g Fumaric acid .......................................................2.0g K2HPO4...............................................................2.0g Yeast extract........................................................1.0g Salt solution .................................................. 10.0mL pH 6.8 ± 0.2 at 25°C
components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly.
Salt Solution: Composition per liter:
Preparation of Medium: Add components to
MgSO4 ..............................................................12.2g FeSO4·7H2O........................................................2.8g MnSO4·H2O ........................................................1.7g CaCl2·2H2O ......................................................0.76g NaCl....................................................................0.6g Na2MoO4·2H2O ..................................................0.1g ZnSO4·7H2O .....................................................0.06g HCl (0.1N solution) ........................................... 1.0L
Trace Minerals Solution: Composition per 100.0mL: ZnS04·7H2O ........................................................1.0g CuSO4·5H2O .......................................................0.5g
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of Penicillium species.
164
CreDm1 Medium
Preparation of Salt Solution: Dissolve salts in 1.0L of 0.1N HCl solution. Mix thoroughly.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 6.8 with NaOH or KOH. Gently heat until boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation and maintenance of Pseudomonas species.
CreDm1 Medium Composition per 1002.0mL: Solution A ................................................... 980.0mL Solution D (Vitamin solution)....................... 10.0mL Solution E ..................................................... 10.0mL Solution B (Trace elements solution SL-10) .. 1.0mL Solution C (Selentite-tungstate solution)........ 1.0mL pH 6.7–6.9 at 25°C
Solution A: Composition per 980.0mL: KH2PO4 ...............................................................1.4g NH4Cl .................................................................0.5g MgCl2·6H2O .......................................................0.2g CaCl2·2H2O.......................................................0.15g Yeast extract...................................................50.0mg
Preparation of Solution A: Add components to distilled/deionized water and bring volume to 980.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C.
Solution B (Trace Elements Solution SL-10): Composition per liter: FeCl2·4H2O .........................................................1.5g CoCl2·6H2O .................................................190.0mg MnCl2·4H2O ................................................100.0mg ZnCl2 ..............................................................70.0mg Na2MoO4·2H2O .............................................36.0mg NiCl2·6H2O ....................................................24.0mg H3BO3 ..............................................................6.0mg CuCl2·2H2O .....................................................2.0mg HCl (25% solution)....................................... 10.0mL
Preparation of Solution B (Trace Elements Solution SL-10): Add FeCl2·4H2O to 10.0mL of
HCl solution. Mix thoroughly. Add distilled/deionized water and bring volume to 1.0L. Add remaining components. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C.
Solution C (Selenite-Tungstate Solution): Composition per liter: NaOH ..................................................................0.5g Na2WO4·2H2O.................................................4.0mg Na2SeO3·5H2O.................................................3.0mg
Preparation of Solution C (Selenite-Tungstate Solution): Add components to distilled/ deionized water and bring volume to 1.0L. Mix thoroughly. Autoclave for 15 min at 15 psi pressure– 121°C.
Solution D (Vitamin Solution): Composition per liter: Pyridoxine·HCl ..............................................10.0mg Calcium DL-pantothenate.................................5.0mg Lipoic acid .......................................................5.0mg Nicotinic acid...................................................5.0mg p-Aminobenzoic acid.......................................5.0mg Riboflavin ........................................................5.0mg Thiamine·HCl ..................................................5.0mg Biotin ...............................................................2.0mg Folic acid .........................................................2.0mg Vitamin B12 ......................................................0.1mg
Preparation of Solution D (Vitamin Solution): Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
Solution E: Composition per 10.0mL: Disodium-DL-malate ...........................................1.6g
Preparation of Solution E: Add disodium-DLmalate to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Preparation of Medium: Aseptically combine 980.0mL of sterile solution A with 1.0mL of sterile solution B, 1.0mL of sterile solution C, 10.0mL of sterile solution D, and 10.0mL of sterile solution E, in that order. Mix thoroughly. Adjust pH to 6.7–6.9. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation of Campylobacter species.
Crystal Violet Agar Composition per liter: Agar ..................................................................15.0g Lactose..............................................................10.0g Proteose peptone.................................................5.0g Beef extract.........................................................3.0g Crystal Violet ...................................................3.3mg pH 6.8 ± 0.1 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat until boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure– 121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the differentiation of pathogenic staphylococci from non-pathogenic staphylococci. Hemolytic and coagulating strains of Staphylococcus aureus ap-
CT Agar pear as purple or yellow colonies. Nonhemolytic and noncoagulating strains of Staphylococcus species appear as white colonies.
Crystal Violet Azide Esculin Agar Composition per liter: Agar ..................................................................15.0g Glucose ...............................................................5.0g NaCl ....................................................................5.0g Proteose peptone .................................................5.0g Pancreatic digest of casein..................................5.0g Meat extract ........................................................3.0g Esculin ................................................................1.0g NaN3 ...................................................................1.0g Crystal Violet ......................................................0.1g Bovine blood, citrated................................. 100.0mL pH 7.5 ± 0.2 at 25°C
Caution: Sodium azide is toxic. Azides also react with metals and disposal must be highly diluted.
Preparation of Medium: Add components, except citrated bovine blood, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile, citrated bovine blood. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation of Erysipelothrix rhusiopathiae.
Crystal Violet Esculin Agar Composition per liter: Agar ..................................................................15.0g Glucose ...............................................................5.0g NaCl ....................................................................5.0g Proteose peptone .................................................5.0g Pancreatic digest of casein..................................5.0g Meat extract ........................................................3.0g Esculin ................................................................1.0g Crystal Violet ...................................................2.0mg Blood, citrated............................................. 100.0mL pH 7.5 ± 0.2 at 25°C
Preparation of Medium: Add components, except citrated blood, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add citrated blood. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
165
CT Agar (Caprylate Thallous Agar) Composition per liter: Solution A................................................... 500.0mL Solution B ................................................... 500.0mL pH 7.2 ± 0.2 at 25°C
Solution A: Composition per 500.0mL: K2HPO4.............................................................2.61g KH2PO4.............................................................0.68g Thallous sulfate.................................................0.25g MgSO4·7H2O ....................................................0.12g CaCl2·2H2O ....................................................0.016g Trace elements solution ................................ 10.0mL Yeast extract.................................................... 2.0mL Caprylic acid................................................... 1.1mL
Preparation of Solution A: Add components to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Adjust pH to 7.2 with NaOH. Autoclave for 20 min at 10 psi pressure– 115°C. Trace Elements Solution: Composition per liter: H3PO4 ...............................................................1.96g FeSO4·7H2O....................................................0.056g ZnSO4·4H2O ...................................................0.029g CuSO4·5H2O ...................................................0.025g MnSO4·4H2O ..................................................0.022g H3BO3 ..............................................................6.2mg Co(NO3)2·6H2O ...............................................3.0mg
Preparation of Trace Elements Solution: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Store at 4°C.
Solution B: Composition per liter: Agar ..................................................................15.0g NaCl....................................................................7.0g (NH4)2SO4 ..........................................................1.0g
Preparation of Solution B: Add components to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Gently heat and bring to boiling. Adjust pH to 7.2. Autoclave for 20 min at 10 psi pressure–115°C.
Preparation of Medium: Aseptically combine 500.0mL of sterile solution A and 500.0mL of sterile solution B. Mix thoroughly. Pour into sterile Petri dishes in 25.0–30.0mL volumes.
Use: For the cultivation of Erysipelothrix rhusio-
Use: For the isolation and cultivation of the Serratia
pathiae.
species.
166
CTA Agar
CTA Agar (Cystine Trypticase Agar) Composition per liter: Pancreatic digest of casein................................20.0g Agar ..................................................................14.0g NaCl ....................................................................5.0g L-Cystine .............................................................0.5g Na2SO3 ................................................................0.5g Phenol Red......................................................0.017g pH 7.3 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat until boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–118°C. Pour into sterile Petri dishes or leave in tubes. Two drops of sterile rabbit serum added per tube prior to solidification enhance the recovery of Corynebacterium diphtheriae.
Use: For the cultivation and maintenance of a variety of fastidious microorganisms, including Corynebacterium diphtheriae. For carbohydrate fermentation tests in the differentiation of Neisseria species.
CTA Medium (Cystine Trypticase Agar Medium) (Cystine Tryptic Agar) Composition per liter: Pancreatic digest of casein................................20.0g NaCl ....................................................................5.0g Carbohydrate.......................................................5.0g Agar ....................................................................2.5g L-Cystine .............................................................0.5g Na2SO3 ................................................................0.5g Phenol Red......................................................0.017g pH 7.3 ± 0.2 at 25°C
Source: The medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.3. Gently heat until boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–118°C. Cool tubes in an upright position. Store at room temperature.
Use: For the cultivation and maintenance of a variety of fastidious microorganisms. For the detection of bacterial motility. Used, with added specific carbohydrate, for fermentation reactions of fastidious microorganisms, especially Neisseria species, pneumococci, streptococci, and nonspore-forming anaerobes.
CTA Medium with Yeast Extract and Rabbit Serum (Cystine Trypticase Agar Medium with Yeast Extract and Rabbit Serum) Composition per liter: Yeast extract......................................................50.0g Pancreatic digest of casein................................20.0g NaCl....................................................................5.0g Carbohydrate.......................................................5.0g Agar ....................................................................2.5g L-Cystine .............................................................0.5g Na2SO3 ................................................................0.5g Phenol Red......................................................0.017g Rabbit serum............................................... 250.0mL pH 7.3 ± 0.2 at 25ºC
Preparation of Medium: Add components, except rabbit serum, to distilled/deionized water and bring volume to 750.0mL. Mix thoroughly. Adjust pH to 7.3. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure–118°C. Cool to 50°C. Aseptically add sterile rabbit serum. Mix thoroughly. Distribute into sterile tubes. Store at room temperature. Do not refrigerate.
Use: For the cultivation and maintenance of fastidious microorganisms, especially mycoplasmas and related microorganisms.
CTLM Medium Composition per 1100.0mL: Beef liver, infusion from.................................125.0g Tryptose ............................................................25.0g Proteose peptone.................................................2.5g L-Cysteine·HCl .................................................1.75g Maltose .............................................................1.25g NaCl..................................................................1.25g Agar ..................................................................1.15g L-Ascorbic acid .................................................0.25g NaHCO3 ..........................................................0.075g Horse serum, heat inactivated..................... 100.0mL Ringer's salt solution, 10× ............................ 75.0mL pH 6.0 ± 0.2 at 25°C
Ringer's Salt Solution, 10×: Composition per 100.0mL: NaCl....................................................................9.0g KCl....................................................................0.42g CaCl2 .................................................................0.24g
Preparation of Ringer's Salt Solution, 10×: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Preparation of Medium: Add components, except horse serum, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to
CYE Agar 6.0. Gently heat and bring to boiling. Autoclave for 25 min at 15 psi pressure–121°C. Cool to 25°C. Aseptically add 100.0mL of sterile, heat-inactivated horse serum. Mix thoroughly. Aseptically distribute into sterile, screw-capped tubes or flasks.
Use: For the cultivation of Trichomonas vaginalis.
CVA Medium (Cefoperazone Vancomycin Amphotericin Medium) Composition per liter: Agar ..................................................................15.0g Casein peptone..................................................10.0g Meat peptone.....................................................10.0g NaCl ....................................................................5.0g Yeast autolysate...................................................2.0g Glucose ...............................................................1.0g NaHSO3 ..............................................................0.1g Sheep blood, defibrinated ............................. 50.0mL CVA antibiotic solution................................. 10.0mL pH 7.0 ± 0.2 at 25°C
CVA Antibiotic Solution: Composition per 10.0mL: Cefoperazone .................................................20.0mg Vancomycin ...................................................10.0mg Amphotericin B................................................2.0mg
Preparation of CVA Antibiotic Solution: Add
167
Neutral Red solution ....................................... 3.0mL Hemin solution................................................ 1.0mL
Egg Yolk Emulsion: Composition: Chicken egg yolks.................................................. 11 Whole chicken egg ..................................................1
Preparation of Egg Yolk Emulsion: Soak eggs with 1:100 dilution of saturated mercuric chloride solution for 1 min. Crack eggs. Separate yolks from whites for 11 eggs. Mix egg yolks with 1 chicken egg.
Antibiotic Solution: Composition per 10.0mL: Cycloserine .........................................................0.5g Cefoxitin .........................................................0.016g
Preparation of Antibiotic Solution: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Neutral Red Solution: Composition per 10.0mL: Neutral Red.........................................................0.1g Ethanol.......................................................... 10.0mL
Preparation of Neutral Red Solution: Add Neutral Red to 10.0mL of ethanol. Mix thoroughly.
Hemin Solution: Composition per 100.0mL:
components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Hemin .................................................................0.5g NaOH (1N solution)...................................... 10.0mL
Preparation of Medium: Add components, ex-
Preparation of Hemin Solution: Add hemin to 10.0mL of 1N NaOH solution. Mix thoroughly. Bring volume to 100.0mL with distilled/deionized water.
cept CVA antibiotic solution and sheep blood, to distilled/deionized water and bring volume to 940.0mL. Mix thoroughly. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°– 50°C. Aseptically add sterile CVA antibiotic solution and sterile, defibrinated sheep blood. Mix thoroughly. Pour into sterile Petri dishes.
Use: For the isolation and cultivation of Campylobacter species from clinical specimens.
Cycloserine Cefoxitin Egg Yolk Fructose Agar Composition per liter: Proteose peptone No. 2 .....................................40.0g Agar ..................................................................25.0g Fructose...............................................................6.0g Na2HPO4 .............................................................5.0g NaCl ....................................................................2.0g KH2PO4 ...............................................................1.0g MgSO4·7H2O ......................................................0.1g Egg yolk emulsion ...................................... 100.0mL Antibiotic solution ........................................ 10.0mL
Preparation of Medium: Add components, except egg yolk emulsion and antibiotic solution, to distilled/deionized water and bring volume to 890.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile egg yolk emulsion and antibiotic solution. Mix thoroughly. Pour into sterile Petri dishes.
Use: For the selective isolation and cultivation of Clostridium difficile from feces.
CYE Agar (Charcoal Yeast Extract Agar) Composition per liter: Agar ..................................................................17.0g Yeast extract......................................................10.0g Charcoal, activated, acid-washed .......................2.0g L-Cysteine·HCl·H2O solution........................ 10.0mL Fe4(P2O7)3 solution ....................................... 10.0mL pH 6.9 ± 0.5 at 50°C
168
CYE Agar, Buffered
L-Cysteine·HCl·H2O
Solution: Composition per 10.0mL: L-Cysteine·HCl·H2O............................................0.4g
Preparation of L-Cysteine·HCl·H2O solution: Add L-cysteine·HCl·H2O to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Fe4(P2O7)3 Solution: Composition per liter:
Preparation of Fe4(P2O7)3 Solution: Add solu-
ble Fe4(P2O7)3 to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. The soluble Fe4(P2O7)3 must be kept dry and in the dark. Do not use if brown or yellow. Prepare solutions freshly. Do not heat over 60°C to dissolve. The mixture dissolves readily in a 50°C water bath.
Preparation of Medium: Add components, ex-
ble Fe4(P2O7)3 to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. The soluble Fe4(P2O7)3 must be kept dry and in the dark. Do not use if brown or yellow. Prepare solutions freshly. Do not heat over 60°C to dissolve. The mixture dissolves readily in a 50°C water bath.
cept L-cysteine·HCl·H2O solution and Fe4(P2O7)3 solution, to distilled/deionized water and bring volume to 980.0mL. Mix thoroughly. Gently heat to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C. Add 10.0mL of sterile L-cysteine·HCl·H2O solution and 10.0mL of sterile Fe4(P2O7)3 solution. Adjust pH to 6.9 at 50°C by adding 4.0–4.5mL of 1.0 N KOH. This is a critical step. Mix thoroughly. Pour in 20.0mL volumes into sterile Petri dishes. Swirl medium while pouring to keep charcoal in suspension.
Preparation of Medium: Add components, ex-
Use: For the cultivation and maintenance of Le-
cept L-cysteine·HCl·H2O solution and Fe4(P2O7)3 solution, to distilled/deionized water and bring volume to 980.0mL. Mix thoroughly. Gently heat to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C. Add 10.0mL of sterile L-cysteine·HCl·H2O solution and 10.0mL of sterile Fe4(P2O7)3 solution. Adjust pH to 6.9 at 50°C by adding 4.0–4.5mL of 1.0N KOH. This is a critical step. Mix thoroughly. Pour in 20.0mL volumes into sterile Petri dishes. Swirl medium while pouring to keep charcoal in suspension.
gionella species.
Fe4(P2O7)3 .........................................................0.25g
Preparation of Fe4(P2O7)3 Solution: Add solu-
Use: For the cultivation and maintenance of Legionella species.
Cystine Heart Agar Composition per liter: Beef heart, solids from infusion......................500.0g Agar ..................................................................15.0g Glucose .............................................................10.0g Proteose peptone...............................................10.0g NaCl....................................................................5.0g L-Cystine .............................................................1.0g Hemoglobin solution .................................. 100.0mL pH 6.8 ± 0.2 at 25°C
CYE Agar, Buffered (Charcoal Yeast Extract Agar, Buffered)
Source: This medium is available as a premixed
Composition per liter:
Hemoglobin Solution: Composition per 100.0mL:
Agar ..................................................................17.0g ACES buffer (N-2-acetamido2-aminoethane sulfonic acid) .....................10.0g Yeast extract......................................................10.0g Charcoal, activated, acid-washed........................2.0g L-Cysteine·HCl·H2O solution........................ 10.0mL Fe4(P2O7)3 solution ....................................... 10.0mL pH 6.9 ± .05 at 50°C L-Cysteine·HCl·H2O
Solution: Composition per 10.0mL: L-Cysteine·HCl·H2O............................................0.4g
Preparation of L-Cysteine·HCl·H2O Solution: Add L-cysteine·HCl·H2O to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Fe4(P2O7)3 Solution: Composition per liter: Fe4(P2O7)3 .........................................................0.25g
powder from BD Diagnostic Systems.
Hemoglobin ........................................................2.0g
Preparation of Hemoglobin Solution: Add hemoglobin to cold distilled/deionized water and bring volume to 100.0mL. Mix thoroughly by shaking for 10–15 min. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 50°–60°C.
Preparation of Medium: Add components, except hemoglobin solution, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50–60°C. Aseptically add 100.0mL of sterile cooled hemoglobin solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation and maintenance of Francisella tularensis and Francisella philomiragia. Without the hemoglobin enrichment, it supports ex-
Czapek Dox Agar, Modified cellent growth of Gram-negative cocci and other pathogenic microorganisms.
Cystine Heart Agar with Rabbit Blood Composition per liter: Beef heart, solids from infusion......................500.0g Agar ..................................................................15.0g Glucose .............................................................10.0g Proteose peptone ...............................................10.0g NaCl ....................................................................5.0g L-Cystine .............................................................1.0g Rabbit blood, defibrinated ............................ 50.0mL pH 6.8 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components, except rabbit blood, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–60°C. Aseptically add 50.0mL of sterile, defibrinated rabbit blood. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation and maintenance of Francisella tularensis and Francisella philomiragia. Without the hemoglobin enrichment, it supports excellent growth of Gram-negative cocci and other pathogenic microorganisms.
Cystine Tellurite Blood Agar Composition per liter: Heart infusion agar...................................... 900.0mL K2TeO3 solution ............................................ 75.0mL Rabbit blood.................................................. 25.0mL L-Cystine ........................................................22.0mg pH 7.4 ± 0.2 at 25°C
Heart Infusion Agar: Composition per 900.0mL:
169
100.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C.
Caution: Potassium tellurite is toxic. Preparation of Medium: Add sterile K2TeO3 solu-
tion, sterile rabbit blood, and sterile, solid L-cystine to sterile, cooled heart infusion agar. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation, differentiation, and cultivation of Corynebacterium diphtheriae. Corynebacterium diphtheriae appears as dark gray to black colonies.
Cystine Tellurite Blood Agar Composition per 120.0mL: Heart infusion agar ..................................... 100.0mL K2TeO3 solution............................................ 15.0mL Sheep blood .................................................... 5.0mL L-Cystine ..........................................................5.0mg pH 7.4 ± 0.2 at 25°C
Heart Infusion Agar: Composition per liter: Beef heart, infusion from................................500.0g Agar ..................................................................20.0g Tryptose ............................................................10.0g Yeast extract........................................................5.0g NaCl....................................................................5.0g
Preparation of Heart Infusion Agar: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
K2TeO3 Solution: Composition per 100.0mL: K2TeO3 ................................................................0.3g
Preparation of K2TeO3 Solution: Add K2TeO3
to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C.
Caution: Potassium tellurite is toxic.
Beef heart, solids from infusion......................500.0g Agar ..................................................................20.0g Tryptose ............................................................10.0g Yeast extract........................................................5.0g NaCl ....................................................................5.0g
lution, sterile, defibrinated sheep blood, and sterile, solid L-cystine to sterile, cooled heart infusion agar. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Preparation of Heart Infusion Agar: Add
Use: For the isolation, differentiation, and cultivation
components to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
K2TeO3 Solution: Composition per 100.0mL: K2TeO3 ................................................................0.3g
Preparation of K2TeO3 Solution: Add K2TeO3
to distilled/deionized water and bring volume to
Preparation of Medium: Add sterile K2TeO3 so-
of Corynebacterium diphtheriae. Corynebacterium diphtheriae appears as dark gray to black colonies.
Czapek Dox Agar, Modified Composition per liter: Sucrose..............................................................30.0g Agar ..................................................................12.0g NaNO3 ................................................................2.0g
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Czapek Dox Broth
Magnesium glycerophosphate ............................0.5g KCl......................................................................0.5g K2SO4................................................................0.35g FeSO4 ................................................................0.01g pH 6.8 ± 0.2 at 25°C
Use: For the cultivation of fungi and bacteria capable
Source: This medium is available as a premixed
Sucrose..............................................................30.0g Agar ..................................................................15.0g NaNO3 ................................................................2.0g K2HPO4...............................................................1.0g KCl......................................................................0.5g MgSO4·7H20 .......................................................0.5g FeSO4·7H2O......................................................0.01g pH 7.3 ± 0.2 at 25°C
powder from Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of numerous fungal species. For chlamydospore production by Candida albicans.
Czapek Dox Broth Composition per liter: Sucrose..............................................................30.0g NaNO3.................................................................3.0g K2HPO4 ...............................................................1.0g MgSO4·7H2O ......................................................0.5g KCl......................................................................0.5g FeSO4·7H2O......................................................0.01g pH 7.3 ± 0.2 at 25°C
Source: This medium is available as a premixed
of utilizing sodium nitrate as the sole source of nitrogen.
Czapek Solution Agar Composition per liter:
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation of Aspergillus, Penicillium, and other fungi. For the cultivation and maintenance of microorganisms that can utilize nitrate as sole nitrogen source.
Czapek Yeast Extract Agar
powder from BD Diagnostic Systems.
Composition per liter:
Preparation of Medium: Add components to
Sucrose..............................................................30.0g Agar ..................................................................15.0g Yeast extract........................................................5.0g NaNO3 ................................................................3.0g K2HPO4...............................................................1.0g MgSO4·7H2O ......................................................0.5g KCl......................................................................0.5g FeSO4·7H2O......................................................0.01g Trace metal solution........................................ 1.0mL pH 7.3 ± 0.2 at 25°C
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation and maintenance of a variety of fungal and bacterial species that can use nitrate as sole nitrogen source.
Czapek Dox Liquid Medium, Modified Composition per liter: Sucrose..............................................................30.0g NaNO3.................................................................2.0g Magnesium glycerophosphate ............................0.5g KCl......................................................................0.5g K2SO4................................................................0.35g FeSO4 ................................................................0.01g pH 6.8 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Trace Metal Solution: Composition per 100.0mL: ZnSO4·7H2O .......................................................1.0g CuSO4·5H2O .......................................................0.5g
Preparation of Trace Metal Solution: Add components to 100.0mL distilled/deionized water. Mix thoroughly.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 6.2. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Decarboxylase Medium, Ornithine Modified
171
Use: For the cultivation and maintenance of a vari-
Use: For the cultivation and differentiation of bacte-
ety of fungal and bacterial species that can use nitrate as sole nitrogen source.
ria based on their ability to decarboxylate the amino acid. Bacteria that decarboxylate arginine, lysine, or ornithine turn the medium turbid purple.
DCLS Agar (Deoxycholate Citrate Lactose Sucrose Agar) Composition per liter: Agar ..................................................................12.0g Sodium citrate·3H2O.........................................10.5g Lactose ................................................................5.0g Na2S2O3 ..............................................................5.0g Sucrose................................................................5.0g Pancreatic digest of casein..................................3.5g Peptic digest of animal tissue..............................3.5g Beef extract .........................................................3.0g Sodium deoxycholate..........................................2.5g Neutral Red .......................................................0.03g pH 7.2 ± 0.1 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems and Oxoid.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Do not overheat. Do not autoclave. Pour into sterile Petri dishes in 20.0mL volumes.
Use: For the selective isolation of Salmonella species, Shigella species, and Vibrio species from fecal specimens.
Decarboxylase Base, Møller Composition per liter:
Decarboxylase Medium Base, Falkow Composition per liter: Amino acid..........................................................5.0g Peptone ...............................................................5.0g Yeast extract........................................................3.0g Glucose ...............................................................1.0g Bromcresol Purple ............................................0.02g Mineral oil .................................................. 200.0mL pH 6.8 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components, except mineral oil, to distilled/deionized water and bring volume to 1.0L. For amino acid, use L-arginine, L-lysine, or L-ornithine. Mix thoroughly. Distribute into screwcapped tubes in 5.0mL volumes. Autoclave medium and mineral oil separately for 15 min at 15 psi pressure– 121°C. After inoculation, overlay medium with 1.0mL of sterile mineral oil per tube.
Use: For the cultivation and differentiation of bacteria based on their ability to decarboxylate the amino acid. Bacteria that decarboxylate arginine, lysine, or ornithine turn the medium turbid purple.
Decarboxylase Medium, Ornithine Modified Composition per liter: L-Ornithine ........................................................10.0g
Amino acid........................................................10.0g Beef extract .........................................................5.0g Peptone................................................................5.0g Glucose ...............................................................0.5g Bromcresol Purple ............................................0.01g Cresol Red........................................................5.0mg Pyridoxal..........................................................5.0mg Mineral oil................................................... 200.0mL pH 6.0 ± 0.2 at 25°C
Meat peptone ......................................................5.0g Yeast extract........................................................3.0g Bromcresol Purple solution ............................ 5.0mL pH 5.5 ± 0.2 at 25°C
Source: This medium is available as a premixed pow-
Add Bromcresol Purple to ethanol. Mix thoroughly. Bring volume to 100.0mL with distilled/deionized water. Mix thoroughly. Filter sterilize.
der from BD Diagnostic Systems.
Preparation of Medium: Add components, except mineral oil, to distilled/deionized water and bring volume to 1.0L. For amino acid, use L-arginine, L-lysine, or L-ornithine. Mix thoroughly. Distribute into screwcapped tubes in 5.0mL volumes. Autoclave medium and mineral oil separately for 15 min at 15 psi pressure– 121°C. After inoculation, overlay medium with 1.0mL of sterile mineral oil per tube.
Bromcresol Purple Solution: Composition per 100.0mL: Bromcresol Purple ..............................................0.2g Ethanol.......................................................... 50.0mL
Preparation of Bromcresol Purple Solution:
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat until dissolved. Adjust pH to 5.5 with HCl or NaOH. Distribute into screw-capped tubes. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation and differentiation of bacteria based on their ability to decarboxylate ornithine.
172
Demi-Fraser Broth
Bacteria that decarboxylate ornithine turn the medium turbid purple.
Demi-Fraser Broth Composition per liter: NaCl ..................................................................20.0g Tryptose ............................................................10.0g Na2HPO4 .............................................................9.6g Beef extract .........................................................5.0g Yeast extract........................................................5.0g LiCl .....................................................................3.0g KH2PO4 .............................................................1.35g Esculin ................................................................1.0g Acriflavin·HCl ...............................................12.5mg Nalidixic acid .................................................10.0mg Ferric ammonium citrate supplement ........... 10.0mL pH 7.2 ± 0.2 at 25°C
Source: This medium is available as a premixed powder and supplement from BD Diagnostic Systems.
Ferric Ammonium Citrate Supplement: Composition per 10.0mL: Ferric ammonium citrate.....................................0.5g
Preparation of Ferric Ammonium Citrate Supplement: Add ferric ammonium citrate to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except ferric ammonium citrate supplement, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Aseptically add 10.0mL of sterile ferric ammonium citrate supplement. Mix thoroughly. Aseptically distribute into sterile tubes or flasks. Use: For the cultivation of Listeria species.
Deoxycholate Agar Composition per liter: Agar ..................................................................16.0g Lactose ..............................................................10.0g NaCl ....................................................................5.0g Pancreatic digest of casein..................................5.0g Peptic digest of animal tissue..............................5.0g K2HPO4 ...............................................................2.0g Ferric citrate........................................................1.0g Sodium citrate .....................................................1.0g Sodium deoxycholate..........................................1.0g Neutral Red .....................................................0.033g pH 7.3 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix
thoroughly. Gently heat and bring to boiling. Do not autoclave. Cool to 45°–50°C. Pour into sterile Petri dishes.
Use: For the selective isolation, cultivation, enumeration, and differentiation of Gram-negative enteric microorganisms from a variety of clinical and nonclinical specimens. Escherichia coli appears as large, flat, rose-red colonies. Enterobacter and Klebsiella species appear as large, mucoid, pale colonies with a pink center. Proteus and Salmonella species appear as large, colorless to tan colonies. Shigella species appear as colorless to pink colonies. Pseudomonas species appear as irregular colorless to brown colonies.
Deoxycholate Agar (Desoxycholate Agar) Composition per liter: Agar ..................................................................15.0g Lactose..............................................................10.0g Peptone .............................................................10.0g NaCl....................................................................5.0g K2HPO4...............................................................2.0g Ferric citrate........................................................1.0g Sodium citrate.....................................................1.0g Sodium deoxycholate..........................................1.0g Neutral Red.......................................................0.03g pH 7.3 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath and BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Do not autoclave. Cool to 50°C. Pour into sterile Petri dishes.
Use: For the selective isolation, cultivation, enumeration, and differentiation of Gram-negative enteric microorganisms from a variety of clinical and nonclinical specimens. Escherichia coli appears as large, flat, rose-red colonies. Enterobacter and Klebsiella species appear as large, mucoid, pale colonies with a pink center. Proteus and Salmonella species appear as large, colorless to tan colonies. Shigella species appear as colorless to pink colonies. Pseudomonas species appear as irregular colorless to brown colonies.
Deoxycholate Citrate Agar Composition per liter: Sodium citrate...................................................50.0g Agar ..................................................................15.0g Lactose..............................................................10.0g Beef extract.........................................................5.0g Peptone ...............................................................5.0g Na2S2O3·5H2O ....................................................5.0g Sodium deoxycholate..........................................2.5g
Deoxycholate Lactose Agar Ferric citrate........................................................1.0g Neutral Red .....................................................0.025g pH 7.3 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Do not autoclave. Cool to 45°–50°C. Pour into sterile Petri dishes. Dry the agar surface before use.
Use: For the selective isolation and cultivation of enteric pathogens, especially Salmonella and Shigella species.
Deoxycholate Citrate Agar Composition per liter: Sodium citrate ...................................................20.0g Agar ..................................................................17.0g Lactose ..............................................................10.0g Meat, solids from infusion ................................10.0g Peptic digest of animal tissue............................10.0g Sodium deoxycholate..........................................5.0g Ferric citrate........................................................1.0g Neutral Red .......................................................0.02g pH 7.3 ± 0.2 at 25°C
173
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Do not autoclave. Cool to 45°–50°C. Pour into sterile Petri dishes. Dry the agar surface before use.
Use: For the selective isolation and cultivation of enteric pathogens, especially Salmonella and Shigella species.
Deoxycholate Citrate Agar, Hynes Composition per liter: Agar ..................................................................12.0g Lactose..............................................................10.0g Sodium citrate.....................................................8.5g Na2S2O3·5H2O ....................................................5.4g Beef extract powder............................................5.0g Peptone ...............................................................5.0g Sodium deoxycholate..........................................5.0g Ferric citrate........................................................1.0g Neutral Red.......................................................0.02g pH 7.3 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath.
Preparation of Medium: Add components to dis-
der from BD Diagnostic Systems.
tilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Do not autoclave. Cool to 45°–50°C. Pour into sterile Petri dishes. Dry the agar surface before use.
Preparation of Medium: Add components to dis-
Use: For the selective isolation, cultivation, and dif-
Source: This medium is available as a premixed pow-
tilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Do not autoclave. Cool to 45°–50°C. Pour into sterile Petri dishes. Dry the agar surface before use.
Use: For the selective isolation and cultivation of enteric pathogens, especially Salmonella and Shigella species.
Deoxycholate Citrate Agar (Desoxycholate Citrate Agar) Composition per liter: Pork infusion...................................................330.0g Sodium citrate ...................................................20.0g Agar ..................................................................13.5g Lactose ..............................................................10.0g Proteose peptone no. 3 ......................................10.0g Sodium deoxycholate..........................................5.0g Ferric ammonium citrate.....................................2.0g Neutral Red .......................................................0.02g pH 7.5 ± 0.2 at 25°C
ferentiation of enteric pathogens, especially Salmonella and Shigella species. Lactose-fermenting bacteria appear as pink colonies that may or may not be surrounded by a zone of precipitated deoxycholate. Nonlactose-fermenting bacteria appear as colorless colonies that are surrounded by a clear orangeyellow zone.
Deoxycholate Lactose Agar Composition per liter: Agar ..................................................................15.0g Lactose..............................................................10.0g NaCl....................................................................5.0g Pancreatic digest of casein..................................5.0g Peptic digest of animal tissue .............................5.0g Sodium citrate.....................................................2.0g Sodium deoxycholate..........................................0.5g Neutral Red.....................................................0.033g pH 7.1 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Source: This medium is available as a premixed pow-
Preparation of Medium: Add components to dis-
der from BD Diagnostic Systems.
tilled/deionized water and bring volume to 1.0L. Mix
174
Dermasel Agar Base
thoroughly. Gently heat and bring to boiling. Do not autoclave. Cool to 45°–50°C. Pour into sterile Petri dishes. Dry the agar surface before use.
Use: For the selective isolation, cultivation, and differentiation of enteric pathogens, especially Salmonella and Shigella species. Lactose-fermenting bacteria appear as pink colonies that may or may not be surrounded by a zone of precipitated deoxycholate. Nonlactose-fermenting bacteria appear as colorless colonies that are surrounded by a clear orange-yellow zone. Also used for the enumeration of coliform bacteria from water, milk, and dairy products.
Dermasel Agar Base
Preparation of Medium: Add components, except gentamycin sulfate and chlortetracycline, to distilled/ deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add gentamycin sulfate and chlortetracycline. Mix thoroughly. Pour into sterile Petri dishes.
Use: For the selective isolation and cultivation of pathogenic fungi from cutaneous sources.
DEV Lactose Peptone MUG Broth Composition per liter:
Glucose .............................................................20.0g Agar ..................................................................14.5g Papaic digest of soybean meal ..........................10.0g Antibiotic inhibitor ....................................... 10.0mL pH 6.8–7.0 at 25°C
Lactose..............................................................10.0g Meat peptone ....................................................10.0g NaCl....................................................................5.0g Tryptophan..........................................................1.0g 4-Methylumbelliferyl-β-D-glucuronide ..............0.1g Bromocresol Purple ..........................................0.01g pH 7.2 ± 0.2 at 37°C
Source: This medium is available as a premixed pow-
Source: This medium is available from Fluka, Sig-
der from Oxoid Unipath.
ma-Aldrich.
Antibiotic Inhibitor: Composition per 10.0mL:
Preparation of Medium: Add components to
Composition per liter:
Cycloheximide ....................................................0.4g Chloramphenicol...............................................0.05g Acetone ......................................................... 10.0mL
Preparation of Antibiotic Inhibitor: Add cycloheximide and chloramphenicol to 10.0mL of acetone. Mix thoroughly.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Do not overheat. Add antibiotic inhibitor. Mix thoroughly. Autoclave for 10 min at 15 psi pressure–121°C. Pour into sterile Petri dishes.
Use: For the isolation and cultivation of dermatophytic fungi isolated from hair, nails, or skin scrapings.
Dermatophyte Test Medium Base Composition per liter:
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into test tubes that contain an inverted Durham tube in 10.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the enrichment and titre determination of coliform bacteria. The presence of E. coli can be demonstrated by fluorescence in the UV and a positive indole test.
Dextrose Agar Composition per liter: Agar ..................................................................15.0g Glucose .............................................................10.0g NaCl....................................................................5.0g Pancreatic digest of casein..................................5.0g Peptic digest of animal tissue .............................5.0g Beef extract.........................................................3.0g pH 6.9 ± 0.2 at 25°C
Agar ..................................................................20.0g Glucose .............................................................10.0g Papaic digest of soybean meal ..........................10.0g Cycloheximide ....................................................0.5g Phenol Red..........................................................0.2g Gentamycin sulfate .............................................0.1g Chlortetracycline.................................................0.1g pH 5.5 ± 0.2 at 25°C
Source: This medium is available as a premixed pow-
Source: This medium is available as a premixed pow-
Use: For use as a base for the preparation of blood
der from BD Diagnostic Systems.
agar.
der from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Dextrose Proteose No. 3 Agar
Dextrose Agar
175
Source: This medium is available as a premixed pow-
Composition per liter:
der from BD Diagnostic Systems and Oxoid Unipath.
Agar ..................................................................15.0g Glucose .............................................................10.0g Tryptose ............................................................10.0g NaCl ....................................................................5.0g Beef extract .........................................................3.0g pH 7.3 ± 0.2 at 25°C
Preparation of Medium: Add components to dis-
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
tilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the isolation and enrichment of fastidious or damaged microorganisms.
Dextrose Broth Composition per liter: Pancreatic digest of casein................................10.0g Glucose ...............................................................5.0g NaCl....................................................................5.0g pH 7.3 ± 0.2 at 25°C
Use: For the cultivation of a wide variety of micro-
Source: This medium is available as a premixed pow-
organisms. For use as a base for the preparation of blood agar and for general laboratory procedures.
Preparation of Medium: Add components to dis-
Dextrose Ascitic Fluid Semisolid Agar Composition per liter: Pancreatic digest of casein................................2.66g NaCl ..................................................................1.33g Agar ....................................................................0.5g Phenol Red.......................................................4.8mg Ascitic fluid................................................... 50.0mL Glucose solution ........................................... 15.0mL pH 7.4 ± 0.2 at 25°C
Glucose Solution: Composition per 15.0mL: Glucose ...............................................................3.0g
Preparation of Glucose Solution: Add glucose to distilled/deionized water and bring volume to 15.0mL. Mix thoroughly. Filter sterilize. Preparation of Medium: Add components, except ascitic fluid and glucose solution, to distilled/deionized water and bring volume to 935.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile ascitic fluid and glucose solution. Mix thoroughly. Aseptically distribute into sterile tubes. Use: For the isolation and cultivation of microorganisms from spinal fluid.
Dextrose Broth Composition per liter: Tryptose ............................................................10.0g Glucose ...............................................................5.0g NaCl ....................................................................5.0g Beef extract .........................................................3.0g pH 7.2 ± 0.2 at 25°C
der from BD Diagnostic Systems. tilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation and differentiation of microorganisms based on their ability to ferment glucose. If desired, a Durham tube may be added to the test tubes to determine gas production.
Dextrose Proteose No. 3 Agar Composition per liter: Proteose peptone no. 3......................................20.0g Agar ..................................................................13.0g NaCl....................................................................5.0g Glucose ...............................................................2.0g Tellurite blood solution................................. 50.0mL pH 7.4 ± 0.2 at 25°C
Tellurite Blood Solution: Composition per 60.0mL: Sheep blood, defibrinated ............................. 50.0mL Chapman tellurite solution............................ 10.0mL
Preparation of Tellurite Blood Solution: Aseptically combine 10.0mL of Chapman tellurite solution with 50.0mL of sterile, defibrinated sheep blood. Mix thoroughly.
Chapman Tellurite Solution: Composition per 100.0mL: K2TeO3 ................................................................1.0g
Preparation of Chapman Tellurite Solution: Add K2TeO3 to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Caution: Potassium tellurite is toxic.
176
Dextrose Starch Agar
Preparation of Medium: Add components, except tellurite blood solution, to distilled/deionized water and bring volume to 940.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 75°–80°C. Aseptically add 50.0mL of sterile tellurite blood solution. Mix thoroughly. Maintain at 75°–80°C for 10–15 min or until the agar becomes chocolatized. Cool slowly to 50°C. Pour into sterile Petri dishes or distribute into sterile tubes.
Source: This medium is available as a premixed powder from Oxoid Unipath.
Preparation of Medium: Add components, ex-
Use: For propagating pure cultures of Neisseria gon-
cept horse blood, to 930.0mL distilled/deionized water in a 2.5L flask. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C. Aseptically add 70.0mL sterile horse blood. Mix thoroughly to ensure adequate aeration of the blood. Pour into sterile Petri dishes or distribute into sterile tubes.
orrhoeae and other fastidious microorganisms.
Use: For antimicrobial testing of a various patho-
Dextrose Starch Agar Composition per liter: Gelatin...............................................................20.0g Proteose peptone ...............................................15.0g Agar ..................................................................10.0g Starch ................................................................10.0g Glucose ...............................................................5.0g NaCl ....................................................................5.0g Na2HPO4 .............................................................3.0g pH 7.3 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of Neisseria gonorrhoeae, Neisseria animalis, and other fastidious microorganisms.
Diagnostic Sensitivity Test Agar (DST AGAR) Composition per liter: Agar ..................................................................12.0g Proteose peptone ...............................................10.0g Veal infusion solids...........................................10.0g NaCl ....................................................................3.0g Glucose ...............................................................2.0g Na2HPO4 .............................................................2.0g Sodium acetate....................................................1.0g Adenine sulfate .................................................0.01g Guanine hydrochloride .....................................0.01g Uracil ................................................................0.01g Xanthine............................................................0.01g Aneurine......................................................0.00002g Horse blood, sterile lysed or defibrinated ..... 70.0mL pH 7.4 ± 0.2 at 25°C
genic microorganisms. DSTA is primarily used for susceptibility tests rather than the primary isolation of organisms from clinical samples. An essential requirement for satisfactory antimicrobial susceptibility media is that the reactive levels of thymidine and thymine must be sufficiently reduced to avoid antagonism of trimethoprim and sulphonamides. DSTA meets this requirement and in the presence of lysed horse blood (or defibrinated horse blood if the plates are stored long enough to allow some lysis of the erythrocytes) the level of thymidine will be further reduced. This is caused by the action of the enzyme thymidine phosphorylase which is released from lysed horse erythrocytes. Thymidine is an essential growth factor for thymidine-dependent organisms and they will not grow in its absence or they will grow poorly in media containing reduced levels.
Diagnostic Sensitivity Test Agar (DST Agar) Composition per liter: Agar ..................................................................12.0g Proteose peptone...............................................10.0g Veal infusion solids...........................................10.0g NaCl....................................................................3.0g Na2HPO4 .............................................................2.0g Glucose ...............................................................2.0g Sodium acetate....................................................1.0g Adenine sulfate .................................................0.01g Guanine·HCl .....................................................0.01g Uracil ................................................................0.01g Xanthine............................................................0.01g Thiamine ........................................................0.02mg Horse blood, defibrinated ............................. 70.0mL pH 7.4 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath.
Preparation of Medium: Add components, except horse blood, to distilled/deionized water and bring volume to 930.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile
Differential Agar Medium A8 for Ureaplasma urealyticum
177
horse blood. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Use: For the cultivation of microorganisms for anti-
Preparation of Medium: Add components, except diethyl phosphonate solution, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C. Aseptically add 100.0mL diethyl phosphate solution. Mix. Pour into sterile Petri dishes or distribute into sterile tubes.
microbial sensitivity testing.
Diamonds Medium, Modified Composition per liter: Pancreatic digest of casein................................20.0g Yeast extract........................................................1.0g L-Cysteine·HCl·H2O............................................0.5g Maltose................................................................0.5g L-Ascorbic acid .................................................0.02g Horse serum, inactivated............................. 100.0mL Antibiotic inhibitor ....................................... 10.0mL pH 6.5 ± 0.2 at 25°C
Antibiotic Inhibitor: Composition per 10.0mL: Streptomycin sulfate .........................................0.15g Amphotericin B................................................0.2mg Penicillin G ................................................100,000U
Preparation of Antibiotic Inhibitor: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except antibiotic inhibitor and horse serum, to distilled/deionized water and bring volume to 890.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C. Aseptically add sterile antibiotic inhibitor and horse serum. Mix thoroughly. Aseptically distribute into sterile tubes in 5.0mL volumes.
Use: For the cultivation of Trichomonas species.
Diethyl Phosphonate Agar Composition per liter: Agar ..................................................................12.0g Tris(hydroxymethyl)methylamine ......................6.0g p-Hydroxybenzoate, Na salt .............................0.75g KCl......................................................................0.2g MgSO4·7H2O ......................................................0.2g NH4Cl .................................................................0.2g Diethyl phosphonate solution ..................... 100.0mL pH 7.4 ± 0.2 at 25°C
Use: For the cultivation and maintenance of Comamonas acidovorans.
Differential Agar Medium A8 for Ureaplasma urealyticum Composition per 103.1mL: Basal agar...................................................... 80.0mL Horse serum, unheated.................................. 20.0mL Fresh yeast extract solution ............................ 1.0mL Urea solution................................................... 1.0mL CVA enrichment ............................................. 0.5mL L-Cysteine·HCl·H2O solution.......................... 0.5mL GHL tripeptide solution.................................. 0.1mL pH 5.5 ± 0.2 at 25°C
Basal Agar: Composition per 80.0mL: Tryptic soy broth.................................................2.4g Noble agar.........................................................1.05g Putrescine·2HCl ................................................0.17g CaCl2·2H2O ....................................................0.015g
Preparation of Basal Agar: Add components to distilled/deionized water and bring volume to 80.0mL. Mix thoroughly. Adjust pH to 5.5 with 2N HCl. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Fresh Yeast Extract Solution: Composition per 100.0mL: Baker’s yeast, live, pressed, starch-free............25.0g
Preparation of Fresh Yeast Extract Solution: Add the live Baker’s yeast to 100.0mL of distilled/ deionized water. Autoclave for 90 min at 15 psi pressure–121°C. Allow to stand. Remove supernatant solution. Adjust pH to 6.6–6.8. Filter sterilize. Urea Solution: Composition per 30.0mL:
Diethyl Phosphonate Solution: Composition per 100.0mL:
Urea.....................................................................3.0g
Diethyl phosphonate .......................................0.015g
tilled/deionized water and bring volume to 30.0mL. Mix thoroughly. Filter sterilize.
Source: Diethyl phosphonate is available from Eastman Organic Chemical Division, Rochester, NY.
Preparation of Diethyl Phosphonate Solution: Add diethyl phosphonate to distilled/deionized water
Preparation of Urea Solution: Add urea to dis-
CVA Enrichment: Composition per liter: Glucose ...........................................................100.0g
178
Dilute Peptone Water
L-Cysteine·HCl·H2O..........................................25.9g L-Glutamine.......................................................10.0g
Dilute Potato Medium (DSMZ Medium 789)
Adenine...............................................................1.0g L-Cystine·2HCl....................................................1.0g Nicotinamide adenine dinucleotide ..................0.25g Cocarboxylase.....................................................0.1g Guanine·HCl .....................................................0.03g Fe(NO3)3 ...........................................................0.02g Vitamin B12 .......................................................0.01g p-Aminobenzoic acid......................................0.013g Thiamine·HCl ..................................................3.0mg
Composition per liter:
Preparation of CVA Enrichment: Add compo-
Preparation of Potato Decoction: Add diced po-
nents to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize. L-Cysteine·HCl·H2O
Solution: Composition per 50.0mL: L-Cysteine·HCl·H2O ...........................................1.0g
Preparation of L-Cysteine·HCl·H2O Solution:
Add L-cysteine·HCl·H2O to distilled/deionized water and bring volume to 50.0mL. Mix thoroughly. Filter sterilize.
GHL Tripeptide Solution: Composition per 10.0mL: GHL tripeptide.................................................0.2mg
Preparation of GHL Tripeptide Solution: Add GHL tripeptide (glycyl-L-histidyl-L-lysine acetate) to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: To 80.0mL of cooled, sterile basal agar, aseptically add 20.0mL of sterile horse serum, 1.0mL of sterile fresh yeast extract solution, 1.0mL of sterile urea solution, 0.5mL of sterile CVA enrichment, 0.5mL of sterile L-cysteine·HCl·H2O solution, and 0.1mL of sterile GHL tripeptide solution. Mix thoroughly. Pour into sterile Petri dishes in 20.0mL volumes.
Use: For the cultivation and maintenance of Ureaplasma urealyticum.
Dilute Peptone Water Composition per liter: NaCl ....................................................................1.0g Peptone................................................................1.0g pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of various heterotrophic bacteria.
Glucose ...............................................................1.0g Na2HPO4 ...........................................................0.12g Ca(NO3)2·4H2O ................................................0.05g Peptone .............................................................0.05g Potato decoction.......................................... 100.0mL pH 7.3 ± 0.2 at 25°C
Potato Decoction: Diced potato......................................................20.0g tatoes to distilled/deionized water and bring volume to 1.0L. Boil for 30 min. Filter to remove solid potatoes. Bring volume to 1.0L with distilled/deionized water.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of various fungi.
Diphasic Blood Agar Base Medium (ATCC Medium 449) Composition per 500.0mL: Beef...................................................................25.0g Agar ..................................................................10.0g Neopeptone .......................................................10.0g NaCl....................................................................2.5g
Preparation of Diphasic Blood Agar Base Medium: Trim beef to remove fat. Add 25.0g of lean beef to 250.0mL of distilled/deionized water. Gently heat and bring to boiling. Boil for 2-3 min. Filter through Whatman #2 filter paper. Add agar, neopeptone, and NaCl to filtrate. Bring volume to 500.0mL with distilled/deionized water. Mix thoroughly. Adjust pH to 7.2–7.4. Gently heat and bring to boiling. Autoclave for 20 min at 15 psi pressure–121°C. Cool to 50°–55°C. Add as required to other diphasic blood agars.
Use: As the base medium for diphasic blood agars.
Diphasic Blood Agar Medium with 10% Blood Composition per 1120.0mL: Blood agar, diphasic base medium ............. 630.0mL Locke’s solution.......................................... 420.0mL Rabbit blood, defibrinated ............................ 70.0mL pH 7.2–7.4 at 25°C
Blood Agar, Diphasic Base Medium: Composition per 750.0mL: Beef...................................................................25.0g Agar ..................................................................10.0g
Diphasic Medium for Amoeba Neopeptone .......................................................10.0g NaCl ....................................................................2.5g
Preparation of Blood Agar, Diphasic Base Medium: Trim beef to remove fat. Add 25.0g of lean beef to 250.0mL of distilled/deionized water. Gently heat and bring to boiling. Boil for 2-3 min. Filter through Whatman #2 filter paper. Add agar, neopeptone, and NaCl to filtrate. Bring volume to 750.0mL with distilled/deionized water. Mix thoroughly. Adjust pH to 7.2–7.4. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C.
Locke's Solution: Composition per liter: NaCl ....................................................................8.0g Glucose ...............................................................2.5g KH2PO4 .............................................................. 0.3g CaCl2 .................................................................. 0.2g KCl......................................................................0.2g
Preparation of Locke's Solution: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C.
Preparation of Medium: Aseptically combine 630.0mL of sterile blood agar, diphasic base medium, with 70.0mL of sterile defibrinated rabbit blood warmed to 50°–55°C. Mix thoroughly. Aseptically distribute 5.0mL volumes into16 × 125mm screw-capped test tubes. Allow to cool in a slanted position. Overlay the agar in each tube with 3.0mL of sterile Locke’s solution. Use: For the cultivation of Leishmania braziliensis, Leishmania enriettii, Leishmania tropica, Trypanosoma conorrhini, Trypanosoma cruzi, and Trypanosoma rangeli.
Diphasic Blood Agar Medium with 30% Blood Composition per 1450.0mL: Blood agar, diphasic base medium ............. 700.0mL Locke’s solution.......................................... 450.0mL Rabbit blood, defibrinated .......................... 300.0mL pH 7.2–7.4 at 25°C
Blood Agar, Diphasic Base Medium: Composition per 750.0mL: Beef...................................................................25.0g Agar ..................................................................10.0g Neopeptone .......................................................10.0g NaCl ....................................................................2.5g
179
Whatman #2 filter paper. Add agar, neopeptone, and NaCl to filtrate. Bring volume to 750.0mL with distilled/deionized water. Mix thoroughly. Adjust pH to 7.2–7.4. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C.
Locke's Solution: Composition per liter: NaCl....................................................................8.0g Glucose ...............................................................2.5g KH2PO4.............................................................. 0.3g CaCl2 .................................................................. 0.2g KCl......................................................................0.2g
Preparation of Locke's Solution: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C.
Preparation of Medium: Aseptically combine 700.0mL of sterile blood agar, diphasic base medium, with 300.0mL of sterile defibrinated rabbit blood warmed to 50°–55°C. Mix thoroughly. Aseptically distribute 5.0mL volumes into 16 × 125mm screw-capped test tubes. Allow to cool in a slanted position. Overlay the agar in each tube with 3.0mL of sterile Locke’s solution. Use: For the cultivation and maintenance of Leishmania spp. and Trypanosoma spp.
Diphasic Medium for Amoeba (Charcoal Agar Slants) Composition per liter: Agar slants ......................................................... 1.0L Buffered saline overlay...................................... 1.0L pH 7.4 ± 0.2 at 25°C
Agar Slants: Composition per liter: Agar ..................................................................10.0g Charcoal, activated ...........................................10.0g Pancreatic digest of casein..................................5.0g KH2PO4...............................................................4.0g Na2HPO4 .............................................................3.0g Asparagine ..........................................................2.0g Sodium citrate.....................................................1.0g Ferric ammonium citrate.....................................0.1g MgSO4·7H2O ......................................................0.1g Cholesterol solution ...................................... 25.0mL Glycerol ........................................................ 10.0mL
Cholesterol Solution: Composition per 25.0mL:
Preparation of Blood Agar, Diphasic Base Medium: Trim beef to remove fat. Add 25.0g of lean beef
Cholesterol........................................................0.25g Acetone ......................................................... 25.0mL
to 250.0mL of distilled/deionized water. Gently heat and bring to boiling. Boil for 2-3 min. Filter through
lesterol to 25.0mL of acetone. Mix thoroughly.
Preparation of Cholesterol Solution: Add cho-
180
Dixon Agar
Preparation of Agar Slants: Add components, except agar, charcoal, and cholesterol solution, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat to dissolve. Do not boil. Add agar, charcoal, and cholesterol solution. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes in 3.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C. Resuspend charcoal. Allow tubes to cool in a slanted position with short butts or no butts. Buffered Saline Overlay: Composition per liter: NaCl ....................................................................5.0g Solution B ................................................... 810.0mL Solution A ................................................... 190.0mL
Solution A: Composition per liter: KH2PO4, anhydrous ..........................................9.07g
Preparation of Solution A: Add KH2PO4 to dis-
tilled/deionized water and bring volume to 1.0L. Mix thoroughly.
Solution B: Composition per liter: Na2HPO4, anhydrous ........................................9.46g
Preparation of Solution B: Add Na2HPO4 to dis-
tilled/deionized water and bring volume to 1.0L. Mix thoroughly.
Preparation of Buffered Saline Overlay: Combine 810.0mL of solution A and 190.0mL of solution B. Add the NaCl. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C. Store at 4°C.
Preparation of Medium: To each agar slant, aseptically add 3.0mL of sterile, buffered saline overlay.
Use: For the cultivation and maintenance of Amoebae species.
Dixon Agar Composition per liter:
harden. If a lower pH (3.5) is desired, cool medium to 55°C and aseptically add 100.0mL of sterile lactic acid. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation and maintenance of Malassezia species.
DNase Agar Composition per liter: Tryptose ............................................................20.0g Agar ..................................................................12.0g NaCl....................................................................5.0g Deoxyribonucleic acid ........................................2.0g pH 7.3 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the differentiation of microorganisms, especially Staphylococcus species and Serratia marcescens, based on their production of deoxyribo-nuclease.
DNase Medium Composition per liter: Agar ..................................................................15.0g Pancreatic digest of casein................................10.0g Peptic digest of animal tissue ...........................10.0g L-Arabinose .......................................................10.0g NaCl....................................................................5.0g Deoxyribonucleic acid ........................................2.0g Methyl Green ....................................................0.09g Phenol Red........................................................0.05g Antibiotic solution ........................................ 10.0mL pH 7.3 ± 0.2 at 25°C
Antibiotic Solution: Composition per 10.0mL:
Malt extract .......................................................30.0g Oxbile................................................................20.0g Agar ..................................................................15.0g Mycological peptone...........................................5.0g Glycerol mono-oleate .......................................2.50g Tween 40....................................................... 10.0mL pH 5.4 ± 0.2 at 25°C
Cephalothin.......................................................0.01g Ampicillin ........................................................5.0mg Colistimethate ..................................................5.0mg Amphotericin B ...............................................2.5mg
Preparation of Medium: Add components to dis-
Preparation of Medium: Add components, except
tilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring until boiling. Distribute into tubes or flasks. Autoclave for 10 min at 15 psi pressure–115°C. Do not overheat or agar will not
antibiotic solution, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add
Preparation of Antibiotic Solution: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
DTC Agar sterile components. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation and cultivation of Serratia marcescens.
DNase Test Agar Composition per liter: Agar ..................................................................15.0g Pancreatic digest of casein................................15.0g NaCl ....................................................................5.0g Papaic digest of soybean meal ............................5.0g Deoxyribonucleic acid ........................................2.0g pH 7.3 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
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Pancreatic digest of casein................................10.0g Peptic digest of animal tissue ...........................10.0g NaCl....................................................................5.0g Deoxyribonucleic acid ........................................2.0g Toluidine Blue ....................................................0.1g pH 7.3 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 13 psi pressure–118°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the differentiation of microorganisms, especially Staphylococcus species and Serratia marcescens, based on their production of deoxyribonuclease.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 13 psi pressure–118°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the differentiation of microorganisms, especially Staphylococcus species and Serratia marcescens, based on their production of deoxyribonuclease.
DNase Test Agar with Methyl Green Composition per liter: Agar ..................................................................15.0g Pancreatic digest of casein................................10.0g Peptic digest of animal tissue............................10.0g NaCl ....................................................................5.0g Deoxyribonucleic acid ........................................2.0g Methyl Green ....................................................0.05g pH 7.3 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 13 psi pressure–118°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the differentiation of microorganisms, especially Staphylococcus species and Serratia marcescens, based on their production of deoxyribonuclease.
DNase Test Agar with Toluidine Blue Composition per liter: Agar ..................................................................15.0g
Dorset Egg Medium Composition per liter: Homogenized whole egg ............................ 950.0mL Glycerol ........................................................ 50.0mL pH 6.8–7.4 at 25°C
Source: This medium is available as a prepared medium from BD Diagnostic Systems.
Homogenized Whole Egg: Composition per liter: Whole eggs ......................................................18–24
Preparation of Homogenized Whole Egg: Use fresh eggs, less than 1 week old. Scrub the shells with soap. Let stand in a soap solution for 30 min. Rinse in running water. Soak eggs in 70% ethanol for 15 min. Break the eggs into a sterile container. Homogenize by shaking. Filter through four layers of sterile cheesecloth into a sterile graduated cylinder. Measure out 1.0L.
Preparation of Medium: Filter sterilize glycerol. Combine glycerol and homogenized whole egg. Mix thoroughly. Distribute into sterile screw-capped tubes. Place tubes in a slanted position. Inspissate at 85°C (moist heat) for 45 min.
Use: For the maintenance of Mycobacterium species.
DTC Agar Composition per liter: Agar ..................................................................20.0g Pancreatic digest of casein................................15.0g NaCl....................................................................5.0g Papaic digest of soybean meal............................5.0g Deoxyribonucleic acid ........................................2.0g Toluidine Blue O.................................................0.1g Cephalothin solution..................................... 10.0mL
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DTM Agar
Cephalothin Solution: Composition per 10.0mL:
Preparation of Locke Solution: Add compo-
Cephalothin.........................................................1.0g
nents to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation of Cephalothin Solution: Add
Preparation of Medium: Aseptically remove the
cephalothin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except cephalothin solution, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile cephalothin solution. Mix thoroughly. Pour into sterile Petri dishes. Use: For the isolation and cultivation of Serratia species. Serratia appear as colonies with red halos.
DTM Agar (Dermatophyte Test Medium Agar) Composition per liter: Agar ..................................................................20.0g Enzymatic digest of soybean meal....................10.0g Glucose .............................................................10.0g Cycloheximide ....................................................0.5g Phenol Red..........................................................0.2g Chlortetracycline.................................................0.1g Gentamicin..........................................................0.1g pH 7.3 ± 0.2 at 25°C
yolks from 5–8 day old hen egg embryos. Add an equal volume of sterile Locke solution containing sterile glass beads. Mix thoroughly to homogenize. Aseptically distribute into sterile tubes. Inspissate tubes in a slanted position at 80°C (moist heat) for 15 min.
Use: For the cultivation of Calymmatobacter granulomatis from clinical specimens.
Duncan-Strong Sporulation Medium, Modified (DS Sporulation Medium, Modified) (Sporulation Medium, Modified) Composition per liter: Proteose peptone...............................................15.0g Na2HPO4·7H2O.................................................10.0g Raffinose.............................................................4.0g Yeast extract........................................................4.0g Sodium thioglycolate ..........................................1.0g pH 7.8 ± 0.2 at 25°C
Preparation of Medium: Add components to dis-
Diagnostic Systems.
tilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Adjust pH to 7.8 with filter-sterilized 0.66M Na2CO3. Pour into sterile Petri dishes or leave in tubes.
Preparation of Medium: Add components to dis-
Use: For the cultivation and induction of sporulation
Source: Available as a prepared medium from BD
tilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
of Clostridium perfringens.
Dunkelberg Carbohydrate Medium, Modified
Use: For the isolation and cultivation of dermato-
Composition per 100.0mL:
phytic fungi.
Proteose peptone no. 3........................................1.5g Carbohydrate.......................................................1.0g Na2HPO4·2H2O...............................................0.207g Phenol Red......................................................0.055g NaH2PO4·H2O.................................................0.038g Horse serum .................................................... 5.0mL pH 7.4 ± 0.2 at 25°C
Dulaney Slants Composition per liter: Egg yolks ...................................................... 50.0mL Locke solution............................................... 50.0mL
Locke Solution: Composition per 100.0mL: NaCl ....................................................................0.9g Glucose .............................................................0.25g KCl..................................................................0.042g CaCl2·2H2O.....................................................0.024g Na2CO3 .............................................................0.02g
Preparation of Medium: Add components, except horse serum, to distilled/deionized water and bring volume to 95.0mL. For carbohydrate, use glucose, maltose, or starch. Mix thoroughly. Filter sterilize. Aseptically add sterile horse serum. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Eagle Medium Use: For the cultivation and differentiation of Gardnerella vaginalis based on its ability to ferment glucose, maltose, or starch.
Dunkelberg Maintenance Medium Composition per liter: Proteose peptone no. 3 ......................................20.0g Soluble starch....................................................10.0g Agar ....................................................................8.0g Glucose ...............................................................2.0g Na2HPO4 .............................................................1.0g NaH2PO4 .............................................................1.0g pH 6.8 ± 0.2 at 25°C
Preparation of Medium: Add starch to approximately 100.0mL of cold distilled/deionized water. Mix thoroughly. Add starch solution to 400.0mL of boiling distilled/deionized water. Add remaining components. Mix thoroughly. Bring volume to 1.0L with distilled/ deionized water. Distribute into screw-capped tubes. Autoclave for 12 min at 8 psi pressure–112°C.
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Sorbitol .............................................................10.0g NaCl....................................................................5.0g Meat extract ........................................................2.0g Na2S2O3 ..............................................................2.0g Na-deoxycholate ...............................................1.12g Yeast extract........................................................1.0g Ammonium ferric citrate ....................................0.5g 4-methylumbelliferyl-β-D-glucuronide ..............0.1g Bromthymol Blue ...........................................0.025g pH 7.4 ± 0.2 at 37°C
Source: This medium is available from Fluka, Sigma-Aldrich.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 50°C. Pour into sterile Petri dishes.
Use: For the isolation and differentiation of enterohaemorrhagic (EHEC) E. coli O157:H7-strains from clinical specimens.
Use: For the cultivation and maintenance of Gardnerella vaginalis.
Eagle Medium Composition per 99.1mL:
Dunkelberg Semisolid Carbohydrate Fermentation Medium Composition per liter: Proteose peptone no. 3 ......................................20.0g Carbohydrate.....................................................10.0g Agar ....................................................................5.0g Bromcresol Purple solution ............................ 1.0mL pH 7.4 ± 0.2 at 25°C
Bromcresol Purple Solution: Composition per 10.0mL: Bromcresol Purple ............................................0.16g Ethanol (95% solution) ................................. 10.0mL
Preparation of Bromcresol Purple Solution: Add Bromcresol Purple to 10.0mL of ethanol. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. For carbohydrate, use glucose, maltose, or starch. Mix thoroughly. Gently heat and bring to boiling. Filter sterilize. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation and differentiation of Gardnerella vaginalis based on its ability to ferment glucose, maltose, or starch.
E. coli O157:H7 MUG Agar Composition per liter: Casein peptone..................................................20.0g Agar ..................................................................13.0g
Eagle MEM in Hanks BSS ........................... 87.0mL Fetal bovine serum........................................ 10.0mL NaHCO3 (7.5% solution)................................ 1.0mL Penicillin-streptomycin solution..................... 1.0mL Amphotericin B solution................................. 0.1mL pH 7.2–7.4 at 25°C
Eagle MEM in Hanks BSS: Composition per liter: NaCl....................................................................8.0g Glucose ...............................................................1.0g KCl......................................................................0.4g CaCl2·2H2O ......................................................0.14g MgSO4·7H2O ......................................................0.1g KH2PO4.............................................................0.06g Na2HPO4 ...........................................................0.05g L-Isoleucine .....................................................0.026g L-Leucine ........................................................0.026g L-Lysine...........................................................0.026g L-Threonine .....................................................0.024g L-Valine .........................................................0.0235g L-Tyrosine .......................................................0.018g L-Arginine .....................................................0.0174g L-Phenylalanine.............................................0.0165g L-Cystine .........................................................0.012g L-Histidine........................................................8.0mg L-Methionine ....................................................7.5mg Phenol Red.......................................................5.0mg L-Tryptophan....................................................4.0mg Inositol .............................................................1.8mg Biotin ...............................................................1.0mg
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Eagle Medium
Folic acid..........................................................1.0mg Calcium pantothenate ......................................1.0mg Choline chloride...............................................1.0mg Nicotinamide....................................................1.0mg Pyridoxal·HCl ..................................................1.0mg Thiamine·HCl ..................................................1.0mg Riboflavin ........................................................0.1mg
Preparation of Eagle MEM in Hanks BSS: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly.
Penicillin-Streptomycin Solution: Composition per 1.0mL: Streptomycin .....................................................0.01g Penicillin ......................................................10,000U
Preparation of Penicillin-Streptomycin Solution: Add components to distilled/deionized water and bring volume to 1.0mL. Mix thoroughly.
KH2PO4.............................................................0.06g Phenol Red........................................................0.02g
Preparation of Hanks Balanced Salt Solution (10X): Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly.
Tissue Culture Amino Acids (50X): Composition per liter: L-Arginine ...........................................................0.1g L-Lysine...........................................................0.058g L-Isoleucine .....................................................0.052g L-Leucine
........................................................0.052g
L-Threonine .....................................................0.048g L-Valine ...........................................................0.046g L-Tyrosine
.......................................................0.036g
L-Phenylalanine...............................................0.032g L-Histidine.......................................................0.031g L-Cystine .........................................................0.024g
Amphotericin B Solution: Composition per 1.0mL:
L-Methionine ...................................................0.015g
Amphotericin B................................................1.0mg
Preparation of Tissue Culture Amino Acids, Minimal Eagle 50X: Add components to distilled/
Preparation of Amphotericin B Solution:
L-Tryptophan.....................................................0.01g
Add amphotericin B to distilled/deionized water and bring volume to 1.0mL. Mix thoroughly.
deionized water and bring volume to 1.0L. Mix thoroughly.
Preparation of Medium: Combine components.
Tissue Culture Vitamins (100X): Composition per liter:
Mix thoroughly. Filter sterilize.
Use: For the cultivation of animal tissue culture cell lines.
Eagle Medium Composition per liter: Hanks balanced salt solution (10X) ............ 100.0mL Calf serum..................................................... 50.0mL NaHCO3 (7.5% solution) .............................. 29.6mL Tissue culture amino acids (50X) ................. 20.0mL Tissue culture vitamins (100X)..................... 10.0mL Glutamine solution........................................ 10.0mL Phenol Red (0.5% solution) ............................ 4.0mL Penicillin solution ........................................... 1.0mL Streptomycin solution ..................................... 0.4mL pH 7.0 ± 0.2 at 25°C
Hanks Balanced Salt Solution (10X): Composition per 100.0mL: NaCl ....................................................................8.0g Glucose ...............................................................1.0g KCl......................................................................0.4g NaHCO3 ............................................................0.35g CaCl2·2H2O.......................................................0.14g MgCl2·6H2O .......................................................0.1g MgSO4·7H2O ......................................................0.1g Na2HPO4 ...........................................................0.06g
Inositol .............................................................2.0mg Calcium pantothenate ......................................1.0mg Choline chloride...............................................1.0mg Folic acid .........................................................1.0mg Nicotinamide....................................................1.0mg Pyridoxal..........................................................1.0mg Thiamine·HCl ..................................................1.0mg Riboflavin ........................................................0.1mg
Preparation of TC Vitamins, Minimal Eagle 100X: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly.
Glutamine Solution: Composition per 100.0mL: L-Glutamine
........................................................2.9g
Preparation of Glutamine Solution: Add glutamine to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Penicillin Solution: Composition per 1.0mL: Penicillin .................................................... 200,000U
Preparation of Penicillin Solution: Add penicillin to distilled/deionized water and bring volume to 1.0mL. Mix thoroughly.
Eagle Medium, Modified
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Streptomycin Solution: Composition per 1.0mL:
Penicillin-Streptomycin Solution: Composition per 1.0mL:
Streptomycin .......................................................0.5g
Preparation of Streptomycin Solution: Add
Streptomycin.....................................................0.01g Penicillin ...................................................... 10,000U
streptomycin to distilled/deionized water and bring volume to 1.0mL. Mix thoroughly.
Preparation of Penicillin-Streptomycin Solution: Add components to distilled/deionized water
Preparation of Medium: Combine components.
and bring volume to 1.0mL. Mix thoroughly.
Mix thoroughly. Adjust pH to 7.0 with 1N NaOH. Filter sterilize.
Amphotericin B Solution: Composition per 1.0mL:
Use: For the cultivation of animal tissue culture cell
Amphotericin B ...............................................1.0mg
lines, especially for use with rhinoviruses.
Preparation of Amphotericin B Solution:
Eagle Medium Composition per 100.1mL: Eagle MEM in Earle BSS ............................. 94.0mL NaHCO3 (7.5% solution) ................................ 3.0mL Fetal bovine serum, inactivated ...................... 2.0mL Penicillin-streptomycin solution ..................... 1.0mL Amphotericin B solution................................. 0.1mL pH 7.2–7.4 at 25°C
Eagle MEM in Earle BSS: Composition per liter: NaCl ....................................................................6.8g Glucose ...............................................................1.0g KCl......................................................................0.4g CaCl2·2H2O.........................................................0.2g MgCl2·6H2O .......................................................0.2g NaH2PO4 ...........................................................0.15g L-Arginine ...........................................................0.1g L-Lysine.............................................................0.06g L-Isoleucine .......................................................0.05g L-Leucine...........................................................0.05g L-Threonine .......................................................0.05g L-Valine .............................................................0.05g L-Tyrosine..........................................................0.04g L-Phenylalanine.................................................0.03g L-Histidine.........................................................0.03g L-Cystine ...........................................................0.02g L-Methionine .....................................................0.02g L-Tryptophan .....................................................0.01g i-Inositol...........................................................2.0mg Calcium pantothenate ......................................1.0mg Choline chloride...............................................1.0mg Folic acid..........................................................1.0mg Nicotinamide....................................................1.0mg Pyridoxal..........................................................1.0mg Thiamine·HCl ..................................................1.0mg Riboflavin ........................................................0.1mg
Add amphotericin B to distilled/deionized water and bring volume to 1.0mL. Mix thoroughly.
Preparation of Medium: Combine components. Mix thoroughly. Filter sterilize.
Use: For the cultivation of animal tissue culture cell lines.
Eagle Medium, Modified Composition per liter: Eagle MEM (10X) ...................................... 100.0mL Fetal bovine serum...................................... 100.0mL Glucose solution ........................................... 20.0mL HEPES (N-2-Hydroxyethyl piperazine-N´-2-ethanesulfonic acid) buffer, 1M, pH 7.2 .................................. 20.0mL Glutamine solution........................................ 10.0mL NaHCO3 (7.5% solution)................................ 7.5mL Gentamicin sulfate solution ............................ 0.2mL pH 7.2 ± 0.2 at 25°C
Eagle MEM (10X): Composition per 100.0mL: Sterile salt solution ....................................... 97.0mL TC amino acids, minimal Eagle 50X.............. 2.0mL TC vitamins, minimal Eagle 100X ................. 1.0mL
Preparation of Eagle MEM (10X): Combine components. Mix thoroughly. Filter sterilize.
Sterile Salt Solution: Composition per 100.0mL: NaCl....................................................................6.8g Glucose ...............................................................1.0g KCl......................................................................0.4g CaCl2 ...................................................................0.2g MgCl2..................................................................0.2g NaH2PO4 ...........................................................0.15g
Preparation of Eagle MEM in Earle BSS:
Preparation of Sterile Salt Solution: Add com-
Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly.
ponents to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
186
Eagle’s Minimal Essential Medium with Earle’s Salts and Nonessential AAs
Tissue Culture Amino Acids, Minimal Eagle 50X: Composition per liter: L-Arginine ...........................................................0.1g L-Lysine.............................................................0.06g L-Isoleucine .......................................................0.05g L-Leucine...........................................................0.05g L-Threonine .......................................................0.05g L-Valine .............................................................0.05g L-Tyrosine..........................................................0.04g L-Phenylalanine.................................................0.03g L-Histidine.........................................................0.03g L-Cystine ...........................................................0.02g L-Methionine .....................................................0.02g L-Tryptophan .....................................................0.01g
Preparation of Tissue Culture Amino Acids, Minimal Eagle 50X: Add components to distilled/
bring volume to 1.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Combine components. Mix thoroughly. Filter sterilize.
Use: For the cultivation of animal tissue culture cell lines, especially for McCoy cells.
Eagle’s Minimal Essential Medium with Earle’s Salts and Nonessential Amino Acids (MEM with Earle’s Salts and Nonessential Amino Acids) Composition per liter:
Gentamicin Solution: Composition per 1.0mL:
NaCl....................................................................6.8g NaHCO3 ..............................................................2.2g Glucose ...............................................................1.0g KCl......................................................................0.4g CaCl2·2H2O ....................................................0.265g MgSO4·7H2O ......................................................0.2g L-Arginine·H2O .................................................0.15g NaH2PO4·H2O...................................................0.14g L-Arginine·HCl................................................0.126g L-Lysine·HCl ..................................................72.5mg L-Tyrosine, disodium salt ...............................52.1mg L-Leucine .......................................................52.0mg L-Threonine ....................................................48.0mg L-Valine ..........................................................46.0mg L-Histidine·HCl·H2O......................................42.0mg D-Phenylalanine .............................................32.0mg L-Cysteine·2HCl...........................................31.29mg L-Methionine ..................................................15.0mg L-Glutamic acid..............................................14.7mg L-Aspartic acid ...............................................13.3mg L-Proline.........................................................11.5mg L-Serine ..........................................................10.5mg L-Tryptophan..................................................10.0mg Phenol Red.....................................................10.0mg L-Alanine..........................................................8.9mg L-Glycine..........................................................7.5mg i-Inositol...........................................................2.0mg D-Calcium pantothenate ...................................1.0mg Choline chloride...............................................1.0mg Folic acid .........................................................1.0mg Nicotinamide....................................................1.0mg Pyridoxal·HCl ..................................................1.0mg Thiamine·HCl ..................................................1.0mg Riboflavin ........................................................0.1mg pH 7.2 ± 0.2 at 25°C
Gentamicin sulfate ............................................0.05g
Preparation of Medium: Add components to
Preparation of Gentamicin Solution: Add
1.0L of distilled/deionized water. Mix thoroughly. Filter sterilize.
deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.2–7.4. Filter sterilize.
TC Vitamins, Minimal Eagle 100X: Composition per liter: Inositol .............................................................2.0mg Calcium pantothenate ......................................1.0mg Choline chloride...............................................1.0mg Folic acid..........................................................1.0mg Nicotinamide....................................................1.0mg Pyridoxal..........................................................1.0mg Thiamine·HCl ..................................................1.0mg Riboflavin ........................................................0.1mg
Preparation of TC Vitamins, Minimal Eagle 100X: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
Glucose Solution: Composition per 100.0mL: Glucose .............................................................27.0g
Preparation of Glucose Solution: Add glucose to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize. Glutamine Solution: Composition per 10.0mL: L-Glutamine.........................................................5.0g
Preparation of Glutamine Solution: Add glutamine to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
gentamicin sulfate to distilled/deionized water and
EC Medium, Modified with Novobiocin Use: For the cultivation of animal cells in tissue cul-
187
ture, for example cells for viral detection and identification by characteristic cytopathic effects.
Mix thoroughly. Distribute into test tubes that contain an inverted Durham tube. Autoclave for 12 min at 15 psi pressure–121°C. Cool broth as quickly as possible.
Earle’s Balanced Salts, Phenol Red-Free
Use: For the cultivation and differentiation of coliform
Composition per liter: NaCl ....................................................................6.8g NaHCO3 ..............................................................2.2g Glucose ...............................................................1.0g KCl......................................................................0.4g CaCl2·2H2O.....................................................0.265g MgSO4·7H2O ......................................................0.2g NaH2PO4·H2O...................................................0.14g pH 7.2 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
Use: For the preparation of tissue culture media where Phenol Red is not desired.
EB Motility Medium Composition per liter: Peptone or gelysate ...........................................10.0g NaCl ....................................................................5.0g Agar ....................................................................4.0g Beef extract .........................................................3.0g pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes in 8.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation and differentiation of bacteria based on motility.
EC Broth (Escherichia coli Broth) (EC Medium) Composition per liter: Pancreatic digest of casein................................20.0g Lactose ................................................................5.0g NaCl ....................................................................5.0g K2HPO4 ...............................................................4.0g Bile salts mixture ................................................1.5g KH2PO4 ...............................................................1.5g pH 6.9 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L.
bacteria at 37°C and of Escherichia coli at 45.5°C.
EC Broth with MUG Composition per liter: Pancreatic digest of casein................................20.0g Lactose................................................................5.0g NaCl....................................................................5.0g K2HPO4...............................................................4.0g Bile salts mixture ................................................1.5g KH2PO4...............................................................1.5g 4-Methylumbeliferyl-βD-glucuronide (MUG).................................0.05g pH 6.9 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into test tubes that contain an inverted Durham tube in 10.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the detection of Escherichia coli by a fluorogenic procedure.
EC Medium, Modified with Novobiocin Composition per liter: Tryptone............................................................20.0g NaCl....................................................................5.0g Lactose................................................................5.0g K2HPO4...............................................................4.0g KH2PO4...............................................................1.5g Bile salts............................................................1.12g Novobiocin supplement ................................ 10.0mL pH 6.9 ± 0.2 at 25°C
Source: This medium is available as a premixed powder and supplement from BD Diagnostic Systems.
Novobiocin Supplement: Composition per 10.0mL: Sodium novobiocin........................................20.0mg
Preparation of Novobiocin Supplement: Add sodium novobiocin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except novobiocin supplement, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly.
188
ECD MUG Agar
Autoclave for 15 min at 15 psi pressure–121°C. Aseptically add 10.0mL of sterile novobiocin supplement. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Egg Yolk Emulsion: Composition:
Use: For the cultivation of Escherichia coli O157:H7.
Preparation of Egg Yolk Emulsion: Soak eggs
ECD MUG Agar Composition per liter: Casein peptone..................................................20.0g Agar ..................................................................15.0g NaCl ....................................................................5.0g Lactose ................................................................5.0g K2HPO4 ..............................................................4.0g Bile salt mixture..................................................1.5g KH2PO4 ..............................................................1.5g Tryptophan ..........................................................1.0g 4-Methylumbelliferyl-β-D-glucuronide ............0.07g pH 7.0 ± 0.2 at 37°C
Source: This medium is available from Fluka, Sigma-Aldrich.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 50°C. Pour into sterile Petri dishes.
Use: For detection of Escherichia coli in a variety of specimens. The bile-salt mixture in this E. coli direct agar extensively inhibits the non-obligatory intestinal accompanying flora. Fluorescence in the UV and a positive indole test demonstrate the presence of E. coli in the colonies.
Egg Yolk Agar Composition per liter: Proteose peptone no. 2 ......................................40.0g Agar ..................................................................25.0g Na2HPO4 .............................................................5.0g Glucose ...............................................................2.0g NaCl ....................................................................2.0g KH2PO4 ...............................................................1.0g MgSO4·7H2O ......................................................0.1g Egg yolk emulsion ...................................... 100.0mL Hemin solution................................................ 1.0mL pH 7.6 ± 0.2 at 25°C
Hemin Solution: Composition per 100.0mL: Hemin..................................................................0.5g NaOH (1N solution)...................................... 20.0mL
Preparation of Hemin Solution: Add hemin to 20.0mL of 1N NaOH solution. Mix thoroughly. Bring volume to 100.0mL with distilled/deionized water.
Chicken egg yolks.................................................. 11 Whole chicken egg ..................................................1 with 1:100 dilution of saturated mercuric chloride solution for 1 min. Crack eggs and separate yolks from whites. Mix egg yolks with 1 chicken egg.
Preparation of Medium: Add components, except egg yolk emulsion, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile egg yolk emulsion. Mix thoroughly. Pour into sterile Petri dishes.
Use: For the isolation, cultivation, and differentiation of Clostridium species and some other anaerobic bacteria.
Egg Yolk Agar, Modified Composition per liter: Agar ..................................................................20.0g Pancreatic digest of casein................................15.0g Vitamin K1 ........................................................10.0g NaCl....................................................................5.0g Papaic digest of soybean meal............................5.0g Yeast extract........................................................5.0g L-Cystine .............................................................0.4g Hemin ..............................................................5.0mg Egg yolk emulsion ...................................... 100.0mL
Source: This medium is available as a prepared medium from BD Diagnostic Systems.
Egg Yolk Emulsion: Composition: Chicken egg yolks.................................................. 11 Whole chicken egg ..................................................1
Preparation of Egg Yolk Emulsion: Soak eggs with 1:100 dilution of saturated mercuric chloride solution for 1 min. Crack eggs and separate yolks from whites. Mix egg yolks with 1 chicken egg.
Preparation of Medium: Add components, except egg yolk emulsion, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile egg yolk emulsion. Mix thoroughly. Pour into sterile Petri dishes.
Use: For the isolation, cultivation, and differentiation of Clostridium species and some other anaerobic bacteria.
Eijkman Lactose Medium
Egg Yolk Emulsion
189
Sterile saline.................................................. 70.0mL Egg yolk........................................................ 30.0mL
anol for 1h. Crack eggs aseptically and separate yolks from whites. Remove egg yolks with a sterile syringe or a wide-mouth pipet. Place 50.0mL of egg yolks into a sterile container. Add 50.0mL sterile 0.85% saline
Source: Sterile egg yolk emulsion is available from
Use: For use in media requiring egg yolk emulsion.
Composition per 100mL:
Fluka, Sigma-Aldrich.
Preparation of Medium: Use fresh eggs, less than 1 week old. Scrub the shells with soap. Let stand in a soap solution for 30 min. Rinse in running water. Soak eggs in 70% ethanol for 15 min. or soak eggs with 1:100 dilution of saturated mercuric chloride solution for 1 min. Crack eggs and separate yolks from whites, placing egg yolks into a sterile container. Use enough egs to produce at least 30.0mL egg yolk. Homogenize by shaking. Add 0.9g NaCl to distilled/ deionized water and bring volume to 100.0mL. Sterilze the saline solution by filtration or by autoclaving for 15 min at 15 psi pressure–121°C. If autoclaving is used, cool to 25°C. Aseptically add 30.0mL homogenized egg yolks to 70.0mL of sterile saline solution. Mix thoroughly.
Use: Sterile stabilized emulsion of egg yolk recommended for use in various culture media.
Egg Yolk Emulsion Composition per 100mL: NaCl ..................................................................0.45g Egg yolk........................................................ 50.0mL
Preparation of Medium: Use fresh eggs, less than 1 week old. Scrub the shells with soap. Let stand in a soap solution for 30 min. Rinse in running water. Soak eggs in 70% ethanol for 15 min. or soak eggs with 1:100 dilution of saturated mercuric chloride solution for 1 min. Crack eggs and separate yolks from whites, placing egg yolks into a sterile container. Use enough egs to produce at least 50.0mL egg yolk. Homogenize by shaking. Add 0.45g NaCl to distilled/ deionized water and bring volume to 50.0mL. Sterilze the saline solution by filtration or by autoclaving for 15 min at 15 psi pressure–121°C. If autoclaving is used, cool to 25°C. Aseptically add 50.0mL homogenized egg yolks to 50.0mL of the sterile NaCl solution. Mix thoroughly.
Use: Sterile stabilized emulsion of egg yolk recommended for use in various culture media.
Egg Yolk Emulsion, 50% Composition per 100.0mL: Chicken egg yolks.........................................variable NaCl (0.85% solution) .................................. 40.0mL
Egg-yolk Tellurite Emulsion 20% Composition per 100mL: NaCl................................................................0.425g K2TeO3 ..............................................................0.21g Egg yolk........................................................ 20.0mL
Preparation of Medium: Use fresh eggs, less than 1 week old. Scrub the shells with soap. Let stand in a soap solution for 30 min. Rinse in running water. Soak eggs in 70% ethanol for 15 min. or soak eggs with 1:100 dilution of saturated mercuric chloride solution for 1 min. Crack eggs and separate yolks from whites, placing egg yolks into a sterile container. Use enough eggs to produce at least 20.0mL egg yolk. Homogenize by shaking. Add 0.45g NaCl and 0.21g K2TeO3 to distilled/deionized water and bring volume to 80.0mL. Sterilze the saline-tellurite solution by filtration or by autoclaving for 15 min at 15 psi pressure–121°C. If autoclaving is used, cool to 25°C. Aseptically add 20.0mL homogenized egg yolks to 80.0mL of the sterile saline-tellurite solution. Mix thoroughly.
Use: For use in various culture media. It may be added directly to nutrient media for the identification of Clostridium, Bacillus, and Staphylococcus species by their lipase activity.
Eijkman Lactose Medium Composition per liter: Pancreatic digest of casein................................15.0g K2HPO4.............................................................10.0g KH2PO4...............................................................4.0g Lactose................................................................3.0g NaCl....................................................................2.5g pH 6.8 ± 0.1 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into test tubes that contain an inverted Durham tube. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation and differentiation of Escherichia coli from other coliform organisms based on their ability to ferment lactose and produce gas.
Eijkman Lactose Medium
Preparation of Egg Yolk Emulsion: Wash fresh
Composition per liter:
eggs wtih stiff brush and drain. Soak eggs in 70% eth-
Tryptose ............................................................15.0g
190
EMB Agar
NaCl ....................................................................5.0g K2HPO4 ...............................................................4.0g Lactose ................................................................3.0g KH2PO4 ...............................................................1.5g pH 6.8 ± 0.1 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into test tubes that contain an inverted Durham tube. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation and differentiation of Escherichia coli from other coliform organisms based on their ability to ferment lactose and produce gas.
EMB Agar (Eosin Methylene Blue Agar) Composition per liter: Agar ..................................................................13.5g Pancreatic digest of casein................................10.0g Lactose ................................................................5.0g Sucrose................................................................5.0g K2HPO4 ...............................................................2.0g Eosin Y ...............................................................0.4g Methylene Blue...............................................0.065g pH 7.2 ± 0.2 at 25°C
Eosin Y ...............................................................0.4g Methylene Blue...............................................0.065g pH 7.3 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes.
Use: For the isolation, cultivation, and differentiation of Gram-negative enteric bacteria based on lactose fermentation. Bacteria that ferment lactose, especially the coliform bacterium Escherichia coli, appear as colonies with a green metallic sheen or blue-black to brown color. Bacteria that do not ferment lactose appear as colorless or transparent, light purple colonies.
EMB Agar, Modified (Eosin Methylene Blue Agar, Modified) Composition per liter: Agar ..................................................................15.0g Lactose..............................................................10.0g Pancreatic digest of gelatin...............................10.0g K2HPO4...............................................................2.0g Eosin Y ...............................................................0.4g Methylene Blue...............................................0.065g pH 6.8 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Source: This medium is available as a premixed
Preparation of Medium: Add components to
Preparation of Medium: Add components to dis-
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes.
tilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 60°C. Shake medium to oxidize methylene blue. Pour into sterile Petri dishes. Swirl flask while pouring plates to distribute precipitate.
Use: For the isolation, cultivation, and differentiation of Gram-negative enteric bacteria based on lactose fermentation. Bacteria that ferment lactose, especially the coliform bacterium Escherichia coli, appear as colonies with a green metallic sheen or blue-black to brown color. Bacteria that do not ferment lactose appear as colorless or transparent, light purple colonies.
EMB Agar Base Composition per liter: Agar ..................................................................15.0g Peptone..............................................................10.0g K2HPO4 ...............................................................2.0g
powder from Oxoid.
Use: For the isolation, cultivation, and differentiation of Gram-negative enteric bacteria based on lactose fermentation. Bacteria that ferment lactose, especially the coliform bacterium Escherichia coli, appear as colonies with a green metallic sheen or blue-black to brown color. Bacteria that do not ferment lactose appear as colorless or transparent, light purple colonies.
Endo Agar Composition per liter: Agar ..................................................................15.0g Lactose..............................................................10.0g Peptic digest of animal tissue ...........................10.0g
Endo Agar, LES K2HPO4 ...............................................................3.5g Na2SO3 ................................................................2.5g Basic Fuchsin......................................................0.5g pH 7.4 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Caution: Basic Fuchsin is a potential carcinogen and care must be taken to avoid inhalation of the powdered dye and contact with the skin.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Pour into sterile Petri dishes. Swirl flask while pouring plates to keep precipitate in suspension. Protect from the light.
Use: For the selective isolation, cultivation, and differentiation of coliform and other enteric microorganisms based on their ability to ferment lactose. Lactosefermenting bacteria appear as dark red colonies with a gold metallic sheen. Lactose-nonfermenting bacteria appear as colorless or translucent colonies.
Endo Agar Composition per liter: Agar ..................................................................10.0g Lactose ..............................................................10.0g Peptic digest of animal tissue............................10.0g K2HPO4 ...............................................................3.5g Na2SO3 ................................................................2.5g Basic Fuchsin solution .................................... 4.0mL pH 7.5 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid.
Basic Fuchsin Solution: Composition per 10.0mL:
191
flask while pouring plates to keep precipitate in suspension. Protect from the light.
Use: For the selective isolation, cultivation, and differentiation of coliform and other enteric microorganisms based on their ability to ferment lactose. Lactosefermenting bacteria appear as dark red colonies with a gold metallic sheen. Lactose-nonfermenting bacteria appear as colorless or translucent colonies.
Endo Agar, LES (Endo Agar, Laurance Experimental Station) (m-Endo Agar, LES) (m-LES, Endo Agar) Composition per liter: Agar ..................................................................14.0g Lactose................................................................9.4g Peptones (pancreatic digest of casein 65% and yeast extract 35%) .............................7.5g NaCl....................................................................3.7g Pancreatic digest of casein..................................3.7g Peptic digest of animal tissue .............................3.7g K2HPO4...............................................................3.3g Na2SO3 ................................................................1.6g Yeast extract........................................................1.2g KH2PO4...............................................................1.0g Basic Fuchsin......................................................0.8g Sodium lauryl sulfate........................................0.05g Ethanol.......................................................... 20.0mL pH 7.2 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Caution: Basic Fuchsin is a potential carcinogen and care must be taken to avoid inhalation of the powdered dye and contact with the skin.
Preparation of Medium: Add ethanol to approx-
Preparation of Basic Fuchsin Solution: Add Basic Fuchsin to 10.0mL of ethanol. Mix thoroughly.
imately 900.0mL of distilled/deionized water. Add remaining components. Bring volume to 1.0L with distilled/deionized water. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile 60mm Petri dishes in 4.0mL volumes. Protect from the light.
Caution: Basic Fuchsin is a potential carcinogen
Use: For the cultivation and enumeration of coliform
and care must be taken to avoid inhalation of the powdered dye and contact with the skin.
bacteria by the membrane filter method.
Basic Fuchsin......................................................1.0g Ethanol (95% solution) ................................. 10.0mL
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Pour into sterile Petri dishes. Swirl
Endo Agar, LES (m-Endo Agar, LES) Composition per liter: Agar ..................................................................10.0g Lactose................................................................9.4g
192
Endo Broth
Tryptose ..............................................................7.5g NaCl ....................................................................3.7g Peptone................................................................3.7g Pancreatic digest of casein..................................3.7g K2HPO4 ...............................................................3.3g Na2SO3 ................................................................1.6g Yeast extract........................................................1.2g KH2PO4 ...............................................................1.0g Sodium deoxycholate..........................................0.1g Sodium lauryl sulfate ........................................0.05g Basic Fuchsin solution .................................... 8.0mL pH 7.2 ± 0.2 at 25°C
Basic Fuchsin Solution: Composition per 10.0mL: Basic Fuchsin......................................................1.0g Ethanol (95% solution) ................................. 10.0mL
Caution: Basic Fuchsin is a potential carcinogen and care must be taken to avoid inhalation of the powdered dye and contact with the skin.
Preparation of Medium: Add ethanol to approximately 900.0mL of distilled/deionized water. Add remaining components. Bring volume to 1.0L with distilled/deionized water. Mix thoroughly. Gently heat and bring to boiling. Rapidly cool broth below 45°C. Do not autoclave. Use 1.8–2.0mL for each filter pad. Protect from the light. Prepare broth freshly.
Use: For the cultivation and enumeration of coliform bacteria by the membrane filter method.
Enriched Nutrient Broth Composition per liter:
Preparation of Basic Fuchsin Solution: Add Basic Fuchsin to 10.0mL of ethanol. Mix thoroughly.
Beef heart, infusion from................................300.0g Tryptose ..............................................................7.5g NaCl....................................................................3.0g Yeast extract........................................................3.0g Peptone ...............................................................2.5g NaCl....................................................................2.5g Beef extract.........................................................0.5g
Preparation of Medium: Add components to
Preparation of Medium: Add components to
Caution: Basic Fuchsin is a potential carcinogen and care must be taken to avoid inhalation of the powdered dye and contact with the skin.
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Pour into sterile Petri dishes. Swirl flask while pouring plates to keep precipitate in suspension. Protect from the light.
Use: For the cultivation and enumeration of coliform bacteria by the membrane filter method.
Endo Broth (m-Endo Broth) Composition per liter: Lactose ..............................................................12.5g Peptone..............................................................10.0g NaCl ....................................................................5.0g Pancreatic digest of casein..................................5.0g Peptic digest of animal tissue..............................5.0g K2HPO4 ...........................................................4.375g Na2SO3 ................................................................2.1g Yeast extract........................................................1.5g KH2PO4 ...........................................................1.375g Basic Fuchsin....................................................1.05g Sodium deoxycholate..........................................0.1g Ethanol (95% solution) ................................. 20.0mL pH 7.2 ± 0.1 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of fastidious bacteria.
Enrichment Broth for Aeromonas hydrophila Composition per liter: NaCl....................................................................5.0g Maltose ...............................................................3.5g Yeast extract........................................................3.0g Bile salts no. 3.....................................................1.0g L-Cysteine·HCl·H2O ...........................................0.3g Bromthymol Blue .............................................0.03g Novobiocin ......................................................5.0mg pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation and enrichment of Aeromonas hydrophila.
Entamoeba Medium (Endamoeba Medium) Composition per liter: Liver infusion..................................................272.0g
Enterococci Broth, Chromocult Rice powder ......................................................14.2g Agar ..................................................................11.0g Proteose peptone .................................................5.5g Sodium glycerophosphate...................................3.0g NaCl ....................................................................2.7g Horse serum .................................................. 50.0mL pH 7.0 ± 0.2 at 25°C
Source: This medium is available as a premixed
193
inositol, salicin, or xylose), 5.0g of carbohydrate per 100.0mL of distilled/deionized water may be used.
Andrade’s Indicator: Composition per 100.0mL: NaOH (1N solution)...................................... 16.0mL Acid Fuchsin.......................................................0.1g
Caution: Acid Fuchsin is a potential carcinogen
powder from BD Diagnostic Systems.
and care must be taken to avoid inhalation of the powdered dye and contact with the skin.
Rice Powder: Composition per 15.0g:
Preparation of Andrade’s Indicator: Add
Rice powder ......................................................15.0g
Preparation of Rice Powder: Sterilize rice powder at 160°C for 60 min. Do not overheat or rice powder will scorch.
Preparation of Medium: Add components, except horse serum and rice powder, to distilled/deionized water and bring volume to 994.0mL. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes in 7.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C. Allow tubes to cool in a slanted position. Aseptically add enough sterile horse serum to each tube to cover about half the slant. Aseptically add 0.1g of sterile rice powder to each tube.
Use: For the cultivation of Entamoeba histolytica.
Enteric Fermentation Base (Fermentation Base for Campylobacter) Composition per liter: Peptic digest of animal tissue............................10.0g NaCl ....................................................................5.0g Beef extract .........................................................3.0g Carbohydrate solution................................. 100.0mL Andrade’s indicator....................................... 10.0mL pH 7.2 ± 0.1 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Carbohydrate Solution: Composition per 100.0mL: Carbohydrate.....................................................10.0g
Preparation of Carbohydrate Solution: Add carbohydrate to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize. Glucose, lactose, mannitol, sucrose, adonitol, arabinose, cellobiose, dulcitol, glycerol, inositol, salicin, xylose, or other carbohydrates may be used. For the preparation of expensive carbohydrate solutions (adonitol, arabinose, cellobiose, dulcitol, glycerol,
components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly.
Preparation of Medium: Add components, except carbohydrate solution, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes that contain an inverted Durham tube in 9.0mL volumes. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 25°C. Aseptically add 1.0mL of sterile carbohydrate solution per tube. Mix thoroughly.
Use: For the cultivation and differentiation of a variety of bacteria based on their ability to ferment different carbohydrates. Bacteria that produce acid from carbohydrate fermentation turn the medium dark pink to red. Bacteria that produce gas have a bubble trapped in the Durham tube.
Enterobacter Medium Composition per 800.0mL: Casein hydrolysate..............................................2.0g K2HPO4...............................................................1.4g K2SO4 .................................................................1.0g Yeast extract........................................................1.0g KH2PO4...............................................................0.6g MgSO4 ................................................................0.5g Glycerol ........................................................ 20.0mL
Preparation of Medium: Add components to distilled/deionized water and bring volume to 800.0mL. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure– 121°C.
Use: For the cultivation and maintenance of Enterobacter species and Klebsiella pneumoniae.
Enterococci Broth, Chromocult (Chromocult Enterococci Broth) Composition per liter: Peptone ...............................................................8.6g NaCl....................................................................6.4g Tween 80.............................................................2.2g
194
Enterococcosel™ Agar
NaN3 ...................................................................0.6g 5-Bromo-4-chloro-3-indolyl-β-D-glucopyranoside (X-GLU) ......................................................0.04 pH 7.5 ± 0.2 at 25°C
terococci). For the cultivation of staphylococci and Listeria monocytogenes.
Source: This medium is available from Merck.
Composition per liter:
Preparation of Medium: Add components to
Pancreatic digest of casein................................17.0g Oxgall ...............................................................10.0g NaCl....................................................................5.0g Yeast extract........................................................5.0g Peptic digest of animal tissue .............................3.0g Esculin ................................................................1.0g Sodium citrate.....................................................1.0g Ferric ammonium citrate.....................................0.5g NaN3 .................................................................0.25g pH 7.1 ± 0.2 at 25°C
distilled/deionized water and bring volume to 1.0L. Mix well. Distribute into tubes. Autoclave for 15 min at 15 psi pressure–121°C. The prepared broth is clear and yellowish.
Use: For the detection of enterococci. The sodiumazide present in this medium largely inhibits the growth of the accompanying, and especially the Gram-negative microbial flora while sparing the enterococci. The substrate X-GLU (5-bromo-4-chloro3-indolyl-β-D-glucopyranoside) is cleaved, stimulated by selected peptones, by the enzyme β-D-glucosidase which is characteristic for enterococci. This results in an intensive blue-green color of the broth. Azide, at the same time, prevents a false positive result by most other β-D-glucosidase positive bacteria. Therefore, the color-change of the broth largely confirms the presence of enterococci and group D-streptococci.
Enterococcosel™ Agar Composition per liter: Pancreatic digest of casein................................17.0g Agar ..................................................................13.5g Oxgall................................................................10.0g NaCl ....................................................................5.0g Yeast extract........................................................5.0g Peptic digest of animal tissue..............................3.0g Esculin ................................................................1.0g Sodium citrate .....................................................1.0g Ferric ammonium citrate.....................................0.5g NaN3 .................................................................0.25g pH 7.1 ± 0.2 at 25°C
Enterococcosel Broth
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Caution: Sodium azide is toxic. Azides also react with metals and disposal must be highly diluted.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring until dissolved. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation and differentiation of group D streptococci (enterococci).
Enterococcus Agar (m-Enterococcus Agar) (Azide Agar) Composition per liter:
Caution: Sodium azide is toxic. Azides also react
Pancreatic digest of casein................................15.0g Agar ..................................................................10.0g Papaic digest of soybean meal............................5.0g Yeast extract........................................................5.0g KH2PO4...............................................................4.0g Glucose ...............................................................2.0g NaN3 ...................................................................0.4g Triphenyltetrazolium chloride ............................0.1g pH 7.2 ± 0.2 at 25°C
with metals and disposal must be highly diluted.
Source: This medium is available as a premixed
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the rapid, selective isolation, cultivation, and enumeration of fecal group D streptococci (en-
powder from BD Diagnostic Systems.
Caution: Sodium azide is toxic. Azides also react with metals and disposal must be highly diluted.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Cool to 45°–50°C. Do not autoclave. Pour into sterile Petri dishes.
Esculin Broth Use: For the direct plating of specimens for the detection and enumeration of fecal streptococci.
Enterococcus faecium Medium Composition per liter: Sucrose..............................................................97.3g Brain heart, solids from infusion ......................37.0g Agar ..................................................................13.3g NaCl ....................................................................9.3g Yeast extract........................................................5.0g MgSO4 ..............................................................0.25g pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of Enterococcus faecium.
Erythritol Agar Composition per liter: Agar ..................................................................15.0g Erythritol.............................................................2.0g K2HPO4 .............................................................1.15g NH4NO3 ..............................................................1.0g KH2PO4 ...........................................................0.625g MgSO4·7H2O ....................................................0.02g
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of Klebsiella pneumoniae.
Erythritol Broth Composition per liter: Erythritol.............................................................2.0g K2HPO4 .............................................................1.15g NH4NO3 ..............................................................1.0g Yeast extract........................................................1.0g KH2PO4 ...........................................................0.625g MgSO4·7H2O ....................................................0.02g
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of Klebsiella pneumoniae.
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Esculin Agar Composition per liter: Agar ..................................................................15.0g Pancreatic digest of casein................................13.0g NaCl....................................................................5.0g Yeast extract........................................................5.0g Heart muscle, solids from infusion.....................2.0g Esculin ................................................................1.0g Ferric citrate........................................................0.5g pH 7.3 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into screw-capped tubes in 3.0mL volumes. Autoclave for 15 min at 15 psi pressure– 121°C. Allow tubes to cool in a slanted position.
Use: For the cultivation and differentiation of bacteria based on their ability to hydrolyze esculin and produce H2S. Bacteria that hydrolyze esculin appear as colonies surrounded by a reddish-brown to dark brown zone. Bacteria that produce H2S appear as black colonies.
Esculin Agar, Modified CDC Composition per liter: Heart muscle, infusion from ...........................375.0g Agar ..................................................................15.0g Thiotone............................................................10.0g NaCl....................................................................5.0g Esculin ................................................................1.0g Ferric citrate........................................................0.5g pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Cool to 55°C. Adjust pH to 7.0. Distribute into tubes or leave in flask. Autoclave for 20 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes. Allow tubes to cool in inclined position to produce slants
Use: For the differentiation of Enterobacter spp.
Esculin Broth Composition per liter: Beef heart, solids from infusion......................500.0g Tryptose ............................................................10.0g NaCl....................................................................5.0g Agar ....................................................................1.0g Esculin ................................................................1.0g pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L.
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Esculin Iron Agar
Mix thoroughly. Gently heat and bring to boiling. Distribute into screw-capped tubes in 7.0mL volumes. Autoclave for 15 min at 15 psi pressure– 121°C.
Colistin Solution: Composition per 10.0mL:
Use: For the cultivation and differentiation of bacte-
to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
ria based on their ability to hydrolyze esculin. Bacteria that hydrolyze esculin turn the medium brownblack to black.
Esculin Iron Agar Composition per liter: Agar ..................................................................15.0g Esculin ................................................................1.0g Ferric ammonium citrate.....................................0.5g pH 7.1 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes.
Use: For the cultivation and identification of enterococci based on their ability to hydrolyze esculin. Used in conjunction with E agar and the membrane filter method.
Esculin Mannitol Agar Composition per liter: Agar ..................................................................13.5g Polypeptone ......................................................10.0g D-Mannitol ........................................................10.0g Pancreatic digest of casein..................................5.0g Yeast extract........................................................5.0g NaCl ....................................................................5.0g Heart peptone......................................................3.0g Cornstarch...........................................................1.0g Esculin ................................................................1.0g Ferric ammonium citrate.....................................0.5g Phenol Red......................................................0.025g Nalidixic acid solution .................................. 10.0mL Colistin solution............................................ 10.0mL pH 7.3 ± 0.2 at 25°C
Nalidixic Acid Solution: Composition per 10.0mL: Nalidixic acid ..................................................0.015g
Preparation of Nalidixic Acid Solution: Add nalidixic acid to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Colistin..............................................................0.01g
Preparation of Colistin Solution: Add colistin
Preparation of Medium: Add components, except nalidixic acid solution and colistin solution, to distilled/deionized water and bring volume to 980.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C. Aseptically add sterile nalidixic acid solution and colistin solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the selective isolation, cultivation, and differentiation of Staphylococcus aureus and group D streptococci based on mannitol fermentation and hydrolysis of esculin. Bacteria that ferment mannitol appear as yellow colonies surrounded by a yellow zone. Bacteria that hydrolyze esculin appear as dark brown to black colonies surrounded by a dark brown to black zone.
ETGPA (Egg Tellurite Glycine Pyruvate Agar) Composition per liter: Agar ..................................................................17.0g Glycine..............................................................12.0g Sodium pyruvate...............................................10.0g Pancreatic digest of casein................................10.0g Beef extract.........................................................5.0g LiCl .....................................................................5.0g Yeast extract........................................................1.0g Egg yolk emulsion ........................................ 50.0mL K2TeO3 solution............................................ 10.0mL pH 7.0 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Egg Yolk Emulsion: Composition: Chicken egg yolks.................................................. 11 Whole chicken egg ..................................................1
Preparation of Egg Yolk Emulsion: Soak egg with 1:100 dilution of saturated mercuric chloride solution for 1 min. Crack eggs and separate yolks from whites. Mix egg yolks with 1 chicken egg.
K2TeO3 Solution: Composition per 100.0mL: K2TeO3 ................................................................1.0g
Ethyl Violet Azide Broth Preparation of K2TeO3 Solution: Add K2TeO3
to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Caution: Potassium tellurite is toxic. Preparation of Medium: Add components to distilled/deionized water and bring volume to 940.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C. Add 10.0mL of sterile 1% tellurite solution and 50.0mL of sterile egg yolk emulsion. If desired, add sulfamethazine to a final concentration of 50.0mg/mL. Mix thoroughly but gently and pour into sterile Petri dishes.
Use: For the selective isolation and enumeration of coagulase-positive staphylococci from skin. For the differentiation and identification of staphylococci on the basis of their ability to clear egg yolk. Addition of sulfamethazine inhibits the growth of Proteus. Grayblack colonies surrounded by a clear zone are diagnostic for Staphylococcus aureus.
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Ethyl Violet Azide Broth (EVA Broth) Composition per liter: Tryptose ............................................................20.0g Glucose ...............................................................5.0g NaCl....................................................................5.0g K2HPO4...............................................................2.7g KH2PO4...............................................................2.7g NaN3 ...................................................................0.4g Ethyl Violet....................................................0.83mg pH 7.0 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Caution: Sodium azide is toxic. Azides also react with metals and disposal must be highly diluted.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes in 10.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the isolation, cultivation, and enumeration
Ethyl Violet Azide Broth (EVA Broth)
of enterococci from water and other specimens. Fecal enterococci turn the medium turbid with a purple sediment on the bottom of the tube.
Composition per liter: Pancreatic digest of casein................................13.5g Yeast extract........................................................6.5g Glucose ...............................................................5.0g NaCl ....................................................................5.0g K2HPO4 ...............................................................2.7g KH2PO4 ...............................................................2.7g NaN3 ...................................................................0.4g Ethyl Violet ....................................................0.83mg pH 7.0 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Caution: Sodium azide is toxic. Azides also react with metals and disposal must be highly diluted.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes in 10.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the isolation, cultivation, and enumeration of enterococci from water and other specimens. Fecal enterococci turn the medium turbid with a purple sediment on the bottom of the tube.
Ethyl Violet Azide Broth (EVA Broth) Composition per liter: Tryptose ............................................................20.0g Glucose ...............................................................5.0g NaCl....................................................................5.0g K2HPO4...............................................................2.7g KH2PO4...............................................................2.7g NaN3 ...................................................................0.3g Ethyl Violet......................................................0.5mg pH 6.8 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes in 10.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C.
Caution: Sodium azide is toxic. Azides also react with metals and disposal must be highly diluted.
Use: For the isolation, cultivation, and enumeration of enterococci from water and other specimens. Fecal enterococci turn the medium turbid with a purple sediment on the bottom of the tube.
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Eubacterium Medium
Eubacterium Medium Composition per liter: Pancreatic digest of casein................................20.0g Agar ..................................................................15.0g Meat extract ......................................................15.0g Glucose ...............................................................5.0g Na2HPO4·12H2O.................................................4.0g L-Cysteine·HCl ...................................................0.5g pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes. Use freshly prepared medium.
Use: For the cultivation of Eubacterium species.
Eubacterium Medium Composition per liter:
Na4P2O7·10H2O ............................................... 0.25g Sheep blood, defibrinated ............................ 50.0mL Hemin solution............................................... 1.0mL Vitamin K1 solution........................................ 0.1mL pH 7.2 ± 0.2 at 25°C
Vitamin K1 Solution: Composition per 100.0mL: Vitamin K1 ......................................................... 1.0g Ethanol......................................................... 99.0mL
Preparation of Vitamin K1 Solution: Add vitamin K1 to 99.0mL of absolute ethanol. Mix thoroughly.
Hemin Solution: Composition per 100.0mL: Hemin ................................................................ 1.0g NaOH (1N solution)..................................... 20.0mL
Preparation of Hemin Solution: Add hemin to 20.0mL of 1N NaOH solution. Mix thoroughly. Bring volume to 100.0mL with distilled/deionized water.
Beef brain powder...........................................33.33g Pancreatic digest of casein................................15.0g Yeast extract......................................................10.0g Glucose ...............................................................5.5g Yeast extract........................................................5.0g NaCl ....................................................................2.5g Sodium thioglycolate ..........................................1.8g L-Cystine .............................................................0.5g pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Add components, ex-
Preparation of Medium: Add components, ex-
anaerobes from clinical and nonclinical specimens.
cept beef brain powder, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling under 97% N2 + 3% H2. Continue boiling for 15–20 min. Adjust pH to 7.0. Cool to 25°C under 97% N2 + 3% H2. Anaerobically distribute into tubes in 9.0mL volumes. Add 0.3g of beef brain powder to each tube. Cap tubes with rubber stoppers. Place tubes in a press. Autoclave for 15 min at 15 psi pressure–121°C with fast exhaust.
Use: For the cultivation of Eubacterium species.
Fastidious Anaerobe Agar (FAA) Composition per liter: Peptone.............................................................23.0g Agar .................................................................12.0g NaCl ...................................................................5.0g Glucose ..............................................................1.0g L-Arginine ..........................................................1.0g Sodium pyruvate ................................................1.0g Soluble starch.....................................................1.0g L-Cysteine·HCl·H2O ..........................................0.5g Sodium succinate ...............................................0.5g NaHCO3 .............................................................0.4g
cept defibrinated sheep blood, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 50.0mL of sterile defibrinated sheep blood. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation of a variety of fastidious
Fastidious Anaerobe Agar, Alternative Selective (FAA Alternative Selective) Composition per liter: Peptone ............................................................ 23.0g Agar ................................................................. 12.0g NaCl................................................................... 5.0g Glucose .............................................................. 1.0g L-Arginine .......................................................... 1.0g Sodium pyruvate................................................ 1.0g Soluble starch..................................................... 1.0g L-Cysteine·HCl·H2O .......................................... 0.5g Sodium succinate ............................................... 0.5g NaHCO3 ............................................................. 0.4g Na4P2O7·10H2O ............................................... 0.25g Sheep blood, defibrinated ............................ 50.0mL Hemin solution............................................... 1.0mL Vitamin K1 solution........................................ 0.1mL pH 7.2 ± 0.2 at 25°C
Vitamin K1 Solution: Composition per 100.0mL: Vitamin K1 ......................................................... 1.0g Ethanol......................................................... 99.0mL
Fastidious Anaerobe Agar, Selective
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Preparation of Vitamin K1 Solution: Add vitamin K1 to 99.0mL of absolute ethanol. Mix thoroughly.
Hemin Solution: Composition per 100.0mL:
Hemin Solution: Composition per 100.0mL:
Hemin ................................................................ 1.0g NaOH (1N solution)..................................... 20.0mL
Hemin.................................................................1.0g NaOH (1N solution)..................................... 20.0mL
Preparation of Hemin Solution: Add hemin to 20.0mL of 1N NaOH solution. Mix thoroughly. Bring volume to 100.0mL with distilled/deionized water.
Preparation of Hemin Solution: Add hemin to 20.0mL of 1N NaOH solution. Mix thoroughly. Bring volume to 100.0mL with distilled/deionized water.
Preparation of Medium: Add components, except defibrinated sheep blood, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 50.0mL of sterile defibrinated sheep blood. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation of a variety of fastidious anaerobes from clinical and nonclinical specimens.
Fastidious Anaerobe Agar, Alternative Selective with Neomycin, Vancomycin, and Josamycin (FAA Alternative Selective Medium with Neomycin, Vancomycin, and Josamycin) Composition per liter: Peptone.............................................................23.0g Agar .................................................................12.0g NaCl ...................................................................5.0g Glucose ..............................................................1.0g L-Arginine ..........................................................1.0g Sodium pyruvate ................................................1.0g Soluble starch.....................................................1.0g L-Cysteine·HCl·H2O ..........................................0.5g Sodium succinate ...............................................0.5g NaHCO3 .............................................................0.4g Na4P2O7·10H2O ...............................................0.25g Neomycin...........................................................0.1g Sheep blood, defibrinated ............................ 50.0mL Vancomycin solution.................................... 10.0mL Josamycin..................................................... 10.0mL Hemin solution............................................... 1.0mL Vitamin K1 ..................................................... 0.1mL pH 7.2 ± 0.2 at 25°C
Vitamin K1 Solution: Composition per 100.0mL: Vitamin K1 .........................................................1.0g Ethanol ......................................................... 99.0mL
Preparation of Vitamin K1 Solution: Add vitamin K1 to 99.0mL of absolute ethanol. Mix thoroughly.
Vancomycin Solution: Composition per 10.0mL: Vancomycin ....................................................5.0mg
Preparation of Vancomycin Solution: Add vancomycin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. Josamycin Solution: Composition per 10.0mL: Josamycin .......................................................3.0mg
Preparation of Josamycin Solution: Add josamycin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except defibrinated sheep blood, vancomycin solution, and josamycin solution, to distilled/deionized water and bring volume to 930.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 50.0mL of sterile defibrinated sheep blood, 10.0mL vancomycin solution, and 10.0mL of josamycin solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the selective cultivation of Fusobacterium species from clinical and nonclinical specimens.
Fastidious Anaerobe Agar, Selective (FAA Selective) Composition per liter: Peptone ............................................................ 23.0g Agar ................................................................. 12.0g NaCl................................................................... 5.0g Glucose .............................................................. 1.0g L-Arginine .......................................................... 1.0g Sodium pyruvate................................................ 1.0g Soluble starch..................................................... 1.0g L-Cysteine·HCl·H2O .......................................... 0.5g Sodium succinate ............................................... 0.5g NaHCO3 ............................................................. 0.4g Na4P2O7·10H2O ............................................... 0.25g Sheep blood, defibrinated ............................ 50.0mL Hemin solution............................................... 1.0mL Vitamin K1 solution........................................ 0.1mL pH 7.2 ± 0.2 at 25°C
200
Fastidious Anaerobe Agar, Selective with Neomycin and Vancomycin
Vitamin K1 Solution: Composition per 100.0mL: Vitamin K1 .........................................................1.0g Ethanol ......................................................... 99.0mL
Preparation of Vitamin K1 Solution: Add vitamin K1 to 99.0mL of absolute ethanol. Mix thoroughly.
Hemin Solution: Composition per 100.0mL: Hemin.................................................................1.0g NaOH (1N solution)..................................... 20.0mL
Preparation of Vitamin K1 Solution: Add vitamin K1 to 99.0mL of absolute ethanol. Mix thoroughly.
Hemin Solution: Composition per 100.0mL: Hemin ................................................................ 1.0g NaOH (1N solution)..................................... 20.0mL
Preparation of Hemin Solution: Add hemin to 20.0mL of 1N NaOH solution. Mix thoroughly. Bring volume to 100.0mL with distilled/deionized water.
Preparation of Hemin Solution: Add hemin to 20.0mL of 1N NaOH solution. Mix thoroughly. Bring volume to 100.0mL with distilled/deionized water.
Vancomycin Solution: Composition per 10.0mL:
Preparation of Medium: Add components, ex-
Preparation of Vancomycin Solution: Add vancomycin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
cept defibrinated sheep blood, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 50.0mL of sterile defibrinated sheep blood. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation of a variety of fastidious anaerobes from clinical and nonclinical specimens.
Fastidious Anaerobe Agar, Selective with Neomycin and Vancomycin (FAA Selective with Neomycin and Vancomycin) Composition per liter: Peptone.............................................................23.0g Agar .................................................................12.0g NaCl ...................................................................5.0g Glucose ..............................................................1.0g L-Arginine ..........................................................1.0g Sodium pyruvate ................................................1.0g Soluble starch.....................................................1.0g L-Cysteine·HCl·H2O ..........................................0.5g Sodium succinate ...............................................0.5g NaHCO3 .............................................................0.4g Na4P2O7·10H2O ...............................................0.25g Neomycin...........................................................0.1g Sheep blood, defibrinated ............................ 50.0mL Vancomycin solution.................................... 10.0mL Hemin solution............................................... 1.0mL Vitamin K1 solution........................................ 0.1mL pH 7.2 ± 0.2 at 25°C
Vitamin K1 Solution: Composition per 100.0mL: Vitamin K1 .........................................................1.0g Ethanol ......................................................... 99.0mL
Vancomycin ....................................................7.5mg
Preparation of Medium: Add components, except defibrinated sheep blood and vancomycin solution, to distilled/deionized water and bring volume to 940.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C. Aseptically add 50.0mL of sterile defibrinated sheep blood and 10.0mL of vancomycin solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the selective cultivation of Fusobacterium species from clinical and nonclinical specimens.
Fay and Barry Medium Composition per liter: Amino acid....................................................... 10.0g Peptone .............................................................. 5.0g Yeast extract....................................................... 3.0g Bromcresol Purple solution ........................... 5.0mL pH 5.5 ± 0.2 at 25°C
Bromcresol Purple Solution: Composition per 100.0mL: Bromcresol Purple ............................................. 0.2g Ethanol......................................................... 50.0mL
Preparation of Bromcresol Purple Solution: Add Bromcresol Purple to 50.0mL of absolute ethanol. Add distilled/deionized water and bring volume to 100.0mL. Mix thoroughly.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. The amino acid may be L-arginine, L-ornithine, or Llysine, depending on which amino acid decarboxylase activity is being measured. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Fermentation Broth Use: For the determination of decarboxylase activities of Aeromonas species.
FDA Agar (ATCC Medium 182) (AATCC Bacteriostasis Agar) (American Association of Textile Chemists and Colorists Bacteriostasis Agar) Composition per liter: Agar .................................................................15.0g Peptic digest of animal tissue...........................10.0g Beef extract ........................................................5.0g NaCl ...................................................................5.0g pH 6.8 ± 0.1 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For testing the antibacterial activities of antiseptics and disinfectants.
FDA Broth (AATCC Bacteriostasis Broth) (American Association of Textile Chemists and Colorists Bacteriostasis Broth) Composition per liter: Peptic digest of animal tissue...........................10.0g Beef extract ........................................................5.0g NaCl ...................................................................5.0g pH 6.8 ± 0.1 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For testing the antibacterial activities of antiseptics and disinfectants.
Fecal Coliform Agar, Modified (m-Fecal Coliform Agar, Modified) (FCIC) Composition per liter: Agar .................................................................15.0g
201
Inositol ............................................................. 10.0g Tryptose ........................................................... 10.0g Proteose peptone no. 3....................................... 5.0g NaCl................................................................... 5.0g Yeast extract....................................................... 3.0g Bile salts no. 3.................................................... 1.5g Aniline Blue....................................................... 0.1g pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Do not autoclave. Cool to 50°C. Adjust pH to 7.4. Pour into sterile Petri dishes in 20.0mL volumes. Allow surface of plates to dry before using. Use: For the isolation, cultivation, and enumeration of Klebsiella species using the membrane filter method.
Fecal Coliform Agar, Modified Composition per liter: Agar ................................................................. 15.0g Lactose............................................................. 12.5g Tryptose ........................................................... 10.0g Proteose peptone no. 3....................................... 5.0g NaCl................................................................... 5.0g Yeast extract....................................................... 3.0g Bile salts no. 3.................................................... 1.5g Aniline Blue....................................................... 0.1g pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Do not autoclave. Cool to 50°C. Adjust pH to 7.4. Pour into sterile Petri dishes in 20.0mL volumes. Allow surface of plates to dry before using. Use: For the isolation, cultivation, and identification of stressed fecal coliform microorganisms based on their ability to ferment lactose. Lactose-fermenting bacteria turn the medium blue.
Fermentation Broth (CHO Medium) Composition per liter: Pancreatic digest of casein............................... 15.0g Yeast extract....................................................... 7.0g NaCl................................................................... 2.5g Agar ................................................................. 0.75g Sodium thioglycolate ......................................... 0.5g L-Cystine .......................................................... 0.25g Ascorbic acid ..................................................... 0.1g Bromthymol Blue ............................................ 0.01g Carbohydrate or starch solution................. 100.0mL pH 7.0 ± 0.1 at 25°C
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Fermentation Medium
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Carbohydrate Solution: Composition per 100.0mL: Carbohydrate......................................................6.0g
Preparation of Carbohydrate Solution: Add
Agar ................................................................. 17.0g Beef extract........................................................ 3.0g Starch ................................................................. 1.5g L-Cysteine solution ...................................... 10.0mL Fe4(P2O7)3 solution ...................................... 10.0mL pH 6.9 ± 0.05 at 25°C
carbohydrate to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
L-Cysteine
Starch Solution: Composition per 100.0mL:
L-Cysteine·HCl·H2O........................................... 0.4g
Starch .................................................................2.5g
cysteine·HCl·H2O to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Starch Solution: Add starch to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except carbohydrate solution, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 100.0mL of sterile carbohydrate solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks. Loosen caps on tubes. Place in an anaerobic chamber under an atmosphere of 85% N2, 10% H2, and 5% CO2. Fasten the caps securely or maintain in an anaerobic chamber.
Use: For the differentiation of anaerobic bacteria based upon carbohydrate fermentation. Bacteria that ferment carbohydrates turn the medium yellow.
Fermentation Medium Composition per liter: Glucose or mannitol.........................................10.0g Pancreatic digest of casein...............................10.0g Agar ...................................................................2.2g Yeast extract.......................................................1.0g Bromcresol Purple ...........................................0.04g pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 10 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For differentiating Staphylococcus and Micrococcus species based upon the fermentation of glucose and mannitol.
F-G Agar (Feeley-Gorman Agar) Composition per liter: Casein, acid hydrolyzed...................................17.5g
Solution: Composition per 10.0mL: Preparation of L-Cysteine Solution: Add
L-
Fe4(P2O7)3 Solution: Composition per 10.0mL: Fe4(P2O7)3 ........................................................ 0.25g
Preparation of Fe4(P2O7)3 Solution: Add Fe4(P2O7)3 to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. Preparation of Medium: Add components, except L-cysteine solution and Fe4(P2O7)3 solution, to distilled/deionized water and bring volume to 980.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C. Aseptically add 10.0mL of L-cysteine solution. Mix thoroughly. Aseptically add 10.0mL of Fe4(P2O7)3 solution. Mix thoroughly. Adjust pH to 6.9. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation and cultivation of Legionella pneumophila.
F-G Agar with Selenium (Feeley-Gorman Agar with Selenium) Composition per liter: Casein, acid hydrolyzed................................... 17.5g Agar ................................................................. 17.0g Beef extract........................................................ 3.0g Starch ................................................................. 1.5g L-Cysteine solution ...................................... 10.0mL Fe4(P2O7)3 solution ...................................... 10.0mL Na2SeO3·5H2O solution............................... 10.0mL pH 6.9 ± 0.05 at 25°C L-Cysteine
Solution: Composition per 10.0mL: L-Cysteine·HCl·H2O........................................... 0.4g
Preparation of L-Cysteine Solution: Add
L-
cysteine·HCl·H2O to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
FGTC Agar
203
Preparation of Medium: Add components, ex-
Fe4(P2O7)3 Solution: Composition per 10.0mL: Fe4(P2O7)3 ........................................................0.25g
Preparation of Fe4(P2O7)3 Solution: Add Fe4(P2O7)3 to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. Na2SeO3·5H2O Solution: Composition per 10.0mL: Na2SeO3·5H2O.................................................0.01g
Preparation of Na2SeO3·5H2O Solution: Add
Na2SeO3·5H2O to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components—except L-cysteine solution, Fe4(P2O7)3 solution, and Na2SeO3·5H2O solution—to distilled/deionized water and bring volume to 970.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 10.0mL of sterile L-cysteine solution. Mix thoroughly. Aseptically add 10.0mL of sterile Fe4(P2O7)3 solution and 10.0mL of sterile Na2SeO3·5H2O solution. Mix thoroughly. Adjust pH to 6.9. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation and cultivation of Legionella pneumophila.
cept L-cysteine solution and Fe4(P2O7)3 solution, to distilled/deionized water and bring volume to 980.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C. Aseptically add 10.0mL of L-cysteine solution. Mix thoroughly. Aseptically add 10.0mL of Fe4(P2O7)3 solution. Mix thoroughly. Adjust pH to 6.9. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation of Legionella pneumophila.
FGTC Agar Composition per liter: Pancreatic digest of casein............................... 15.0g Agar ................................................................. 15.0g Papaic digest of soybean meal........................... 5.0g NaCl................................................................... 5.0g KH2PO4.............................................................. 5.0g Amylose Azure .................................................. 3.0g Galactose............................................................ 1.0g Thallous acetate ................................................. 0.5g MUG (4-Methylumbelliferyl- α-D-galactoside).. 0.1g NaHCO3 solution ......................................... 20.0mL Gentamicin solution....................................... 2.5mL Tween 80...................................................... 0.75mL pH 7.3 ± 0.2 at 25°C
Gentamicin Solution: Composition per 10.0mL: Gentamicin....................................................... 0.01g
F-G Broth (Feeley-Gorman Broth)
Preparation of Gentamicin Solution: Add
Composition per liter: Casein, acid hydrolyzed...................................17.5g Beef extract ........................................................3.0g Starch .................................................................1.5g L-Cysteine solution ...................................... 10.0mL Fe4(P2O7)3 solution ...................................... 10.0mL pH 6.9 ± 0.05 at 25°C
gentamicin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly.
NaHCO3 Solution: Composition per 20.0mL: NaHCO3 ............................................................. 2.0g
Solution: Composition per 10.0mL:
Preparation of NaHCO3 Solution: Add the NaHCO3 to distilled/deionized water and bring volume to 20.0mL. Mix thoroughly. Filter sterilize. Use freshly prepared solution.
L-Cysteine·HCl·H2O...........................................0.4g
Preparation of Medium: Add components, ex-
Preparation of L-Cysteine Solution: Add
cept NaHCO3 solution, to distilled/deionized water and bring volume to 980.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C. Aseptically add sterile NaHCO3 solution. Mix thoroughly. Pour into sterile Petri dishes.
L-Cysteine
L-
cysteine·HCl·H2O to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Fe4(P2O7)3 Solution: Composition per 10.0mL: Fe4(P2O7)3 ........................................................0.25g
Preparation of Fe4(P2O7)3 Solution: Add
Fe4(P2O7)3 to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Use: For the cultivation, differentiation, and enumeration of Enterococcus species based on starch hydrolysis and production of fluorescence. Bacteria that hydrolyze starch, such as Streptococcus bovis, appear as colonies surrounded by a clear zone. Bac-
204
Fildes Enrichment Agar
teria that produce fluorescence, such as Streptococcus bovis and Enterococcus faecium, appear as colonies surrounded by a zone of bright bluish fluorescence when viewed under a long-wave UV lamp. Other bacteria, such as Enterococcus faecalis, Enterococcus avium, or Streptococcus equinus, do not hydrolyze starch or produce fluorescence.
Fildes Enrichment Agar Composition per liter: Agar .................................................................15.0g Peptone...............................................................5.0g Beef extract ........................................................3.0g Fildes enrichment solution........................... 50.0mL
Fildes Enrichment Solution: Composition per 206.0mL: Pepsin.................................................................1.0g NaCl (0.85% solution) ............................... 150.0mL Sheep blood, defibrinated ............................ 50.0mL HCl................................................................. 6.0mL pH 7.0–7.2 at 25°C
Source: Fildes enrichment solution is available from BD Diagnostic Systems.
Preparation of Fildes Enrichment Solution: Combine components. Mix thoroughly. Incubate at 56°C for 4h. Bring pH to 7.0 with 20% NaOH. Adjust pH to 7.2 with HCl. Do not autoclave. Add 0.25 mL of chloroform and store at 4°C. Before use, heat to 56°C to remove chloroform.
Preparation of Medium: Add components, except Fildes enrichment solution, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 56°C. Aseptically add 50.0mL of sterile Fildes enrichment solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation and cultivation of Haemophilus influenzae.
Fish Peptone Agar Composition per liter: Agar ...................................................................5.0g Maltose...............................................................5.0g NaCl ...................................................................5.0g Peptone...............................................................5.0g Pancreatic digest of casein.................................5.0g Yeast extract.......................................................5.0g Trout tissue extract solution......................... 50.0mL pH 7.0 ± 0.2 at 25°C
Trout Tissue Extract Solution: Composition per liter: Fish (brook trout)........................................... 500.0g Pepsin................................................................. 1.0g HCl, concentrated ........................................ 15.0mL
Preparation of Trout Tissue Extract: Add 1.0L of distilled/deionized water to brook trout and blend for 20–30 min. Add 1.0g of pepsin and 15.0mL of concentrated HCl to digest the trout proteins. Incubate for 12 hr at 45°C. Adjust pH to 7.0. Allow solids to settle. Filter sterilize. Do not autoclave. Store at 5°C.
Preparation of Medium: Add components, except trout tissue extract, to distilled/deionized water and bring volume to 950.0L. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 13 psi pressure–118°C. Cool to 45°–50°C. Aseptically add 50.0mL of sterile trout tissue extract. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation and maintenance of Aeromonas salmonicida.
Fish Peptone Broth Composition per liter: Maltose .............................................................. 5.0g NaCl................................................................... 5.0g Peptone .............................................................. 5.0g Pancreatic digest of casein................................. 5.0g Yeast extract....................................................... 5.0g Trout tissue extract solution......................... 50.0mL pH 7.0 ± 0.2 at 25°C
Trout Tissue Extract Solution: Composition per liter: Fish (brook trout)........................................... 500.0g Pepsin................................................................. 1.0g HCl, concentrated ........................................ 15.0mL
Preparation of Trout Tissue Extract: Add 1.0L of distilled/deionized water to brook trout and blend for 20–30 min. Add 1.0g of pepsin and 15.0mL of concentrated HCl to digest the trout proteins. Incubate for 12 hr at 45°C. Adjust pH to 7.0. Allow solids to settle. Filter sterilize. Do not autoclave. Store at 5°C.
Preparation of Medium: Add components, except trout tissue extract, to distilled/deionized water and bring volume to 950.0L. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 10 psi pressure–118°C. Cool to 45°–50°C. Aseptically add 50.0mL of sterile trout tissue extract. Mix thoroughly. Aseptically distribute into sterile tubes or flasks. Use: For the cultivation of Aeromonas salmonicida.
FLN Medium
Five g Agar (5g Agar) Composition per liter: Glycerol ...........................................................50.0g Agar .................................................................15.0g Yeast extract.......................................................5.0g CaCO3 ................................................................1.0g
205
Preparation of Fluorouracil Solution: Add fluorouracil to 50.0mL of distilled/deionized water. Add 1.0mL of 2N NaOH and bring volume to 100.0mL. Gently heat to 56°C for 2h. Adjust pH to 7.4–7.6 with NaOH. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, ex-
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
cept rabbit serum and fluorouracil solution, to distilled/deionized water and bring volume to 930.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Aseptically add 80.0mL of sterile rabbit serum. Mix thoroughly. Aseptically distribute into sterile tubes or flasks. Immediately prior to use, add 0.1mL of fluorouracil solution per 5.0mL of medium.
Use: For the cultivation and maintenance of Der-
Use: For the isolation, cultivation, and maintenance
Preparation of Medium: Add components to
matophilus congolensis and Geodermatophilus obscurus.
Fletcher Medium Composition per liter: Agar ...................................................................1.5g NaCl ...................................................................0.5g Peptone...............................................................0.3g Beef extract ........................................................0.2g Rabbit serum ................................................ 50.0mL pH 7.9 ± 0.1 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components, except rabbit serum, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Aseptically add 50.0mL of sterile rabbit serum. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the isolation, cultivation, and maintenance of cultures of Leptospira species.
Fletcher Medium with Fluorouracil (Fluorouracil Leptospira Medium) Composition per liter: Agar ...................................................................1.5g NaCl ...................................................................0.5g Peptone...............................................................0.3g Beef extract ........................................................0.2g Rabbit serum ................................................ 50.0mL Fluorouracil solution.................................... 20.0mL pH 7.9 ± 0.1 at 25°C
Fluorouracil Solution: Composition per 100.0mL: Fluorouracil......................................................10.0g
of cultures of Leptospira species.
Fletcher’s Semisolid Medium Composition per 2120.0mL: Agar ................................................................... 1.5g NaCl................................................................... 0.5g Peptone .............................................................. 0.3g Beef extract........................................................ 0.2g Rabbit serum.............................................. 240.0mL pH 7.9 ± 0.1 at 25°C
Preparation of Medium: Add components, except rabbit serum, to distilled/deionized water and bring volume to 1880.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Aseptically add 240.0mL of sterile rabbit serum. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the isolation, cultivation, and maintenance of cultures of Leptospira species.
FLN Medium (Fluorescence Lactose Nitrate Medium) Composition per liter: Lactose............................................................. 20.0g Agar ................................................................. 15.0g Proteose peptone no. 3..................................... 10.0g KNO3 ................................................................. 2.0g K2HPO4.............................................................. 1.5g MgSO4·7H2O ..................................................... 1.5g NaNO2 ............................................................... 0.5g Phenol Red....................................................... 0.02g pH 7.2 ±0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min
206
Fluid Sabouraud Medium
at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Fluid Thioglycolate Agar with Calcium Carbonate
Use: For the differentiation of pseudomonads from
Composition per liter:
other nonfermentative bacilli. Lactose fermentation is indicated by the medium turning yellow. Pseudomonas cepacia often produces acid from lactose. Denitrification from nitrate or nitrite is indicated by the formation of gas bubbles in the solid medium. Pseudomonas aeruginosa, Pseudomonas mendocina, and Pseudomonas denitrificans are positive for denitrification. Fluorescein production is indicated by fluorescence under UV light. Pseudomonas aeruginosa is positive for fluorescein production; Pseudomonas denitrificans does not produce fluorescein.
Agar ................................................................ .75.0g Pancreatic digest of casein............................... 15.0g CaCO3 .............................................................. 10.0g Glucose .............................................................. 5.0g Yeast extract....................................................... 5.0g NaCl................................................................... 2.5g L-Cystine ............................................................ 0.5g Sodium thioglycolate ......................................... 0.5g Resazurin ....................................................... 0.001g pH 7.1 ± 0.2 at 25°C
Preparation of Medium: Add components, ex-
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
cept CaCO3, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Sterilize CaCO3 by autoclaving for 15 min at 15 psi pressure– 121°C. Aseptically add sterile CaCO3 to sterile tubes or plates—0.1g of sterile CaCO3 per 10.0mL of medium to be added. Pour medium into sterile Petri dishes or distribute into sterile tubes.
Preparation of Medium: Add components to
Use: For the rapid cultivation of anaerobic bacteria.
Fluid Sabouraud Medium Composition per liter: Glucose ............................................................20.0g Pancreatic digest of casein.................................5.0g Peptic digest of animal tissue.............................5.0g pH5.7 ± 0.2 at 25°C
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For cultivation of yeasts, molds, and aciduric microorganisms.
For the cultivation and maintenance of Campylobacter fetus, Campylobacter jejuni, Leptotrichia buccalis, and Streptococcus species.
Fluid Thioglycolate Medium Composition per liter:
Fluid Thioglycolate Agar Composition per liter: Pancreatic digest of casein...............................15.0g Glucose ..............................................................5.0g Yeast extract.......................................................5.0g NaCl ...................................................................2.5g Agar .................................................................0.75g L-Cystine ............................................................0.5g Sodium thioglycolate .........................................0.5g Resazurin ........................................................1.0mg pH 7.1 ± 0.2 at 25°C
Pancreatic digest of casein............................... 15.0g Glucose .............................................................. 5.5g Yeast extract....................................................... 5.0g NaCl................................................................... 2.5g Agar ................................................................. 0.75g L-Cystine ............................................................ 0.5g Sodium thioglycolate ......................................... 0.5g Resazurin ........................................................1.0mg pH 7.1 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to
Preparation of Medium: Add components to
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. If medium becomes oxidized before use (resazurin turns red), heat in a boiling water bath to expel absorbed O2. Cool to 25°C.
Use: For the cultivation of anaerobic bacteria. For the cultivation of Campylobacter fetus, Campylobacter jejuni, Leptotrichia buccalis, and Streptococcus species.
Use: For the cultivation of anaerobic, microaerophilic, and aerobic microorganisms. For use in sterility testing of a variety of specimens.
Fluid Thioglycolate Medium with Rabbit Serum
Fluid Thioglycolate Medium with Beef Extract
207
Fluid Thioglycolate Medium with K Agar
Composition per liter:
Composition per liter:
Pancreatic digest of casein...............................15.0g Glucose ..............................................................5.5g Yeast extract.......................................................5.0g Beef extract ........................................................5.0g NaCl ...................................................................2.5g Agar .................................................................0.75g L-Cystine ............................................................0.5g Sodium thioglycolate .........................................0.5g Resazurin ........................................................1.0mg pH 7.2 ± 0.2 at 25°C
Pancreatic digest of casein............................... 15.0g Glucose .............................................................. 5.0g Yeast extract....................................................... 5.0g KCl..................................................................... 2.5g L-Cystine ............................................................ 0.5g K agar............................................................... 0.45g Resazurin ........................................................1.0mg Thioglycolic acid ........................................... 0.3mL pH 7.2 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. If medium becomes oxidized before use (resazurin turns red), heat in a boiling water bath to expel absorbed O2. Cool to 25°C.
Use: For the cultivation of anaerobic, microaerophilic, and aerobic microorganisms. For use in sterility testing of a variety of specimens.
Fluid Thioglycolate Medium without Glucose or Eh Indicator
Composition per liter:
Pancreatic digest of casein...............................20.0g NaCl ...................................................................2.5g Agar .................................................................0.75g L-Cystine ............................................................0.5g Sodium thioglycolate .........................................0.5g pH 7.1 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Aseptically distribute into sterile screw-capped tubes or flasks.
Use: For cultivation of anaerobic bacteria. For use as a basal medium in carbohydrate fermentation tests for differentiating anaerobic bacteria. For carbohydrate fermentation tests, 1.0 mL of a 10% filter-sterilized carbohydrate solution is aseptically added to 9.0mL of fluid thioglycolate medium.
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. If medium becomes oxidized before use (resazurin turns red), heat in a boiling water bath to expel absorbed O2. Cool to 25°C.
Use: For the cultivation of anaerobic, microaerophilic, and aerobic microorganisms. For use in sterility testing of a variety of specimens.
Fluid Thioglycolate Medium with Rabbit Serum Composition per liter: Pancreatic digest of casein............................... 15.0g Glucose .............................................................. 5.5g Yeast extract....................................................... 5.0g NaCl................................................................... 2.5g Agar ................................................................. 0.75g L-Cystine ............................................................ 0.5g Sodium thioglycolate ......................................... 0.5g Resazurin ........................................................1.0mg Rabbit serum.............................................. 100.0mL pH 7.1 ± 0.2 at 25°C
Preparation of Medium: Add components, except rabbit serum, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes in 9.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C. If medium becomes oxidized before use (resazurin turns red), heat in a boiling water bath to expel absorbed O2. Cool to 25°C. Immediately prior to inoculation, aseptically and anerobically add 1.0mL of sterile rabbit serum to each tube. Mix thoroughly.
Use: For the cultivation of anaerobic, microaerophilic, and aerobic microorganisms. For use in the sterility testing of a variety of specimens.
208
Fluorocult E. coli 0157:H7 Agar
Fluorocult E. coli 0157:H7 Agar (E. coli 0157:H7 Agar, Fluorocult) Composition per liter: Peptone from casein..........................................20.0g Agar ..................................................................13.0g Sorbitol..............................................................10.0g NaCl ....................................................................5.0g Meat extract ........................................................2.0g Na2S2O3 ..............................................................2.0g Sodium deoxycholate........................................1.12g Yeast extract........................................................1.0g Ammonium ferric citrate ....................................0.5g 4-Methylumbelliferyl-β-D-glucuronide ..............0.1g Bromthymol Blue ...........................................0.025g pH 7.4 ± 0.2 at 25°C
Source: This medium is available from Merck. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Pour into sterile Petri dishes.
Use: For the isolation and differentiation of enterohemorrhagic (EHEC) Escherichia coli 0157:H7strains. In contrast to most other E. coli strains, E. coli 0157:H7 shows the following characteristics: no sorbitol-cleavage capacity within 48h. and no formation of glucuronidase (MUG-negative/no fluorescence). Sodium deoxycholate inhibits the growth of the Gram-positive accompanying flora for the greater part. Sorbitol serves, together with the pH indicator Bromthymol Blue, to determine the degradation of sorbitol which, in the case of sorbitol-positive microorganisms, results in the colonies turning yellow in color. Sorbitol-negative strains, on the other hand, do not lead to any change in the color of the culture medium and thus proliferate as greenish colonies. Sodium thiosulfate and ammonium iron(III) citrate result in black-brown discoloration of the agar for colonies, in the presence of hydrogen-sulfide-forming pathogens, precipitating iron sulfide. Proteus mirabilis in particular, which displays biochemical properties similar to those of E. coli 0157:H7, can thus be very easily differentiated from E. coli 0157:H7 on account of the brownish discoloration. 4-methylumbelliferylβ-D-glucuronide (MUG) is converted into 4-methylumbelliferone by β-D-glucuronidase-forming pathogens; 4-methylumbelliferone fluoresces under UV light. The activity of β-D-glucuronidase is a highly specific characteristic of E. coli. In contrast to most E. coli strains, E. coli 0157:H7 is not capable of forming β-D-glucoronidase. When irradiated with long-wave UV light, no fluorescence is formed.
FN Medium (Fluorescence Denitrification Medium) Composition per liter: Agar ................................................................. 15.0g Proteose peptone no. 3..................................... 10.0g KNO3 ................................................................. 2.0g K2HPO4.............................................................. 1.5g MgSO4·7H2O ..................................................... 1.5g NaNO2 ............................................................... 0.5g pH 7.2 ±0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the differentiation of pseudomonads from other nonfermentative bacilli. Denitrification from nitrate or nitrite is indicated by the formation of gas bubbles in the solid medium. Pseudomonas aeruginosa, Pseudomonas mendocina, and Pseudomonas denitrificans are positive for denitrification. Fluorescein production is indicated by fluorescence under UV light. Pseudomonas aeruginosa is positive for fluorescein production.
Folic Acid Agar Composition per liter: Noble agar........................................................ 15.0g K2HPO4·3H2O ................................................... 1.2g Folic acid ........................................................... 1.0g KH2PO4.............................................................. 0.5g Salts A............................................................ 5.0mL Salts B............................................................ 1.5mL
Salts A: Composition per 100.0mL: MgSO4·7H2O ..................................................... 1.0g CaCl2·2H2O ....................................................... 0.1g FeSO4·7H2O....................................................... 0.1g
Preparation of Salts A Solution: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Maintain for 3 days at 25°C to dissolve. Filter sterilize the supernatant.
Salts B: Composition per 100.0mL: MnSO4 ............................................................... 0.1g Na2MoO4 ........................................................... 0.1g
Preparation of Salts B Solution: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except salts A solution and salts B solution, to distilled/
FRAG Agar deionized water and bring volume to 994.5mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 5.0mL of sterile salts A solution and 1.5mL of sterile salts B solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation and maintenance of Pseudomonas species.
Formate Fumarate Medium Composition per 900.0mL: Agar .................................................................20.0g Sodium fumarate..............................................16.6g Sodium formate..................................................6.8g Yeast extract.......................................................4.0g Sodium thioglycolate solution ................... 100.0mL pH 7.3 ± 0.2 at 25°C
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Phenol Red (1% solution).............................. 1.0mL Vitamin B12 solution .................................... 0.05mL pH 7.0 ± 0.1 at 25°C
Basal Solution: Composition per 995.0mL: Oxgall .............................................................. 20.0g Agar ................................................................. 15.4g K2HPO4............................................................ 2.26g Yeast extract....................................................... 2.0g Pancreatic digest of casein................................. 1.4g (NH4)2HPO4....................................................... 1.0g K2HPO4.............................................................. 0.9g Papaic digest of soybean meal......................... 0.12g NaCl................................................................. 0.12g
Preparation of Basal Solution: Add components to distilled/deionized water and bring volume to 995.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C.
Sodium Thioglycolate Solution: Composition per 100.0mL:
Glucuronic Acid Solution: Composition per 100.0mL:
Sodium thioglycolate .........................................0.5g
D-Glucuronic
Preparation of Sodium Thioglycolate Solution: Add sodium thioglycolate to distilled/deion-
Preparation of Glucuronic Acid Solution:
ized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize. Sparge with 100% N2 gas. Warm to 50°–55°C.
Preparation of Medium: Add components, except sodium thioglycolate solution, to distilled/ deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat and bring to boiling. Continue boiling for 5 min. Cool to 50°–55°C while sparging with 80% N2 + 20% CO2. Anaerobically distribute 4.5mL volumes into anaerobic tubes. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Prior to inoculation, add 0.5mL of sterile sodium thioglycolate solution to each tube.
Use: For the cultivation and identification of Bacteroides gracilis, Bacteroides ureolyticus, Campylobacter species, and Wolinella species.
FRAG Agar (Fragilis Agar)
acid ............................................ 40.0g
Add glucuronic acid to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Gentamicin Solution: Composition per 10.0mL: Gentamicin......................................................0.1mg
Preparation of Gentamicin Solution: Add gentamicin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Vitamin K1-Hemin Solution: Composition per liter: Vitamin K1 solution ..................................... 10.0mL Hemin solution............................................. 10.0mL
Preparation of Vitamin K1-Hemin Solution:
Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
Vitamin K1 Solution: Composition per 100.0mL:
Composition per 1025.0mL:
Vitamin K1 ......................................................... 1.0g Ethanol......................................................... 99.0mL
L-Cysteine·HCl·H2O...........................................0.5g
Preparation of Vitamin K1 Solution: Add vita-
Basal solution............................................. 995.0mL Glucuronic acid solution.............................. 25.0mL Gentamicin solution....................................... 1.0mL Hemin-vitamin K1 solution............................ 1.0mL Ferric sulfate solution .................................... 1.0mL Mineral solution............................................. 1.0mL
min K1 to 99.0mL of absolute ethanol. Mix thoroughly.
Hemin Solution: Composition per 10.0mL: Hemin ................................................................ 0.5g NaOH................................................................. 0.4g
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Francisella tularensis Isolation Medium
Preparation of Hemin Solution: Add hemin and NaOH to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Ferric Sulfate Solution: Composition per 100.0mL: FeSO4·9H2O.....................................................0.04g
Preparation of Ferric Sulfate Solution: Add FeSO4·9H2O to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Mineral Solution: Composition per 100.0mL: NaCl ...................................................................9.0g CaCl2·2H2O......................................................0.27g MgCl2·6H2O ......................................................0.2g CoCl2·6H2O .......................................................0.1g MnCl2·4H2O ......................................................0.1g
Preparation of Mineral Solution: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Vitamin B12 Solution: Composition per 10.0mL: Vitamin B12 .....................................................0.1mg
Preparation of Vitamin B12 Solution: Add vitamin B12 to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: To 995.0mL of cooled, sterile basal solution, aseptically add 0.5g of L-cysteine·HCl·H2O, 25.0mL of sterile glucuronic acid solution, 1.0mL of sterile gentamicin solution, 1.0mL of sterile hemin-vitamin K1 solution, 1.0mL of sterile ferric sulfate solution, 1.0mL of sterile mineral solution, 1.0mL of Phenol Red solution, and 0.05mL of sterile vitamin B12 solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation, cultivation, and differentiation of the Bacteroides fragilis group (Bacteroides fragilis, Bacteroides thetaiotamicron, Bacteroides vulgatus, Bacteroides distasonis, Bacteriodes ovatus, and Bacteroides uniformis) from clinical specimens.
Francisella tularensis Isolation Medium Composition per liter: Agar .................................................................10.0g Glucose ............................................................10.0g Pancreatic digest of casein...............................10.0g Peptic digest of animal tissue...........................10.0g L-Cysteine·HCl·H2O ..........................................5.0g NaCl ...................................................................5.0g Sodium thioglycolate .........................................2.0g Glucose ..............................................................1.0g Thiamine·HCl .................................................5.0mg pH 7.2 ± 0.2 at 25°C
Preparation of Medium: Add components, except agar, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.2. Add agar. Gently heat and bring to boiling. Autoclave for 20 min at 15 psi pressure–121°C. Cool to 45°–50°C. Pour into sterile Petri dishes.
Use: For the isolation and cultivation of Francisella tularensis.
Freezing Medium Composition per 11.5mL: Bolton broth base........................................... 9.5mL Fetal bovine serum......................................... 1.0mL Glycerol solution ........................................... 1.0mL
Bolton Broth Base: Composition per liter: Peptone ............................................................ 10.0g Lactalbumin hydrolysate ................................... 5.0g Yeast extract....................................................... 5.0g NaCl................................................................... 5.0g α-ketoglutarate................................................... 1.0g Na-pyruvate ....................................................... 0.5g Na-metabisulfite ................................................ 0.5g Na2CO3 .............................................................. 0.6g Hemin .............................................................. 0.01g
Preparation of Bolton Broth Base: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to room temperature.
Glycerol Solution: Composition per 100.0mL: Glycerol ........................................................... 10.0g
Preparation of Glycerol Solution: Add glycerol to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to room temperature.
Preparation of Medium: Aseptically combine 9.5mL Bolton broth base, 1.0mL sterile glycerol solution, and 1.0mL filter sterilized fetal bovine serum. Mix thoroughly.
Use: For the preservation of Campylobacter spp.
G Medium Composition per liter: (NH4)2SO4 ..........................................................2.0g Yeast extract........................................................2.0g Glucose ...............................................................1.0g K2HPO4...............................................................0.6g KH2PO4...............................................................0.4g MgSO4·7H2O ......................................................0.2g CaCl2 .................................................................0.08g MnSO4·H2O ......................................................0.05g
GBNA Medium CuSO4·5H2O ....................................................5.0mg ZnSO4·7H2O ....................................................5.0mg FeSO4·7H2O.....................................................0.5mg pH 7.8 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation and maintenance of Bacillus cereus.
GAM Agar Composition per liter: GAM agar .........................................................74.0g
Source: GAM agar is available from Nissui. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of Fusobacterium necrophorum, Pediococcus species, and Peptostreptococcus spp.
GAM Semisolid Composition per liter: GAM broth........................................................74.0g Agar ....................................................................2.0g
Source: GAM broth is available from Nissui.
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NaCl....................................................................5.0g Starch ..................................................................1.0g
Source: Columbia blood agar base is available as a premixed powder from Oxoid Unipath.
Preparation of Columbia Blood Agar Base: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Antibiotic Inhibitor Solution: Composition per 10.0mL: Nalidixic acid..................................................0.035g Gentamicin sulfate ...........................................4.0mg Amphotericin B ...............................................2.0mg Ethanol............................................................ 4.0mL
Preparation of Antibiotic Inhibitor Solution: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: To 940.0mL of cooled, sterile Columbia blood agar base, aseptically add 50.0mL of rabbit or horse blood serum and 10.0mL of sterile antibiotic inhibitor solution. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the selective isolation, cultivation, and differentiation of Gardnerella vaginalis from clinical specimens, such as the vaginal discharge of patients with vaginitis. Gardnerella vaginalis exhibits βhemolysis on this medium.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of actinomycetes.
Gardnerella vaginalis Selective Medium Composition per liter: Columbia blood agar base........................... 940.0mL Rabbit or horse serum ................................... 50.0mL Antibiotic inhibitor solution.......................... 10.0mL pH 7.2 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath.
Columbia Blood Agar Base: Composition per liter: Special peptone .................................................23.0g Agar ..................................................................10.0g
GBNA Medium (Gum Base Nalidixic Acid Medium) Composition per liter: Gellan gum..........................................................8.0g Pancreatic digest of casein..................................5.7g NaCl....................................................................1.7g Papaic digest of soybean meal............................1.0g Glucose .............................................................0.83g K2HPO4.............................................................0.83g MgCl2·6H2O .....................................................0.33g Nalidixic acid....................................................0.05g pH 7.2 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to tap water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure– 121°C. Pour into sterile Petri dishes or leave in tubes.
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GBS Agar Base, Islam
Use: For the isolation and cultivation of Listeria monocytogenes from clinical and nonclinical specimens.
GBS Agar Base, Islam (Group B Streptococci Agar) (Islam GBS Agar) Composition per liter: Proteose peptone ...............................................23.0g Agar ..................................................................10.0g Na2HPO4 ...........................................................5.75g Soluble starch......................................................5.0g NaH2PO4 .............................................................1.5g Horse serum, heat inactivated....................... 50.0mL pH 7.5 ± 0.1 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath.
Preparation of Medium: Add components, except horse serum, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 50.0mL of sterile inactivated horse serum. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation and detection of group B streptococci from clinical specimens. Group B streptococci produce orange pigmented colonies when incubated under anaerobic conditions.
GBS Medium, Rapid (Group B Streptococci Medium) Starch ............................................................... 80.0g Proteose peptone ...............................................23.0g Na2HPO4 ...........................................................5.75g NaH2PO4 .............................................................1.5g Horse serum, inactivated............................... 50.0mL Antibiotic inhibitor solution......................... 10.0 mL pH 7.5 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath. Antibiotic Inhibitor Solution: Composition per 10.0mL: Metronidazole ................................................10.0mg Gentamicin.......................................................2.0mg
Preparation of Antibiotic Inhibitor Solution: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except horse serum and antibiotic inhibitor solution, to
distilled/deionized water and bring volume to 940.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C. Aseptically add 50.0mL of sterile heat-inactivated horse serum and 10.0mL of sterile antibiotic inhibitor solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks. Cool to 5°C and hold at that temperature for 12 h prior to use.
Use: For the rapid isolation and cultivation of group B streptococci from clinical specimens.
GC Agar (LMG Medium 236) Composition 1010.0mL: Solution A................................................... 500.0mL Solution B ................................................... 500.0mL Supplement solution ..................................... 10.0mL pH 7.2 ± 0.2 at 25°C
Solution A: Agar ....................................................................5.0g GC agar base, 2X........................................ 500.0mL
GC Agar Base, 2X: Composition per 500.0mL: Agar ..................................................................10.0g Pancreatic digest of casein..................................7.5g Peptic digest of animal tissue .............................7.5g NaCl....................................................................5.0g K2HPO4...............................................................4.0g Cornstarch...........................................................1.0g KH2PO4...............................................................1.0g
Source: GC agar base is available as a premixed powder from BD Diagnostic Systems. This base may be replaced by GC medium base available from BD Diagnostic Systems.
Preparation of GC Agar Base, 2X: Add components to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly.
Preparation of Solution A: Add 5.0g agar to 500.0mL GC agar base, 2X. Mix thoroughly. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Solution B: Composition per 500.0mL: Bovine hemoglobin...........................................10.0g
Preparation of Solution B: Add bovine hemoglobin to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
GC Agar Supplement Solution: Composition per liter: Glucose ...........................................................100.0g L-Cysteine·HCl..................................................25.9g L-Glutamine.......................................................10.0g L-Cystine .............................................................1.1g Adenine...............................................................1.0g Nicotinamide adenine dinucleotide ..................0.25g Vitamin B12 .........................................................0.1g Thiamine pyrophosphate.....................................0.1g Guanine·HCl .....................................................0.03g Fe(NO3)3·6H2O .................................................0.02g p-Aminobenzoic acid......................................0.013g Thiamine·HCl ..................................................3.0mg
Source: The supplement solution (IsoVitaleX enrichment) is available from BD Diagnostic Systems. This enrichment may be replaced by supplement VX from BD Diagnostic Systems.
Preparation of Supplement Solution: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
Preparation of Medium: To 500.0mL of sterile GC agar base, aseptically add 500.0mL of sterile hemoglobin solution at 45°–50°C. Mix thoroughly. Aseptically add 10.0mL of sterile supplement solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes. Use: For the cultivation and maintenance of Haemophilus parainfluenzae and Neisseria spp.
GC Agar (ATCC Medium 814) Composition per 1010.0mL: GC agar base, 2×......................................... 500.0mL Hemoglobin solution................................... 500.0mL Supplement solution ..................................... 10.0mL pH 7.2 ± 0.2 at 25°C
GC Agar Base, 2X: Composition per 500.0mL: Agar ..................................................................10.0g Pancreatic digest of casein..................................7.5g Peptic digest of animal tissue..............................7.5g NaCl ....................................................................5.0g K2HPO4 ...............................................................4.0g Cornstarch...........................................................1.0g KH2PO4 ...............................................................1.0g
Source: GC agar base is available as a premixed powder from BD Diagnostic Systems. This base may be replaced by GC medium base available from BD Diagnostic Systems.
Preparation of GC Agar Base, 2X: Add components to distilled/deionized water and bring vol-
213
ume to 500.0mL. Mix thoroughly. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C.
Hemoglobin Solution: Composition 500.0mL: Bovine hemoglobin...........................................10.0g
Preparation of Hemoglobin Solution: Add bovine hemoglobin to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Supplement Solution: Composition per liter: Glucose ...........................................................100.0g L-Cysteine·HCl..................................................25.9g L-Glutamine ......................................................10.0g L-Cystine .............................................................1.1g Adenine...............................................................1.0g Nicotinamide adenine dinucleotide ..................0.25g Vitamin B12 .........................................................0.1g Thiamine pyrophosphate ....................................0.1g Guanine·HCl .....................................................0.03g Fe(NO3)3·6H2O.................................................0.02g p-Aminobenzoic acid......................................0.013g Thiamine·HCl ..................................................3.0mg
Source: The supplement solution (IsoVitaleX enrichment) is available from BD Diagnostic Systems. This enrichment may be replaced by supplement VX from BD Diagnostic Systems.
Preparation of Supplement Solution: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
Preparation of Medium: To 500.0mL of sterile GC agar base, aseptically add 500.0mL of sterile hemoglobin solution at 45°–50°C. Mix thoroughly. Aseptically add 10.0mL of sterile supplement solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes. Use: For the isolation and cultivation of fastidious bacteria, especially Neisseria and Haemophilus species. For the cultivation and maintenance of Branhamella catarrhalis, Campylocbacter pylori, and Helicobacter pylori.
GC Agar (GC Medium) (ATCC Medium 1351) Composition per liter: GC agar base............................................... 950.0mL Blood, defibrinated ....................................... 50.0mL pH 7.2 ± 0.2 at 25°C
214
GC Agar with Ampicillin
GC Agar Base: Composition per liter: Agar ..................................................................10.0g Pancreatic digest of casein..................................7.5g Peptic digest of animal tissue..............................7.5g NaCl ....................................................................5.0g K2HPO4 ...............................................................4.0g Cornstarch...........................................................1.0g KH2PO4 ...............................................................1.0g
Source: GC agar base is available as a premixed powder from BD Diagnostic Systems. This base may be replaced by GC medium base available from BD Diagnostic Systems.
Preparation of GC Agar Base: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 75°–80°C.
Preparation of Medium: To 950.0mL of sterile GC agar base aseptically add 50.0mL sterile defibrinated blood with thorough mixing and maintain at 75°–80°C for 15–20 min until the medium is chocolatized. Pour into sterile Petri dishes or distribute into sterile tubes. Use: For the isolation and cultivation of fastidious bacteria, especially Neisseria and Haemophilus species. For the cultivation and maintenance of Branhamella catarrhalis, Campylocbacter pylori, Eikenella corrodens, Helicobacter pylori, Moraxella nonliquefaciens, Morococcus cerebrosis, Oligella ureolytica, Oligella urethralis, Pasteurella volantium, Proteus mirabilis, and Taylorella equigenitalis.
GC Agar with Ampicillin Composition per 1020.0mL: GC agar base, 2×......................................... 500.0mL Hemoglobin solution................................... 500.0mL Supplement solution ..................................... 10.0mL Ampicillin solution ....................................... 10.0mL pH 7.2 ± 0.2 at 25°C
GC Agar Base, 2X: Composition per 500.0mL: Agar ..................................................................10.0g Pancreatic digest of casein..................................7.5g Peptic digest of animal tissue..............................7.5g NaCl ....................................................................5.0g K2HPO4 ...............................................................4.0g Cornstarch...........................................................1.0g KH2PO4 ...............................................................1.0g
Source: GC agar base is available as a premixed powder from BD Diagnostic Systems. This base may be replaced by GC medium base available from BD Diagnostic Systems.
Preparation of GC Agar Base, 2X: Add components to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C.
Hemoglobin Solution: Composition per 500.0mL: Bovine hemoglobin...........................................10.0g
Preparation of Hemoglobin Solution: Add bovine hemoglobin to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Supplement Solution: Composition per liter: Glucose ...........................................................100.0g L-Cysteine·HCl..................................................25.9g L-Glutamine ......................................................10.0g L-Cystine .............................................................1.1g Adenine...............................................................1.0g Nicotinamide adenine dinucleotide ..................0.25g Vitamin B12 .........................................................0.1g Thiamine pyrophosphate ....................................0.1g Guanine·HCl .....................................................0.03g Fe(NO3)3·6H2O.................................................0.02g p-Aminobenzoic acid......................................0.013g Thiamine·HCl ..................................................3.0mg
Source: The supplement solution (IsoVitaleX enrichment) is available from BD Diagnostic Systems. This enrichment may be replaced by supplement VX from BD Diagnostic Systems.
Preparation of Supplement Solution: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
Ampicillin Solution: Composition per 10.0mL: Ampicillin .........................................................0.02g
Preparation of Ampicillin Solution: Add ampicillin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: To 500.0mL of sterile GC agar base, aseptically add 500.0mL of sterile hemoglobin solution at 45°–50°C. Mix thoroughly. Aseptically add 10.0mL of sterile supplement solution and 10.0mL of sterile ampicillin solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes. Use: For the cultivation and maintenance of Branhamella catarrhalis, Haemophilus influenzae, and Haemophilus parainfluenzae.
GC Agar with Ampicillin and Tetracycline
GC Agar with Ampicillin and Gentamicin
215
This enrichment may be replaced by supplement VX from BD Diagnostic Systems.
Composition per 1030.0mL:
Preparation of Supplement Solution: Add
GC agar base, 2×......................................... 500.0mL Hemoglobin solution................................... 500.0mL Supplement solution ..................................... 10.0mL Ampicillin solution ....................................... 10.0mL Gentamicin solution...................................... 10.0mL pH 7.2 ± 0.2 at 25°C
components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
Ampicillin Solution: Composition per 10.0mL:
GC Agar Base, 2X: Composition per 500.0mL:
ampicillin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Agar ..................................................................10.0g Pancreatic digest of casein..................................7.5g Peptic digest of animal tissue..............................7.5g NaCl ....................................................................5.0g K2HPO4 ...............................................................4.0g Cornstarch...........................................................1.0g KH2PO4 ...............................................................1.0g
Source: GC agar base is available as a premixed powder from BD Diagnostic Systems. This base may be replaced by GC medium base available from BD Diagnostic Systems.
Preparation of GC Agar Base, 2X: Add components to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C.
Hemoglobin Solution: Composition per 500.0mL: Bovine hemoglobin...........................................10.0g
Preparation of Hemoglobin Solution: Add bovine hemoglobin to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Supplement Solution: Composition per liter: Glucose ...........................................................100.0g L-Cysteine·HCl..................................................25.9g L-Glutamine.......................................................10.0g L-Cystine .............................................................1.1g Adenine...............................................................1.0g Nicotinamide adenine dinucleotide ..................0.25g Vitamin B12 .........................................................0.1g Thiamine pyrophosphate.....................................0.1g Guanine·HCl .....................................................0.03g Fe(NO3)3·6H2O .................................................0.02g p-Aminobenzoic acid......................................0.013g Thiamine·HCl ..................................................3.0mg
Source: The supplement solution (IsoVitaleX enrichment) is available from BD Diagnostic Systems.
Ampicillin .........................................................0.01g
Preparation of Ampicillin Solution: Add
Gentamicin Solution: Composition per 10.0mL: Gentamicin.......................................................2.0mg
Preparation of Gentamicin Solution: Add gentamicin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: To 500.0mL of sterile GC agar base, aseptically add 500.0mL of sterile hemoglobin solution at 45°–50°C. Mix thoroughly. Aseptically add 10.0mL of sterile supplement solution, 10.0mL of sterile ampicillin solution, and 10.0mL of sterile gentamicin solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes. Use: For the cultivation and maintenance of Haemophilus parainfluenzae.
GC Agar with Ampicillin and Tetracycline Composition per 1030.0mL: GC agar base, 2×......................................... 500.0mL Hemoglobin solution .................................. 500.0mL Supplement solution ..................................... 10.0mL Ampicillin solution ....................................... 10.0mL Tetracycline solution..................................... 10.0mL pH 7.2 ± 0.2 at 25°C
GC Agar Base, 2X: Composition per 500.0mL: Agar ..................................................................10.0g Pancreatic digest of casein..................................7.5g Peptic digest of animal tissue .............................7.5g NaCl....................................................................5.0g K2HPO4...............................................................4.0g Cornstarch...........................................................1.0g KH2PO4...............................................................1.0g
Source: GC agar base is available as a premixed powder from BD Diagnostic Systems. This base may be replaced by GC medium base available from BD Diagnostic Systems.
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GC Agar with Chloramphenicol, Tetracycline, and Ampicillin
Preparation of GC Agar Base, 2X: Add components to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C.
Hemoglobin Solution: Composition per 500.0mL: Bovine hemoglobin...........................................10.0g
Preparation of Hemoglobin Solution: Add bovine hemoglobin to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Supplement Solution: Composition per liter: Glucose ...........................................................100.0g L-Cysteine·HCl..................................................25.9g L-Glutamine.......................................................10.0g L-Cystine .............................................................1.1g Adenine...............................................................1.0g Nicotinamide adenine dinucleotide ..................0.25g Vitamin B12 .........................................................0.1g Thiamine pyrophosphate.....................................0.1g Guanine·HCl .....................................................0.03g Fe(NO3)3·6H2O .................................................0.02g p-Aminobenzoic acid......................................0.013g Thiamine·HCl ..................................................3.0mg
Source: The supplement solution (IsoVitaleX enrichment) is available from BD Diagnostic Systems. This enrichment may be replaced by supplement VX from BD Diagnostic Systems.
10.0mL of sterile tetracycline solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation and maintenance of Haemophilus parainfluenzae.
GC Agar with Chloramphenicol, Tetracycline, and Ampicillin Composition per 1040.0mL: GC agar base, 2×......................................... 500.0mL Hemoglobin solution .................................. 500.0mL Supplement solution ..................................... 10.0mL Ampicillin solution ....................................... 10.0mL Tetracycline solution..................................... 10.0mL Chloramphenicol solution............................. 10.0mL pH 7.2 ± 0.2 at 25°C
GC Agar Base, 2X: Composition per 500.0mL: Agar ..................................................................10.0g Pancreatic digest of casein..................................7.5g Peptic digest of animal tissue .............................7.5g NaCl....................................................................5.0g K2HPO4...............................................................4.0g Cornstarch...........................................................1.0g KH2PO4...............................................................1.0g
Source: GC agar base is available as a premixed powder from BD Diagnostic Systems. This base may be replaced by GC medium base available from BD Diagnostic Systems.
Preparation of GC Agar Base, 2X: Add com-
components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
ponents to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C.
Ampicillin Solution: Composition per 10.0mL:
Hemoglobin Solution: Composition per 500.0mL:
Preparation of Supplement Solution: Add
Ampicillin .........................................................0.01g
Bovine hemoglobin...........................................10.0g
Preparation of Ampicillin Solution: Add
Preparation of Hemoglobin Solution: Add bo-
ampicillin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Tetracycline Solution: Composition per 10.0mL: Tetracycline......................................................5.0mg
Preparation of Tetracycline Solution: Add tetracycline to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: To 500.0mL of sterile GC agar base, aseptically add 500.0mL of sterile hemoglobin solution at 45°–50°C. Mix thoroughly. Aseptically add 10.0mL of sterile supplement solution, 10.0mL of sterile ampicillin solution, and
vine hemoglobin to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Supplement Solution: Composition per liter: Glucose ...........................................................100.0g L-Cysteine·HCl..................................................25.9g L-Glutamine ......................................................10.0g L-Cystine .............................................................1.1g Adenine...............................................................1.0g Nicotinamide adenine dinucleotide ..................0.25g Vitamin B12 .........................................................0.1g Thiamine pyrophosphate ....................................0.1g
GC Agar with Penicillin G
217
Guanine·HCl .....................................................0.03g Fe(NO3)3·6H2O .................................................0.02g p-Aminobenzoic acid......................................0.013g Thiamine·HCl ..................................................3.0mg
K2HPO4...............................................................4.0g Cornstarch...........................................................1.0g KH2PO4...............................................................1.0g
Source: The supplement solution (IsoVitaleX en-
powder from BD Diagnostic Systems. This base may be replaced by GC medium base available from BD Diagnostic Systems.
richment) is available from BD Diagnostic Systems. This enrichment may be replaced by supplement VX from BD Diagnostic Systems.
Preparation of Supplement Solution: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
Ampicillin Solution: Composition per 10.0mL: Ampicillin .........................................................0.01g
Preparation of Ampicillin Solution: Add ampicillin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Tetracycline Solution: Composition per 10.0mL: Tetracycline......................................................5.0mg
Preparation of Tetracycline Solution: Add tetracycline to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Chloramphenicol Solution: Composition per 10.0mL: Chloramphenicol..............................................5.0mg
Preparation of Chloramphenicol Solution: Add chloramphenicol to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Source: GC agar base is available as a premixed
Preparation of GC Agar Base: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Defined Supplements Solution: Composition per 100.0mL: Glucose .............................................................40.0g Glutamine ...........................................................1.0g Fe(NO3)3·6H2O.................................................0.05g Cocarboxylase..................................................2.0mg
Preparation of Defined Supplements Solution: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: To 990.0mL of sterile GC agar base, aseptically add 10.0mL of sterile defined supplements solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes. Use: For the cultivation and maintenance of Neisseria gonorrhoeae.
GC Agar with Penicillin G
Preparation of Medium: To 500.0mL of sterile GC agar base, aseptically add 500.0mL of sterile hemoglobin solution at 45°–50°C. Mix thoroughly. Aseptically add 10.0mL of sterile supplement solution, 10.0mL of sterile ampicillin solution, 10.0mL of sterile chloramphenicol, and 10.0mL of sterile tetracycline solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Composition per 1020.0mL:
Use: For the cultivation and maintenance of Haemo-
Proteose peptone no. 3......................................15.0g Agar ..................................................................10.0g NaCl....................................................................5.0g K2HPO4...............................................................4.0g Cornstarch...........................................................1.0g KH2PO4...............................................................1.0g
philus parainfluenzae.
GC Agar with Defined Supplements GC agar base............................................... 990.0mL Defined supplements solution....................... 10.0mL pH 7.2 ± 0.2 at 25°C
GC Agar Base: Composition per liter: Agar ..................................................................10.0g Pancreatic digest of casein..................................7.5g Peptic digest of animal tissue..............................7.5g NaCl ....................................................................5.0g
GC medium base, 2× .................................. 500.0mL Hemoglobin solution .................................. 500.0mL Supplement solution ..................................... 10.0mL Penicillin G solution ..................................... 10.0mL pH 7.2 ± 0.2 at 25°C
GC Medium Base, 2X: Composition per 500.0mL:
Source: GC medium base is available as a premixed powder from BD Diagnostic Systems.
Preparation of GC Medium Base, 2X: Add components to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C.
218
GC Agar with Supplement A
Hemoglobin Solution: Composition per 500.0mL:
GC Medium Base, 2X: Composition per 500.0mL:
Bovine hemoglobin...........................................10.0g
Proteose peptone no. 3......................................15.0g Agar ..................................................................10.0g NaCl....................................................................5.0g K2HPO4...............................................................4.0g Cornstarch...........................................................1.0g KH2PO4...............................................................1.0g
Preparation of Hemoglobin Solution: Add bovine hemoglobin to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Supplement Solution: Composition per liter: Glucose ...........................................................100.0g L-Cysteine·HCl..................................................25.9g L-Glutamine.......................................................10.0g L-Cystine .............................................................1.1g Adenine...............................................................1.0g Nicotinamide adenine dinucleotide ..................0.25g Vitamin B12 .........................................................0.1g Thiamine pyrophosphate.....................................0.1g Guanine·HCl .....................................................0.03g Fe(NO3)3·6H2O .................................................0.02g p-Aminobenzoic acid......................................0.013g Thiamine·HCl ..................................................3.0mg
Source: The supplement solution (IsoVitaleX enrichment) is available from BD Diagnostic Systems. This enrichment may be replaced by supplement VX from BD Diagnostic Systems.
Preparation of Supplement Solution: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
Penicillin G Solution: Composition per 10.0mL: Penicillin G .......................................................0.05g
Preparation of Penicillin G Solution: Add penicillin G to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: To 500.0mL of sterile GC medium base, aseptically add 500.0mL of sterile hemoglobin solution at 45°–50°C. Mix thoroughly. Aseptically add 10.0mL of sterile supplement solution and 10.0mL of sterile penicillin G solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes. Use: For the cultivation and maintenance of Neisseria gonorrhoeae.
GC Agar with Supplement A Composition per 1020.0mL: GC medium base, 2× .................................. 500.0mL Hemoglobin solution................................... 500.0mL Supplement solution ..................................... 10.0mL Supplement A ............................................... 10.0mL pH 7.2 ± 0.2 at 25°C
Source: GC medium base and Supplement A are available as a premixed powder from BD Diagnostic Systems.
Preparation of GC Medium Base, 2X: Add components to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C. Hemoglobin Solution: Composition per 500.0mL: Bovine hemoglobin...........................................10.0g
Preparation of Hemoglobin Solution: Add bovine hemoglobin to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Supplement Solution: Composition per liter: Glucose ...........................................................100.0g L-Cysteine·HCl..................................................25.9g L-Glutamine ......................................................10.0g L-Cystine .............................................................1.1g Adenine...............................................................1.0g Nicotinamide adenine dinucleotide ..................0.25g Vitamin B12 .........................................................0.1g Thiamine pyrophosphate ....................................0.1g Guanine·HCl .....................................................0.03g Fe(NO3)3·6H2O.................................................0.02g p-Aminobenzoic acid......................................0.013g Thiamine·HCl ..................................................3.0mg
Source: The supplement solution (IsoVitaleX enrichment) is available from BD Diagnostic Systems. This enrichment may be replaced by supplement VX from BD Diagnostic Systems.
Preparation of Supplement Solution: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
Supplement A: Composition per 10.0mL: Supplement A contains yeast concentrate with Crystal Violet.
Preparation of Supplement A: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
GC Agar with Supplement A and with VCTN Inhibitor Preparation of Medium: To 500.0mL of sterile GC medium base, aseptically add 500.0mL of sterile hemoglobin solution at 45°–50°C. Mix thoroughly. Aseptically add 10.0mL of sterile supplement solution and 10.0mL of sterile supplement A solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes. Use: For the cultivation of Neisseria gonorrhoeae, other Neisseria species, and Haemophilus species.
GC Agar with Supplement A and with VCN Inhibitor Composition per 1030.0mL: GC medium base, 2× .................................. 500.0mL Hemoglobin solution................................... 500.0mL Supplement solution ..................................... 10.0mL Supplement A ............................................... 10.0mL VCN inhibitor ............................................... 10.0mL pH 7.2 ± 0.2 at 25°C
GC Medium Base, 2X: Composition per 500.0mL: Proteose peptone no. 3 ......................................15.0g Agar ..................................................................10.0g NaCl ....................................................................5.0g K2HPO4 ...............................................................4.0g Cornstarch...........................................................1.0g KH2PO4 ...............................................................1.0g
Source: GC medium base and Supplement A are available as a premixed powder from BD Diagnostic Systems.
Preparation of GC Medium Base, 2X: Add components to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C.
Hemoglobin Solution: Composition per 500.0mL: Bovine hemoglobin...........................................10.0g
Preparation of Hemoglobin Solution: Add bovine hemoglobin to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Supplement Solution: Composition per liter: Glucose ...........................................................100.0g L-Cysteine·HCl..................................................25.9g L-Glutamine.......................................................10.0g L-Cystine .............................................................1.1g Adenine...............................................................1.0g Nicotinamide adenine dinucleotide ..................0.25g Vitamin B12 .........................................................0.1g
219
Thiamine pyrophosphate ....................................0.1g Guanine·HCl .....................................................0.03g Fe(NO3)3·6H2O.................................................0.02g p-Aminobenzoic acid......................................0.013g Thiamine·HCl ..................................................3.0mg
Source: The supplement solution (IsoVitaleX enrichment) is available from BD Diagnostic Systems. This enrichment may be replaced by supplement VX from BD Diagnostic Systems.
Preparation of Supplement Solution: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
Supplement A: Composition per 10.0mL: Supplement A contains yeast concentrate with Crystal Violet.
Preparation of Supplement A: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
VCN Inhibitor: Composition per 10.0mL: Colistin.............................................................7.5mg Vancomycin .....................................................3.0mg Nystatin........................................................ 12,500U
Preparation of VCN Inhibitor: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: To 500.0mL of sterile GC medium base, aseptically add 500.0mL of sterile hemoglobin solution at 45°–50°C. Mix thoroughly. Aseptically add 10.0mL of sterile supplement solution, 10.0mL of sterile supplement A solution, and 10.0mL of sterile VCN inhibitor. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes. Use: For the cultivation of Neisseria gonorrhoeae, other Neisseria species, and Haemophilus species.
GC Agar with Supplement A and with VCTN Inhibitor Composition per 1030.0mL: GC medium base, 2× .................................. 500.0mL Hemoglobin solution .................................. 500.0mL Supplement solution ..................................... 10.0mL Supplement A ............................................... 10.0mL VCTN inhibitor............................................. 10.0mL pH 7.2 ± 0.2 at 25°C
GC Medium Base, 2X: Composition per 500.0mL: Proteose peptone no. 3......................................15.0g Agar ..................................................................10.0g
220
GC Agar with Supplement B
NaCl ....................................................................5.0g K2HPO4 ...............................................................4.0g Cornstarch...........................................................1.0g KH2PO4 ...............................................................1.0g
Trimethoprim lactate........................................5.0mg Vancomycin .....................................................4.0mg Nystatin........................................................ 12,500U
Source: GC medium base and Supplement A are
nents to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
available as a premixed powder from BD Diagnostic Systems.
Preparation of GC Medium Base, 2X: Add components to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C.
Hemoglobin Solution: Composition per 500.0mL: Bovine hemoglobin...........................................10.0g
Preparation of VCTN Inhibitor: Add compo-
Preparation of Medium: To 500.0mL of sterile GC medium base, aseptically add 500.0mL of sterile hemoglobin solution at 45°–50°C. Mix thoroughly. Aseptically add 10.0mL of sterile supplement solution, 10.0mL of sterile supplement A, and 10.0mL of sterile VCTN inhibitor. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes. Use: For the cultivation of Neisseria gonorrhoeae, other Neisseria species, and Haemophilus species.
Preparation of Hemoglobin Solution: Add bovine hemoglobin to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Supplement Solution: Composition per liter: Glucose ...........................................................100.0g L-Cysteine·HCl..................................................25.9g L-Glutamine.......................................................10.0g L-Cystine .............................................................1.1g Adenine...............................................................1.0g Nicotinamide adenine dinucleotide ..................0.25g Vitamin B12 .........................................................0.1g Thiamine pyrophosphate.....................................0.1g Guanine·HCl .....................................................0.03g Fe(NO3)3·6H2O .................................................0.02g p-Aminobenzoic acid......................................0.013g Thiamine·HCl ..................................................3.0mg
Source: The supplement solution (IsoVitaleX enrichment) is available from BD Diagnostic Systems. This enrichment may be replaced by supplement VX from BD Diagnostic Systems.
Preparation of Supplement Solution: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
Supplement A: Composition per 10.0mL: Supplement A contains yeast concentrate with Crystal Violet.
Preparation of Supplement A: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
VCTN Inhibitor: Composition per liter: Colistin.............................................................7.5mg
GC Agar with Supplement B GC agar base............................................... 990.0mL Supplement B................................................ 10.0mL pH 7.2 ± 0.2 at 25°C
GC Agar Base: Composition per liter: Agar ..................................................................10.0g Pancreatic digest of casein..................................7.5g Peptic digest of animal tissue .............................7.5g NaCl....................................................................5.0g K2HPO4...............................................................4.0g Cornstarch...........................................................1.0g KH2PO4...............................................................1.0g
Source: GC agar base is available as a premixed powder from BD Diagnostic Systems. This base may be replaced by GC medium base available from BD Diagnostic Systems.
Preparation of GC Agar Base: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Supplement B: Composition per 10.0mL: Supplement B contains yeast concentrate, glutamine, coenzyme, cocarboxylase, hematin, and growth factors.
Preparation of Supplement B: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. Preparation of Medium: To 990.0mL of sterile GC agar base, aseptically add 10.0mL of sterile defined supplement B. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
GCII Agar Use: For the cultivation and maintenance of Neisseria gonorrhoeae.
GC Medium, New York City Formulation Composition per liter: GC agar base............................................... 850.0mL Horse blood, lysed ...................................... 100.0mL Yeast autolysate supplement ......................... 30.0mL LCAT antibiotic solution .............................. 20.0mL pH 7.3 ± 0.2 at 25°C
GC Agar Base: Composition per 850.0mL: Special peptone .................................................15.0g Agar ..................................................................10.0g NaCl ....................................................................5.0g K2HPO4 ...............................................................4.0g Cornstarch...........................................................1.0g KH2PO4 ...............................................................1.0g pH 7.2 ± 0.2 at 25°C
Preparation of GC Agar Base: Add components of GC medium base and the hemoglobin to distilled/deionized water and bring volume to 850.0mL. Mix thoroughly. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°– 50°C.
Horse Blood, Lysed: Composition per 100.0mL: Saponin ...............................................................0.5g Horse blood, defibrinated ........................... 100.0mL
Preparation of Horse Blood, Lysed: Add saponin to defibrinated horse blood. Mix thoroughly. Allow blood to lyse.
Yeast Autolysate Supplement: Composition per 30.0mL: Yeast autolysate.................................................10.0g Glucose ...............................................................1.0g NaHCO3 ............................................................0.15g
Preparation of Yeast Autolysate Supplement: Add components to distilled/deionized water and bring volume to 30.0mL. Mix thoroughly. Filter sterilize.
LCAT Antibiotic Solution: Composition per 20.0mL: Colistin.............................................................6.0mg Trimethoprim lactate........................................5.0mg Lincomycin ......................................................1.0mg Amphotericin B................................................1.0mg
Preparation of LCAT Antibiotic Solution: Add components to distilled/deionized water and
221
bring volume to 20.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: To 850.0mL of cooled sterile GC agar base, aseptically add 100.0mL of sterile lysed horse blood, 30.0mL of sterile yeast autolysate supplement, and 20.0mL of LCAT antibiotic solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes. Use: For the selective isolation and cultivation of fastidious microorganisms, especially Neisseria species.
GCII Agar Composition per liter: GCII agar base, 2×...................................... 490.0mL Hemoglobin solution .................................. 490.0mL Supplement solution ..................................... 10.0mL pH 7.2 ± 0.2 at 25°C
GCII Agar Base, 2X: Composition per liter: Agar ..................................................................10.0g Pancreatic digest of casein..................................7.5g Selected meat peptone ........................................7.5g NaCl....................................................................5.0g K2HPO4...............................................................4.0g Cornstarch...........................................................1.0g KH2PO4...............................................................1.0g
Source: GCII agar base is available as a premixed powder from BD Diagnostic Systems. Preparation of GCII Agar Base, 2X: Add components to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C.
Hemoglobin Solution: Composition per 500.0mL: Hemoglobin ......................................................10.0g
Preparation of Hemoglobin Solution: Add hemoglobin to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Supplement Solution: Composition per liter: Glucose ...........................................................100.0g L-Cysteine·HCl..................................................25.9g L-Glutamine ......................................................10.0g L-Cystine .............................................................1.1g Adenine...............................................................1.0g Nicotinamide adenine dinucleotide ..................0.25g Vitamin B12 .........................................................0.1g Thiamine pyrophosphate ....................................0.1g Guanine·HCl .....................................................0.03g Fe(NO3)3·6H2O.................................................0.02g
222
GCII Agar
p-Aminobenzoic acid......................................0.013g Thiamine·HCl ..................................................3.0mg
Preparation of Supplement Solution: Add
Supplement solution ..................................... 10.0mL Selective agent solution ................................ 10.0mL pH 7.2 ± 0.2 at 25°C
components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
Source: This medium is available as a prepared me-
Preparation of Medium: To 490.0mL of sterile GC II agar base, aseptically add 490.0mL of sterile hemoglobin solution at 45°–50°C. Mix thoroughly. Aseptically add 10.0mL of sterile supplement solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
GCII Agar Base, 2X with Extra Agar: Composition per liter:
Use: For the isolation and cultivation of fastidious microorganisms, especially Neisseria and Haemophilus species, from clinical specimens.
GCII Agar Composition per liter: GCII agar base ............................................ 950.0mL Blood, defibrinated ....................................... 50.0mL pH 7.2 ± 0.2 at 25°C
GCII Agar Base with Extra Agar: Composition per liter: Agar ..................................................................12.0g Pancreatic digest of casein..................................7.5g Selected meat peptone ........................................7.5g NaCl ....................................................................5.0g K2HPO4 ...............................................................4.0g Cornstarch...........................................................1.0g KH2PO4 ...............................................................1.0g
dium from BD Diagnostic Systems.
Agar ..................................................................12.0g Pancreatic digest of casein..................................7.5g Selected meat peptone ........................................7.5g NaCl....................................................................5.0g K2HPO4...............................................................4.0g Cornstarch...........................................................1.0g KH2PO4...............................................................1.0g
Source: GCII agar base is available as a premixed powder from BD Diagnostic Systems. Preparation of GCII Agar Base, 2X with Extra Agar: Add components to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Hemoglobin Solution: Composition per 500.0mL: Hemoglobin ......................................................10.0g
Preparation of Hemoglobin Solution: Add hemoglobin to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Source: GCII agar base is available as a premixed powder from BD Diagnostic Systems.
Supplement Solution: Composition per liter:
Preparation of GCII Agar Base Extra Agar:
Glucose ...........................................................100.0g L-Cysteine·HCl..................................................25.9g L-Glutamine ......................................................10.0g L-Cystine .............................................................1.1g Adenine...............................................................1.0g Nicotinamide adenine dinucleotide ..................0.25g Vitamin B12 .........................................................0.1g Thiamine pyrophosphate ....................................0.1g Guanine·HCl .....................................................0.03g Fe(NO3)3·6H2O.................................................0.02g p-Aminobenzoic acid......................................0.013g Thiamine·HCl ..................................................3.0mg
Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Preparation of Medium: To 950.0mL of sterile GC agar base, aseptically add 50.0mL of sterile defibrinated blood with thorough mixing and maintain at 75°–80°C for 15–20 min until the medium is chocolatized. Pour into sterile Petri dishes or distribute into sterile tubes. Use: For the isolation and cultivation of fastidious microorganisms, especially Neisseria and Haemophilus species, from clinical specimens.
GC-Lect™ Agar
Source: The supplement solution (IsoVitaleX enrichment) is available from BD Diagnostic Systems. This enrichment may be replaced by supplement VX from BD Diagnostic Systems.
Composition per liter:
Preparation of Supplement Solution: Add
GCII agar base, 2× ...................................... 500.0mL Hemoglobin solution................................... 500.0mL
components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
GCA Agar with Thiamine Selective Agents: Composition per 10.0mL: Selective agents...............................................0.017g
Preparation of Selective Agents: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: To 500.0mL of sterile GC II agar base, aseptically add 500.0mL of sterile hemoglobin solution at 45°–50°C. Mix thoroughly. Aseptically add 10.0mL of sterile supplement solution and 10.0mL of selective agents solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes. Use: For the isolation and cultivation of Neisseria gonorrhoeae from clinical specimens.
GC Medium with Chloramphenicol
223
Supplement Solution: Composition per liter: Glucose ...........................................................100.0g L-Cysteine·HCl..................................................25.9g L-Glutamine ......................................................10.0g L-Cystine .............................................................1.1g Adenine...............................................................1.0g Nicotinamide adenine dinucleotide ..................0.25g Vitamin B12 .........................................................0.1g Thiamine pyrophosphate ....................................0.1g Guanine·HCl .....................................................0.03g Fe(NO3)3·6H2O.................................................0.02g p-Aminobenzoic acid......................................0.013g Thiamine·HCl ..................................................3.0mg
Source: The supplement solution (IsoVitaleX enrichment) is available from BD Diagnostic Systems. This enrichment may be replaced by supplement VX from BD Diagnostic Systems.
Composition per 1020.0mL:
Preparation of Supplement Solution: Add
GC agar base, 2×......................................... 500.0mL Hemoglobin solution................................... 500.0mL Supplement solution ..................................... 10.0mL Chloramphenicol solution............................. 10.0mL pH 7.2 ± 0.2 at 25°C
Chloramphenicol Solution: Composition per 10.0mL:
GC Agar Base, 2×: Composition per 500.0mL: Agar ..................................................................10.0g Pancreatic digest of casein..................................7.5g Peptic digest of animal tissue..............................7.5g NaCl ....................................................................5.0g K2HPO4 ...............................................................4.0g Cornstarch...........................................................1.0g KH2PO4 ...............................................................1.0g
Source: GC agar base is available as a premixed
components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
Chloramphenicol..............................................8.0mg
Preparation of Chloramphenicol Solution: Add chloramphenicol to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: To 500.0mL of sterile GC agar base, aseptically add 500.0mL of sterile hemoglobin solution at 45°–50°C. Mix thoroughly. Aseptically add 10.0mL of sterile supplement solution and 10.0mL of sterile chloramphenicol solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
powder from BD Diagnostic Systems. This base may be replaced by GC medium base available from BD Diagnostic Systems.
Use: For the cultivation of Neisseria gonorrhoeae.
Preparation of GC Agar Base, 2×: Add compo-
Composition per liter:
GCA Agar with Thiamine
Preparation of Hemoglobin Solution: Add bo-
Glucose .............................................................25.0g Agar ..................................................................14.0g Papaic digest of soybean meal..........................10.0g NaCl....................................................................5.0g Pancreatic digest of heart muscle .......................3.0g Cysteine·HCl·H2O ..............................................1.0g Thiamine ........................................................0.05mg Rabbit blood, defibrinated ............................ 50.0mL pH 6.8 ± 0.2 at 25°C
vine hemoglobin to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
cept rabbit blood, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15
nents to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Hemoglobin Solution: Composition per 500.0mL: Bovine hemoglobin...........................................10.0g
Preparation of Medium: Add components, ex-
224
Gelatin Agar
psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile rabbit blood. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation and cultivation of Francisella tularensis.
Gelatin Agar Composition per liter: Gelatin...............................................................30.0g Agar ..................................................................15.0g Pancreatic digest of casein................................10.0g NaCl ..................................................................10.0g pH 7.2 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of many bacteria and their differentiation based on proteolytic activity.
Gelatin Agar Composition per liter: Agar ..................................................................15.0g Gelatin...............................................................15.0g Peptone................................................................4.0g Yeast extract........................................................1.0g pH 7.2 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation of a variety of heterotrophic bacteria based upon their utilization of gelatin.
Gelatin Agar (GA Medium) Composition per liter: Solution 1.................................................... 950.0mL Solution 2...................................................... 50.0mL pH 7.2 ± 0.2 at 25°C
Solution 1: Composition per 950.0mL: Gelatin...............................................................30.0g Agar ..................................................................15.0g Pancreatic digest of casein................................10.0g NaCl ....................................................................2.0g D-Mannitol ..........................................................1.0g Glucose ...............................................................1.0g KNO3 ..................................................................1.0g
Sodium acetate....................................................1.0g Sodium formate ..................................................1.0g Sodium succinate ................................................1.0g Yeast extract........................................................1.0g Sodium lactate (60% solution)........................ 5.0mL
Preparation of Solution 1: Add components to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Solution 2: Composition per 50.0mL: Na2HPO4 .............................................................1.0g L-Cysteine·HCl·H2O............................................0.5g Na2CO3·H2O .......................................................0.5g Sucrose................................................................0.5g Dithiothreitol.......................................................0.1g Menadione solution ........................................ 2.0mL
Preparation of Solution 2: Add components to distilled/deionized water and bring volume to 50.0mL. Mix thoroughly. Filter sterilize. Menadione Solution: Composition per 100.0mL: Menadione (vitamin K3) ...................................0.05g Ethanol.......................................................... 99.0mL
Preparation of Menadione Solution: Add menadione to 99.0mL of absolute ethanol. Mix thoroughly.
Preparation of Medium: Aseptically combine sterile solution 1 with sterile solution 2. Mix thoroughly. Pour into sterile Petri dishes.
Use: For the cultivation and differentiation of microorganisms from dental plaque based on their ability to produce gelatinase. For the differentiation of aerobic, anaerobic, and facultative microorganisms of clinical significance.
Gelatin Infusion Broth Composition per liter: Beef heart, solids from infusion......................500.0g Gelatin...............................................................40.0g Tryptose ............................................................10.0g NaCl....................................................................5.0g pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Gelatin Phosphate Salt Agar
225
Use: For the cultivation and differentiation of a vari-
D-Mannitol ..........................................................1.0g
ety of heterotrophic bacteria based upon their production of gelatinase. The gelatinase liquifies the medium.
Glucose ...............................................................1.0g KNO3 ..................................................................1.0g Sodium acetate....................................................1.0g Sodium formate ..................................................1.0g Sodium succinate ................................................1.0g Yeast extract........................................................1.0g CdSO4·8H2O .....................................................0.02g Metronidazole ...................................................0.01g Sodium lactate (60% solution)........................ 5.0mL
Gelatin Medium Composition per liter: Gelatin.................................................................4.0g pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Add gelatin to distilled/ deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes. Autoclave for 15 min at 15 psi pressure– 121°C.
Use: For the cultivation and differentiation of Nocardia and Streptomyces species based on utilization of gelatin. Nocardia asteroides usually exhibits no growth. Nocardia brasiliensis shows good growth and round, compact colonies. Streptomyces species show varying degrees of growth.
Gelatin Medium Composition per liter: Gelatin.............................................................120.0g Pancreatic digest of casein................................13.0g Sodium chloride..................................................5.0g Yeast extract........................................................5.0g Heart muscle, solids from infusion .....................2.0g Sodium thioglycolate ..........................................0.5g pH 7.0 ± 0.2 at 25°C
Preparation of Solution 1: Add components to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Solution 2: Composition per 50.0mL: Na2HPO4 .............................................................1.0g L-Cysteine·HCl·H2O............................................0.5g Na2CO3·H2O .......................................................0.5g Sucrose................................................................0.5g Dithiothreitol.......................................................0.1g Menadione solution ........................................ 2.0mL
Preparation of Solution 2: Add components to distilled/deionized water and bring volume to 50.0mL. Mix thoroughly. Filter sterilize. Menadione Solution: Composition per 100.0mL: Menadione (vitamin K3) ...................................0.05g Ethanol.......................................................... 99.0mL
Preparation of Medium: Add components to
Preparation of Menadione Solution: Add me-
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
nadione to 99.0mL of absolute ethanol. Mix thoroughly.
Use: For the cultivation of gelatin-utilizing Clostrid-
Use: For the cultivation and differentiation of micro-
ium species.
Gelatin Metronidazole Cadmium Medium (GMC Medium) Composition per liter: Solution 1.................................................... 950.0mL Solution 2...................................................... 50.0mL pH 7.2 ± 0.2 at 25°C
Solution 1: Composition per 950.0mL: Gelatin...............................................................30.0g Agar ..................................................................15.0g Pancreatic digest of casein................................10.0g NaCl ....................................................................2.0g
Preparation of Medium: Aseptically combine sterile solution 1 with sterile solution 2. Mix thoroughly. Pour into sterile Petri dishes. organisms from dental plaque based on their ability to produce gelatinase. For the differentiation of aerobic, anaerobic, and facultative microorganisms of clinical significance.
Gelatin Phosphate Salt Agar (GPS Agar) Composition per liter: Agar ..................................................................15.0g Gelatin...............................................................10.0g NaCl..................................................................10.0g K2HPO4...............................................................5.0g pH 7.2 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L.
226
Gelatin Phosphate Salt Broth
Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes.
Preparation of L-Cysteine·HCl·H2O Solution:
Use: For the cultivation and differentiation of Vibrio
Fe4(P2O7)3 Solution: Composition per 10.0mL:
species.
Gelatin Phosphate Salt Broth (GPS Broth) Composition per liter: Gelatin...............................................................10.0g NaCl ..................................................................10.0g K2HPO4 ...............................................................5.0g pH 7.2 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of Vibrio species.
Gelatin Salt Agar Composition per liter: NaCl ..................................................................30.0g Agar ..................................................................15.0g Gelatin...............................................................15.0g Peptone................................................................4.0g Yeast extract........................................................1.0g pH 7.2 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and differentiation of Vibrio species.
Add L-cysteine·HCl·H2O to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Fe4(P2O7)3 .........................................................0.15g
Preparation of Fe4(P2O7)3 Solution: Add Fe4(P2O7)3 to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. Preparation of Medium: Add ACES buffer to distilled/deionized water and bring volume to 899.0mL. Mix thoroughly. Gently heat to 50°C. Add 1.0mL of KOH solution. Mix thoroughly. Add charcoal, yeast extract and α-ketoglutarate. Add 80.0mL of distilled/deionized water to wash sides of flask. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C. Aseptically add 10.0mL of sterile cysteine solution and 10.0mL of sterile Fe4(P2O7)3 solution. Mix thoroughly. Adjust pH to 6.9. Aseptically distribute into sterile screw-capped tubes.
Use: For the cultivation and differentiation of gelatinase-producing bacteria.
Gluconate Peptone Broth Composition per liter: Potassium gluconate .........................................40.0g Casein peptone....................................................1.5g K2HPO4...............................................................1.0g Yeast extract........................................................1.0g pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation and differentiation of Gram-
Gelatinase Test Medium Composition per liter: Gelatin.................................................................3.0g ACES buffer........................................................1.0g Yeast extract........................................................1.0g Charcoal, activated............................................0.15g α-Ketoglutarate monopotassium salt ..................0.1g L-Cysteine·HCl·H2O (4% solution)................. 1.0mL KOH (85% solution) ....................................... 1.0mL Fe4(P2O7)3 solution ......................................... 1.0mL pH 6.9 ± 0.2 at 25°C L-Cysteine·HCl·H2O
Solution: Composition per 10.0mL: L-Cysteine·HCl·H2O............................................0.4g
negative bacteria based on their ability to oxidize gluconate to 2-ketogluconate. For the differentiation of fluorescent Pseudomonas species. After inoculation with bacteria and 48 hr of growth in this medium, Benedict’s reagent is added. Bacteria that produce the reducing sugar 2-ketogluconate turn the reagent yellow-orange to orange-red.
Glucose Nutrient Agar Composition per liter: Agar ..................................................................15.0g Pancreatic digest of casein................................10.0g Glucose ...............................................................5.0g K2HPO4...............................................................5.0g
Glutarate Medium NaCl ....................................................................5.0g Yeast extract........................................................5.0g
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the isolation and cultivation of Brochothrix thermosphacta.
Glucose Phosphate Broth Composition per liter: Peptone..............................................................10.0g K2HPO4 ...............................................................5.0g Glucose ...............................................................5.0g pH 7.5 ± 0.2 at 25°C
Preparation of Medium: Add components, except glucose, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Filter while hot through Whatman filter paper. Cool to 25°C. Adjust pH to 7.5. Add 5.0g of glucose. Mix thoroughly. Distribute into sterile tubes or flasks. Autoclave for 10 min at 10 psi pressure–115°C.
Use: For the cultivation of a variety of nonfastidious heterotrophic microorganisms.
Glucose Salt Teepol Broth (GSTB) Composition per liter: NaCl ..................................................................30.0g Peptone..............................................................10.0g Glucose ...............................................................5.0g Beef extract .........................................................3.0g Methyl Violet ...................................................2.0mg Sodium lauryl sulfate (Teepol—0.1% solution) .......................... 4.0mL pH 8.8 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 8.8. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of Vibrio species.
Glucose Salts Medium Composition per 1000.5mL: Glucose ...............................................................5.0g (NH4)2SO4...........................................................1.0g MgSO4·7H2O ......................................................0.5g NaCl ....................................................................0.5g NaH2PO4·12H2O..............................................0.7mg
227
NaH2PO4·2H2O................................................0.3mg Trace elements solution .................................. 0.5mL pH 6.9 ± 0.2 at 25°C
Trace Elements Solution: Composition per liter: H3BO3 .................................................................0.3g CoCl2·6H2O ........................................................0.2g ZnSO4·7H2O .......................................................0.1g MnCl2·4H2O .....................................................0.03g Na2MoO4·2H2O ................................................0.03g NiCl2·6H2O .......................................................0.02g CuCl2·2H2O ......................................................0.01g
Preparation of Trace Elements Solution: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except trace elements solution, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Aseptically add 0.5mL of sterile trace elements solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation of a wide variety of bacteria and fungi.
Glutarate Medium Composition per liter: Sodium glutarate.................................................2.6g NaCl....................................................................1.0g KCl......................................................................0.5g MgCl2·6H2O .......................................................0.4g NH4Cl ...............................................................0.25g KH2PO4...............................................................0.2g CaCl2·2H2O ......................................................0.15g Resazurin .........................................................1.0mg Rumen fluid .................................................. 20.0mL NaHCO3 solution .......................................... 20.0mL Na2S·9H2O solution...................................... 10.0mL Trace elements solution SL-10 ....................... 1.0mL pH 7.2 ± 0.2 at 25°C
Trace Elements Solution SL-10: Composition per liter: FeCl2·4H2O .........................................................1.5g CoCl2·6H2O .................................................190.0mg MnCl2·4H2O ................................................100.0mg ZnCl2 ..............................................................70.0mg Na2MoO4·2H2O .............................................36.0mg NiCl2·6H2O ....................................................24.0mg H3BO3 ..............................................................6.0mg CuCl2·2H2O .....................................................2.0mg HCl (25% solution)....................................... 10.0mL
Preparation of Trace Elements Solution SL-10: Add FeCl2·4H2O to 10.0mL of HCl solution. Mix
228
Glycerol Agar
thoroughly. Add distilled/deionized water and bring volume to 1.0L. Add remaining components. Mix thoroughly. Gas under 80% N2 + 20% CO2. Autoclave for 15 min at 15 psi pressure–121°C.
NaHCO3 Solution: Composition per 20.0mL: NaHCO3 ..............................................................2.5g
Preparation of NaHCO3 Solution: Add NaHCO3 to distilled/deionized water and bring volume to 20.0mL. Mix thoroughly. Filter sterilize. Gas under 80% N2 + 20% CO2.
Na2S·9H2O Solution: Composition per 10.0mL: Na2S·9H2O........................................................0.36g
Preparation of Na2S·9H2O Solution: Add 0.36g
Glycerol Asparagine Meat Agar Composition per liter: Agar ..................................................................20.0g Glycerol ............................................................10.0g Beef extract.......................................................10.0g L-Asparagine .......................................................1.0g K2HPO4...............................................................1.0g Trace salts solution ......................................... 1.0mL pH 7.4 ± 0.2 at 25°C
Trace Salts Solution: Composition per 100.0mL: FeSO4·7H2O........................................................0.1g MnCl2·4H2O .......................................................0.1g ZnSO4·7H2O .......................................................0.1g
Preparation of Trace Salts Solution: Add com-
Na2S·9H2O to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Gas under 100% N2. Autoclave for 15 min at 15 psi pressure–121°C.
ponents to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Prepare and dispense
cept trace salts solution, to distilled/deionized water and bring volume to 999.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 1.0mL of sterile trace salts solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
medium under 80% N2 + 20% CO2. Add components, except NaHCO3 solution and Na2S·9H2O solution, to distilled/deionized water and bring volume to 970.0mL. Mix thoroughly. Sparge with 80% N2 + 20% CO2. Autoclave for 15 min at 15 psi pressure–121°C. Aseptically and anaerobically add 20.0mL of sterile NaHCO3 solution and 10.0mL of sterile Na2S·9H2O solution. Mix thoroughly. Aseptically and anaerobically distribute into sterile tubes or flasks.
Use: For the cultivation of a wide variety of bacteria. that can utilize glutarate as a carbon source.
Glycerol Agar Composition per liter: Beef heart, infusion from ................................300.0g Glycerol ............................................................60.0g Agar ..................................................................17.5g Tryptose ..............................................................7.0g NaCl ....................................................................3.0g Peptone................................................................2.5g NaCl ....................................................................2.5g Yeast extract........................................................1.0g Beef extract .........................................................0.5g pH 7.3 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.3. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation of fastidious bacteria.
Preparation of Medium: Add components, ex-
Use: For the cultivation of Actinomadura species and Streptomyces species.
GN Broth, Hajna Composition per liter: Pancreatic digest of casein................................10.0g Peptic digest of animal tissue ...........................10.0g NaCl....................................................................5.0g Sodium citrate.....................................................5.0g K2HPO4...............................................................4.0g D-Mannitol ..........................................................2.0g KH2PO4...............................................................1.5g Glucose ...............................................................1.0g Sodium deoxycholate..........................................0.5g pH 7.0 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 13 psi pressure–118°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the selective cultivation of Salmonella and Shigella species.
Granada Medium
Gonococcus Medium Composition per 623.0mL: Part II .......................................................... 500.0mL Part I............................................................ 123.0mL pH 7.4 ± 0.2 at 25°C
Part I: Composition per 123.0mL: K2HPO4 .............................................................10.5g Glucose ...............................................................7.5g NaCl ..................................................................5.25g KH2PO4 ...............................................................4.5g Sodium acetate....................................................1.5g L-Cysteine·HCl·H2O............................................1.2g Sodium citrate ...................................................1.13g NaHCO3 ..............................................................1.0g K2SO4..................................................................0.9g Na2SO4 ..............................................................0.75g MgCl2·6H2O .....................................................0.45g KCl......................................................................0.3g NH4Cl .................................................................0.3g L-Arginine·HCl..................................................0.25g L-Proline ............................................................0.25g Oxaloacetate......................................................0.25g L-Glutamic acid .................................................0.19g L-Methionine .....................................................0.19g L-Asparagine·H2O .............................................0.13g L-Isoleucine .......................................................0.13g L-Serine .............................................................0.13g L-Cystine ...........................................................0.05g Calcium pantothenate .......................................0.02g Thiamine·HCl ...................................................0.02g Thiamine pyrophosphate chloride ....................0.02g Nicotinamide adenine dinucleotide ..................0.01g CaCl2·2H2O......................................................5.0mg Fe(NO3)3·9H2O ................................................5.0mg Uracil ...............................................................5.0mg Biotin ...............................................................4.0mg Hypoxanthine...................................................2.5mg Sodium thioglycolate ...................................0.025mg
Preparation of Part I: Add components to distilled/deionized water and bring volume to 123.0mL. Mix thoroughly. Adjust pH to 7.2 with 6N NaOH. Warm to 50°C for 45 min. Filter sterilize.
Part II: Composition per 500.0mL: Agar ..................................................................10.0g Soluble starch......................................................7.5g
Preparation of Part II: Add components to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
229
Preparation of Medium: Aseptically combine 123.0mL of sterile part I and 500.0mL of cooled, sterile part II. Mix thoroughly. Pour into sterile Petri dishes.
Use: For the cultivation of Neisseria gonorrhoeae.
GP Agar (Glycerol Peptone Agar) Composition per liter: Agar ..................................................................15.0g Peptone .............................................................10.0g Glycerol ............................................................10.0g
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation of actinomycetes and Mycobacterium spp.
GPHF Agar Composition per liter: Agar ..................................................................12.0g Glucose .............................................................10.0g Beef extract.........................................................5.0g Pancreatic digest of casein..................................5.0g Yeast extract........................................................5.0g CaCl2·2H2O ......................................................0.74g pH 7.2 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of Actinoplanes caeruleus, Micromonospora species, Microtetraspora fusca, and Streptomyces yerevanensis.
Granada Medium Composition per liter: Starch, soluble.................................................150.0g Proteose peptone no. 3......................................38.0g NaCl....................................................................3.0g Trimethoprim lactate.......................................0.015g Sodium phosphate buffer (0.06M, pH 7.4) ......................... 900.0mL Horse serum, coagulated............................. 100.0mL pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add proteose peptone no. 3 and NaCl to 200.0mL of sodium phosphate buffer and bring to boiling. Add 400.0mL of cold sodium
230
Group A Selective Strep Agar with Sheep Blood
phosphate buffer, starch, and trimethoprim lactate. Mix thoroughly. Bring volume to 900.0mL with sodium phosphate buffer. Gently heat while stirring in a boiling water bath for exactly 20 min. Do not autoclave. Cool to 90°–95°C. Add horse serum. Mix thoroughly. Cool to 60°–65°C while stirring. Pour into sterile Petri dishes. Medium will solidify in 2–3h.
Use: For the early selective isolation and cultivation of Group B streptococci from clinical specimens.
Group A Selective Strep Agar with Sheep Blood Composition per liter: Pancreatic digest of casein................................14.5g Agar ..................................................................14.0g NaCl ....................................................................5.0g Papaic digest of soybean meal ............................5.0g Sheep blood................................................... 50.0mL Growth factor solution .................................. 10.0mL Selective agents solution............................... 10.0mL pH 7.4 ± 0.2 at 25°C
Growth Factor Solution: Composition per 10.0mL: Growth factors, BD Diagnostic Systems ............1.5g
Preparation of Growth Factor Solution: Add growth factors to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Selective Agent Solution: Composition per 10.0mL: Selective agents...............................................0.042g
Preparation of Selective Agent Solution: Add selective agents to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except sheep blood, growth factor solution, and selective agent solution, to distilled/deionized water and bring volume to 930.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 50.0mL of sheep blood, 10.0mL of sterile growth factor solution, and 10.0mL of sterile selective agent components. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the selective cultivation and primary isolation of group A streptococci, especially Streptococcus pyogenes from clinical specimens.
H Agar Composition per liter: Agar ..................................................................15.0g Pancreatic digest of casein................................10.0g NaCl ....................................................................8.0g
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of Escherichia coli and a variety of other bacteria.
H Agar (Hominis Agar) Composition per 98.0mL: Base agar....................................................... 65.0mL Horse serum .................................................. 20.0mL Yeast dialysate .............................................. 10.0mL Penicillin solution ........................................... 2.0mL Thallium acetate solution................................ 1.0mL pH 7.3 ± 0.2 at 25°C
Base Agar: Composition per liter: Papaic digest of soybean meal..........................20.0g Agarose .............................................................10.0g NaCl....................................................................5.0g Phenol Red (2% solution)............................... 1.0mL
Preparation of Base Agar: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Adjust pH to 7.3. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Yeast Dialysate: Composition per 10.0mL: Active, dried yeast ..........................................450.0g
Preparation of Yeast Dialysate: Add active, dried yeast to distilled/deionized water and bring volume to 1250.0mL. Gently heat and bring to 40°C. Autoclave for 15 min at 15 psi pressure–121°C. Put into dialysis tubing. Dialyze against 1.0L of distilled/ deionized water for 2 days at 4°C. Discard tubing and its contents. Autoclave dialysate for 15 min at 15 psi pressure–121°C. Store at −20°C. Penicillin Solution: Composition per 10.0mL: Penicillin .................................................... 100,000U
Preparation of Penicillin Solution: Add penicillin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Thallium Acetate Solution: Composition per 10.0mL: Thallium acetate................................................0.33g
H Broth Caution: Thallium salts are toxic. Preparation of Thallium Acetate Solution:
231
Adjust pH to 7.3. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C.
Add thallium acetate to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Yeast Dialysate: Composition per 10.0mL:
Preparation of Medium: To 65.0mL of cooled,
Preparation of Yeast Dialysate: Add active, dried yeast to distilled/deionized water and bring volume to 1250.0mL. Gently heat and bring to 40°C. Autoclave for 15 min at 15 psi pressure–121°C. Put into dialysis tubing. Dialyze against 1.0L of distilled/ deionized water for 2 days at 4°C. Discard tubing and its contents. Autoclave dialysate for 15 min at 15 psi pressure–121°C. Store at −20°C.
sterile base agar, aseptically add 10.0mL of sterile yeast dialysate, 20.0mL of horse serum, 2.0mL of sterile penicillin solution, and 1.0mL of sterile thallium acetate solution. Mix thoroughly. Pour into 10mm × 35mm Petri dishes in 5.0mL volumes. Allow plates to stand overnight at 25°C to remove excess surface moisture.
Use: For the isolation of Mycoplasma pneumoniae and Mycoplasma hominis.
H Broth Composition per liter: NaCl ....................................................................5.0g Pancreatic digest of casein..................................5.0g Peptone................................................................5.0g Beef extract .........................................................3.0g K2HPO4 ...............................................................2.5g Glucose ...............................................................1.0g pH 7.2 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes in 4.0mL volumes. Autoclave for 15 min at 10 psi pressure– 115°C.
Use: For the preparation of the H agglutination anti-
Dried yeast, active ..........................................450.0g
Penicillin Solution: Composition per 10.0mL: Penicillin .................................................... 100,000U
Preparation of Penicillin Solution: Add penicillin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Glucose Solution: Composition per 10.0mL: D-Glucose ............................................................1.8g
Preparation of Glucose Solution: Add
D-glucose to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Caution: Thallium salts are toxic. Thallium Acetate Solution: Composition per 10.0mL: Thallium acetate................................................0.33g
gen used in the differentiation and identification of Salmonella species types and subtypes.
Preparation of Thallium Acetate Solution: Add thallium acetate to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
H Broth (Hominis Broth)
Preparation of Medium: To 65.0mL of cooled,
Composition per 99.0mL: Base broth ..................................................... 65.0mL Horse serum .................................................. 20.0mL Yeast dialysate............................................... 10.0mL Penicillin solution ........................................... 2.0mL Glucose solution ............................................. 1.0mL Thallium acetate solution................................ 1.0mL pH 7.3 ± 0.2 at 25°C
Base Broth: Composition per liter: Papaic digest of soybean meal ..........................20.0g NaCl ....................................................................5.0g Phenol Red (2% solution) ............................... 1.0mL
Preparation of Base Broth: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling.
sterile base broth, aseptically add 10.0mL of sterile yeast dialysate, 20.0mL of horse serum, 2.0mL of sterile penicillin solution, 1.0mL of sterile glucose solution, and 1.0mL of sterile thallium acetate solution. Mix thoroughly. Aseptically distribute into sterile screw-capped tubes in 5.0mL volumes. Screw caps down tightly.
Use: For the isolation and cultivation of Mycoplasma pneumoniae.
H Broth (Hominis Broth) Composition per 100.0mL: Base broth ..................................................... 65.0mL Horse serum .................................................. 20.0mL Yeast dialysate .............................................. 10.0mL Penicillin solution ........................................... 2.0mL
232
H Diphasic Medium
Arginine solution ............................................ 2.0mL Thallium acetate solution................................ 1.0mL pH 7.3 ± 0.2 at 25°C
ile screw-capped tubes in 5.0mL volumes. Screw caps down tightly.
Base Broth: Composition per liter:
ma hominis.
Papaic digest of soybean meal ..........................20.0g NaCl ....................................................................5.0g Phenol Red (2% solution) ............................... 1.0mL
Preparation of Base Broth: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Adjust pH to 7.3. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C.
Yeast Dialysate: Composition per 10.0mL: Dried yeast, active...........................................450.0g
Preparation of Yeast Dialysate: Add active, dried yeast to distilled/deionized water and bring volume to 1250.0mL. Gently heat and bring to 40°C. Autoclave for 15 min at 15 psi pressure–121°C. Put into dialysis tubing. Dialyze against 1.0L of distilled/ deionized water for 2 days at 4°C. Discard tubing and its contents. Autoclave dialysate for 15 min at 15 psi pressure–121°C. Store at −20°C.
Penicillin Solution: Composition per 10.0mL: Penicillin ....................................................100,000U
Preparation of Penicillin Solution: Add penicillin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Arginine Solution: Composition per 10.0mL:
Use: For the isolation and cultivation of Mycoplas-
H Diphasic Medium Composition per 197.0mL: Base agar....................................................... 65.0mL Base broth ..................................................... 65.0mL Horse serum .................................................. 40.0mL Yeast dialysate .............................................. 20.0mL Penicillin solution ........................................... 4.0mL Thallium acetate solution................................ 2.0mL Glucose solution ............................................. 1.0mL pH 7.3 ± 0.2 at 25°C
Base Agar: Composition per liter: Papaic digest of soybean meal..........................20.0g Agarose .............................................................10.0g NaCl....................................................................5.0g Phenol Red (2% solution)............................... 1.0mL
Preparation of Base Agar: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Adjust pH to 7.3. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Base Broth: Composition per liter: Papaic digest of soybean meal..........................20.0g NaCl....................................................................5.0g Phenol Red (2% solution)............................... 1.0mL
nine to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Base Broth: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Adjust pH to 7.3. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C.
Thallium Acetate Solution: Composition per 10.0mL:
Yeast Dialysate: Composition per 10.0mL:
Thallium acetate................................................0.33g
Dried yeast, active ..........................................450.0g
Caution: Thallium salts are toxic.
Preparation of Yeast Dialysate: Add active, dried yeast to distilled/deionized water and bring volume to 1250.0mL. Gently heat and bring to 40°C. Autoclave for 15 min at 15 psi pressure–121°C. Put into dialysis tubing. Dialyze against 1.0L of distilled/ deionized water for 2 days at 4°C. Discard tubing and its contents. Autoclave dialysate for 15 min at 15 psi pressure–121°C. Store at −20°C.
L-Arginine .........................................................1.74g
Preparation of Arginine Solution: Add L-argi-
Preparation of Thallium Acetate Solution: Add thallium acetate to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: To 65.0mL of cooled, sterile base broth, aseptically add 10.0mL of sterile yeast dialysate, 20.0mL of horse serum, 2.0mL of sterile penicillin solution, 1.0mL of sterile glucose solution, and 1.0mL of sterile thallium acetate solution. Mix thoroughly. Aseptically distribute into ster-
Penicillin Solution: Composition per 10.0mL: Penicillin .................................................... 100,000U
Haemophilus ducreyi Medium, Revised Preparation of Penicillin Solution: Add penicillin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Glucose Solution: Composition per 10.0mL:
heat until boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Fresh Yeast Extract Solution: Composition per 100.0mL: Baker’s yeast, live, pressed, starch-free............25.0g
D-Glucose ............................................................1.8g
Preparation of Glucose Solution: Add
233
D-glu-
cose to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Thallium Acetate Solution: Composition per 10.0mL:
Preparation of Fresh Yeast Extract Solution: Add the live Baker’s yeast to 100.0mL of distilled/ deionized water. Autoclave for 90 min at 15 psi pressure–121°C. Allow to stand. Remove supernatant solution. Adjust pH to 6.6–6.8. Filter sterilize.
Caution: Thallium salts are toxic.
Preparation of Medium: To 675.0mL of cooled, sterile Columbia blood agar base, aseptically add rabbit blood and sterile fresh yeast extract solution. Aseptically adjust pH to 6.5–7.0.
Preparation of Thallium Acetate Solution:
Use: For the cultivation and maintenance of Haemo-
Thallium acetate................................................0.33g
Add thallium acetate to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: To 65.0mL of cooled, sterile base agar, aseptically add 10.0mL of sterile yeast dialysate, 20.0mL of horse serum, 2.0mL of sterile penicillin solution, and 1.0mL of sterile thallium acetate solution. Mix thoroughly. Aseptically distribute into screw-capped tubes in 3.0mL volumes. Allow agar to solidify. To 65.0mL of cooled, sterile base broth, aseptically add 10.0mL of sterile yeast dialysate, 20.0mL of horse serum, 2.0mL of sterile penicillin solution, 1.0mL of sterile glucose solution, and 1.0mL of sterile thallium acetate solution. Mix thoroughly. Aseptically distribute 3.0mL of broth solution on top of the 3.0mL of solidified base agar in each tube. Screw caps down tightly.
Use: For the isolation and cultivation of Mycoplasma pneumoniae.
Haemophilus ducreyi Medium Composition per liter: Columbia blood agar base........................... 675.0mL Rabbit blood................................................ 300.0mL Fresh yeast extract solution........................... 25.0mL pH 6.5–7.0 at 25°C
Columbia Blood Agar Base: Composition per 675.0mL: Agar ..................................................................15.0g Pantone..............................................................10.0g Bitone................................................................10.0g NaCl ....................................................................5.0g Tryptic digest of beef heart .................................3.0g Cornstarch...........................................................1.0g
philus ducreyi.
Haemophilus ducreyi Medium, Revised (Ducreyi Medium, Revised) Composition per 1010.0mL: Solution B ................................................... 500.0mL Solution A................................................... 400.0mL Solution C ................................................... 110.0mL pH 7.4 ± 0.2 at 25°C
Solution A: Composition per 400.0mL: Beef heart, infusion from................................500.0g Agar ..................................................................15.0g Tryptose ............................................................10.0g NaCl....................................................................5.0g
Preparation of Solution A: Add components to distilled/deionized water and bring volume to 400.0L. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C.
Solution B: Composition per 500.0mL: Hemoglobin ......................................................10.0g
Preparation of Solution B: Add components to distilled/deionized water and bring volume to 500.0L. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C.
Solution C: Composition per 110.0mL: Fetal bovine serum...................................... 100.0mL Supplement solution ..................................... 10.0mL
Preparation of Columbia Blood Agar Base:
Supplement Solution: Composition per liter:
Add components to distilled/deionized water and bring volume to 675.0mL. Mix thoroughly. Gently
Glucose ...........................................................100.0g L-Cysteine·HCl .................................................25.9g
234
Haemophilus influenzae Defined Medium MI
L-Glutamine ......................................................10.0g L-Cystine .............................................................1.1g
Adenine...............................................................1.0g Nicotinamide adenine dinucleotide ..................0.25g Vitamin B12 .........................................................0.1g Thiamine pyrophosphate.....................................0.1g Guanine·HCl .....................................................0.03g Fe(NO3)3·6H2O .................................................0.02g p-Aminobenzoic acid......................................0.013g Thiamine·HCl ..................................................3.0mg
Source: The supplement solution (IsoVitaleX en-
Polyvinyl alcohol ..............................................0.02g Tween 80...........................................................0.02g Hemin ...............................................................0.01g L-Histidine.........................................................0.01g Calcium pantothenate ......................................4.0mg Ethylenediaminetetraacetate ............................4.0mg Nicotinamide adenine dinucleotide .................4.0mg Thiamine ..........................................................4.0mg
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
richment) is available from BD Diagnostic Systems. This enrichment may be replaced by supplement VX from BD Diagnostic Systems.
Use: For the cultivation of Haemophilus influenzae
Preparation of Supplement Solution: Add
Haemophilus influenzae Defined Medium MI-Cit
components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
Preparation of Solution C: Combine components. Mix thoroughly. Filter sterilize. Warm to 45°–50°C.
Preparation of Medium: Aseptically combine solution A, solution B, and solution C. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation and maintenance of Haemophilus ducreyi.
Haemophilus influenzae Defined Medium MI Composition per liter: NaCl ....................................................................5.8g K2HPO4 ...............................................................3.5g Glycerol ..............................................................3.0g KH2PO4 ...............................................................2.7g Inosine.................................................................2.0g L-Glutamic acid ...................................................1.3g K2SO4..................................................................1.0g Sodium lactate.....................................................0.8g L-Aspartic acid ....................................................0.5g Nitrilotriethanol ..................................................0.4g L-Arginine ...........................................................0.3g L-Leucine.............................................................0.3g L-Cystine .............................................................0.2g MgCl2 ..................................................................0.2g L-Tyrosine............................................................0.2g L-Methionine .......................................................0.1g L-Serine ...............................................................0.1g Uracil ..................................................................0.1g L-Lysine.............................................................0.05g Glycine..............................................................0.03g CaCl2 ...............................................................0.022g Hypoxanthine....................................................0.02g
in a chemically defined medium.
Composition per liter: NaCl....................................................................5.8g K2HPO4...............................................................3.5g Glycerol ..............................................................3.0g KH2PO4...............................................................2.7g Inosine.................................................................2.0g L-Glutamic acid...................................................1.3g K2SO4 .................................................................1.0g Sodium lactate ....................................................0.8g L-Aspartic acid ....................................................0.5g Nitrilotriethanol ..................................................0.4g L-Leucine ............................................................0.3g L-Cystine .............................................................0.2g MgCl2..................................................................0.2g L-Tyrosine ...........................................................0.2g Citrulline ...........................................................0.15g L-Methionine .......................................................0.1g L-Serine ...............................................................0.1g L-Lysine.............................................................0.05g Glycine..............................................................0.03g CaCl2 ...............................................................0.022g Hypoxanthine....................................................0.02g Polyvinyl alcohol ..............................................0.02g Tween 80...........................................................0.02g Hemin ...............................................................0.01g L-Histidine.........................................................0.01g Calcium pantothenate ......................................4.0mg Ethylenediaminetetraacetate ............................4.0mg Nicotinamide adenine dinucleotide .................4.0mg Thiamine ..........................................................4.0mg
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
Use: For the cultivation of Haemophilus influenzae in a chemically defined medium.
Haemophilus Test Medium
Haemophilus Medium (DSMZ Medium 804)
235
pH to 8.0. Filter through a Seitz filter. Store at -20°C. Check sterility before using.
Composition per liter:
Preparation of Medium: Add components, ex-
Acid hydrolysate of casein................................31.5g Beef extract .........................................................5.4g Yeast extract........................................................5.0g Starch ..................................................................2.7g NAD solution.................................................. 1.0mL Hemin solution................................................ 1.0mL pH 7.3 ± 0.1 at 25°C
cept yeast extract solution and horse serum, to distilled/deionized water and bring volume to 850.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Aseptically add 100.0mL of sterile yeast extract solution and 50.0mL of sterile horse serum. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
NAD Solution: Composition per 10.0mL: NAD.............................................................150.0mg
Preparation of NAD Solution: Add NAD to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Hemin Solution: Composition per 10.0mL: Hemin...........................................................150.0mg NaOH (1N solution)........................................ 2.0mL
Preparation of Hemin Solution: Add hemin to 2.0mL of 1N NaOH solution. Mix thoroughly. Bring volume to 10.0mL with distilled/deionized water. Filter sterilize.
Use: For the cultivation and maintenance of Actinobacillus pleuropneumoniae and Haemophilus spp.
Haemophilus Test Medium (HTM) Composition per liter: Beef infusion...................................................300.0g Acid hydrolysate of casein................................17.5g Agar ..................................................................17.0g Yeast extract........................................................5.0g Starch ..................................................................1.5g HTM supplement .......................................... 10.0mL pH 7.4 ± 0.2 at 25°C
Source: This medium is available as a premixed
Preparation of Medium: Add components, ex-
powder from Oxoid Unipath.
cept hemin solution and NAD solution, to distilled/ deionized water and bring to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 10 min at 10 psi pressure–115°C. Cool to 25°C. Aseptically add 1.0mL sterile NAD solution and 1.0mL sterile hemin solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
HTM Supplement: Composition per 10.0mL:
Use: For the cultivation of Haemophilus influenzae.
Haemophilus Medium Composition per 1050.0mL: Beef heart, infusion from ..................................25.0g Agar ..................................................................14.0g Peptone................................................................5.0g NaCl ....................................................................2.5g Glucose ...............................................................1.0g Yeast extract solution .................................. 100.0mL Horse serum .................................................. 50.0mL
Yeast Extract Solution: Composition per liter: Baker’s yeast...................................................250.0g
Preparation of Yeast Extract Solution: Add baker’s yeast to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Filter through a paper filter. Adjust
Nicotinamide adenine dinucleotide ..................0.03g Hematin.............................................................0.03g
Preparation of HTM Supplement: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except HTM supplement, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C. Aseptically add 10.0mL of sterile HTM supplement. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes. Use: For antimicrobial susceptibility testing of Haemophilus influenzae.
Haemophilus Test Medium (HTM Base) Composition per liter: Beef infusion from..........................................300.0g Acid hydrolysate of casein................................17.5g Agar ..................................................................17.0g Yeast extract, selected for low antagonist levels.............................................................5.0g
236
Ham’s F-10 Medium
Starch ..................................................................1.5g Supplement solution ..................................... 10.0mL pH 7.4 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath. Supplement Solution: Composition per 10.0mL: NAD...............................................................15.0mg Hematin..........................................................15.0mg
Preparation of Supplement Solution: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except supplement solution, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C. Aseptially add 10.0mL supplement solution. Mix thouroughly. Pour into sterile Petri dishes.
Use: For the susceptibility testing of Haemophilus influenzae. The medium forms part of the recommended methods of the United States National Committee for Clinical Laboratory Standards (NCCLS). Haemophilus influenzae require complex media for growth. These complex media have aggravated the routine susceptibility testing of Haemophilus influenzae because of antagonism between some essential nutrients and certain antimicrobial agents. This medium overcomes those limitations. The transparency of the medium allows zones of inhibition to be read easily through the bottom of the Petri dish. HTM contains low levels of antimicrobial antagonists, which allows testing of trimethoprim/sulphamethoxazole to be carried out.
Ham’s F-10 Medium
L-Glutamic
acid.................................................0.01g ..........................................................0.01g L-Proline............................................................0.01g L-Serine .............................................................0.01g L-Alanine..........................................................8.9mg Glycine.............................................................7.5mg D-Phenylalanine ...............................................5.0mg L-Methionine ....................................................4.5mg Hypoxanthine...................................................4.1mg L-Threonine ......................................................3.6mg L-Valine ........................................................... 3.5mg L-Isoleucine ......................................................2.6mg L-Tyrosine ........................................................1.8mg Vitamin B12 ......................................................1.4mg Folic acid .........................................................1.3mg Phenol Red.......................................................1.2mg Thiamine·HCl ..................................................1.0mg FeSO4·7H2O ....................................................0.8mg Choline chloride...............................................0.7mg D-Calcium pantothenate ...................................0.7mg Thymidine........................................................0.7mg Niacinamide.....................................................0.6mg L-Tryptophan....................................................0.6mg Isoinositol ........................................................0.5mg Riboflavin ........................................................0.4mg Lipoic acid .......................................................0.2mg Pyridoxine·HCl ................................................0.2mg ZnSO4·7H2O ..................................................0.03mg Biotin .............................................................0.02mg CuSO4·5H2O .....................................................3.0µg pH 7.0 ± 0.2 at 25°C L-Leucine
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
Use: For the growth of Y-1 cell cultures used in the mouse adrenal assay for heat-labile toxin of enterotoxigenic Escherichia coli and Vibrio species.
Composition per liter: NaCl ....................................................................7.4g NaHCO3 ..............................................................1.2g Glucose ...............................................................1.1g NaH2PO4·H2O...................................................0.29g KCl....................................................................0.28g L-Arginine·HCl..................................................0.21g L-Glutamine.......................................................0.15g MgSO4·7H2O ....................................................0.15g Sodium pyruvate ...............................................0.11g KH2PO4 .............................................................0.08g CaCl2·2H2O.......................................................0.04g L-Cystine·2HCl..................................................0.04g L-Histidine·HCl·H2O .........................................0.02g L-Lysine·HCl .....................................................0.02g L-Asparagine-H2O.............................................0.01g L-Aspartic acid ..................................................0.01g
HBT Bilayer Medium (Human Blood Tween Bilayer Medium) Composition per 1062.5mL: Agar ..................................................................13.5g Pancreatic digest of casein................................12.0g Casein/meat peptone.........................................10.0g NaCl....................................................................5.0g Peptic digest of animal tissue .............................5.0g Beef extract.........................................................3.0g Yeast extract........................................................3.0g Cornstarch...........................................................1.0g Human blood, anticoagulated ....................... 25.0mL Colistin solution............................................ 10.0mL Nalidixic acid solution.................................. 10.0mL
Heart Infusion Agar Amphotericin B solution............................... 10.0mL Polysorbate 80 (Tween 80) solution ............... 7.5mL pH 7.3 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Colistin Solution: Composition per liter: Colistin..............................................................0.01g
Preparation of Colistin: Add colistin to distilled/ deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
237
Use: For the selective isolation, cultivation, and differentiation of Gardnerella vaginalis from clinical specimens.
Heart Infusion Agar Composition per liter: Beef heart, infusion from................................500.0g Agar ..................................................................15.0g Tryptose ............................................................10.0g NaCl....................................................................5.0g pH 7.4 ± 0.2 at 25°C
Nalidixic Acid Solution: Composition per liter:
Source: This medium is available as a premixed
Nalidixic acid ....................................................0.02g
Preparation of Medium: Add components to
Preparation of Nalidixic Acid Solution: Add
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
nalidixic acid to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Amphotericin B Solution: Composition per liter: Amphotericin B................................................3.0mg
Preparation of Amphotericin B Solution: Add Amphotericin B to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Tween 80 Solution: Composition per 100.0mL:
powder from BD Diagnostic Systems.
Use: For the isolation and cultivation of a wide variety of fastidious microorganisms. It can also be used as a base for the preparation of blood agar in determining hemolytic reactions. For the cultivation and maintenance of Bacillus anthracis, Bacillus cereus, Bacillus mycoides, Serratia rubidaea, Staphylococcus aureus, Tsatumella ptyseos, and Vibrio vulnificus.
Tween 80......................................................... 1.0mL
Preparation of Tween 80 Solution: Add Tween 80 to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Adjust pH to 7.3. Filter sterilize. Preparation of Medium: Add components, except amphotericin B, Tween 80, and human blood, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Divide the medium into two 500.0mL fractions. Autoclave both flasks of media for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. To one flask, aseptically add 5.0mL of sterile colistin solution, 5.0mL of sterile nalidixic acid solution, 5.0mL of sterile amphotericin B solution, and 3.75mL of Tween 80 solution. Mix thoroughly. Pour into sterile Petri dishes in 7.0mL volumes. Allow agar to harden. To remaining flask aseptically add 5.0mL of sterile colistin solution, 5.0mL of sterile nalidixic acid solution, 5.0mL of sterile amphotericin B solution, 3.75mL of sterile Tween 80 solution, and 25.0mL of sterile human blood. Mix thoroughly. Pour into the same Petri dishes that each contain 7.0mL of the agar medium without blood. The top layer should be approximately 14.0mL per plate.
Heart Infusion Agar Composition per liter: Beef heart, infusion from................................500.0g Agar ..................................................................15.0g Tryptose ............................................................10.0g NaCl....................................................................5.0g Horse blood, sterile defibrinated................... 50.0mL pH 7.4 ± 0.2 at 25°C
Source: This medium without agar is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components, except horse blood, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C. Aseptially add 50.0mL sterile defibrinated horse blood. Mix thouroughly. Pour into sterile Petri dishes.
Use: For the isolation and cultivation of a wide variety of fastidious microorganisms. For the cultivation and maintenance of Bacillus cereus, Staphylococcus aureus, and Vibrio vulnificus, especially for determining hemolytic reactions.
238
Heart Infusion Agar with Glucose
Heart Infusion Agar with Glucose Composition per liter:
add sterile horse serum. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Beef heart, infusion from ................................500.0g Agar ..................................................................15.0g Tryptose ............................................................10.0g NaCl ....................................................................5.0g Glucose ...............................................................1.0g pH 7.4 ± 0.2 at 25°C
Use: For the cultivation and maintenance of Coryne-
Preparation of Medium: Add components to
Beef heart, infusion from................................500.0g Agar ..................................................................15.0g Tryptose ............................................................10.0g NaCl....................................................................5.0g Horse serum, inactivated ............................ 100.0mL pH 7.4 ± 0.2 at 25°C
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of Bacillus species and Pseudomonas species.
Heart Infusion Agar with 0.1% Glucose Composition per liter: Beef heart, infusion from ................................500.0g Agar ..................................................................15.0g Tryptose ............................................................10.0g NaCl ....................................................................5.0g Glucose ...............................................................1.0g pH 7.4 ± 0.2 at 25°C
Source: This medium without glucose is available
bacterium species.
Heart Infusion Agar with Inactivated Horse Serum Composition per liter:
Preparation of Medium: Add components, except horse serum, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile horse serum. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation and maintenance of Corynebacterium species.
Heart Infusion Agar with Inactivated Horse Serum, NaCl, and Penicillin
as a premixed powder from BD Diagnostic Systems.
Composition per liter:
Preparation of Medium: Add components to
Beef heart, infusion from................................500.0g NaCl..................................................................35.0g Agar ..................................................................15.0g Tryptose ............................................................10.0g Horse serum, inactivated ............................ 100.0mL Penicillin solution ......................................... 10.0mL pH 7.4 ± 0.2 at 25°C
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the isolation and cultivation of Bacillus circulans and Pseudomonas spp.
Heart Infusion Agar (pH 7.6) with Inactivated Horse Serum (ATCC Medium 493) Composition per liter: Beef heart, infusion from ................................500.0g Agar ..................................................................15.0g Tryptose ............................................................10.0g NaCl ....................................................................5.0g Horse serum, inactivated............................. 100.0mL pH 7.6 ± 0.2 at 25°C
Preparation of Medium: Add components, except horse serum, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically
Penicillin Solution: Composition per 10.0mL: Penicillin ................................................. 1,000,000U
Preparation of Penicillin Solution: Add penicillin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except penicillin solution and horse serum, to distilled/ deionized water and bring volume to 890.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 10.0mL of sterile penicillin solution and 100.0mL of sterile horse serum. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation and maintenance of Corynebacterium species.
Heart Infusion Broth with Additives for Streptobacillus
Heart Infusion Agar with Rabbit Blood Composition per liter: Beef heart, infusion from ................................500.0g Agar ..................................................................15.0g Tryptose ............................................................10.0g NaCl ....................................................................5.0g Rabbit blood.................................................. 50.0mL pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components, except rabbit blood, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile rabbit blood. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation and maintenance of Neisseria lactamica, Bartonella quintana, Bartonella elizabethae, and Bartonella henselae.
Heart Infusion Broth Composition per liter: Beef heart, infusion from ................................500.0g Tryptose ............................................................10.0g NaCl ....................................................................5.0g pH 7.4 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the isolation and cultivation of a wide variety of fastidious microorganisms.
Heart Infusion Broth (pH 7.5) with Inactivated Human Serum and Yeast Extract (ATCC Medium 245) Composition per liter: Heart infusion broth with yeast extract....... 800.0mL Human serum, inactivated .......................... 200.0mL pH 7.5 ± 0.2 at 25°C
Heart Infusion Broth with Yeast Extract: Composition per liter: Beef heart, infusion from ................................500.0g Tryptose ............................................................10.0g Yeast extract (Oxoid) ..........................................6.3g NaCl ....................................................................5.0g
239
ly. Adjust pH to 7.5. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°.
Source: Heart infusion broth without yeast extract is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: To 800.0mL of sterile cooled heart infusion broth with yeast extract, aseptically add 200.0mL of heat inactivated human serum. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation and maintenance of Corynebacterium pseudotuberculosis and Streptobacillus moniliformis.
Heart Infusion Broth with Additives for Staphylococcus Composition per liter: Beef heart, infusion from................................500.0g NaCl.................................................................30.0 g Tryptose ............................................................10.0g Horse serum, inactivated ............................ 100.0mL Penicillin solution ......................................... 10.0mL Fresh yeast extract solution ............................ 5.0mL pH 7.4 ± 0.2 at 25°C
Penicillin Solution: Composition per 10.0mL: Penicillin ................................................. 1,000,000U
Preparation of Penicillin Solution: Add penicillin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Fresh Yeast Extract Solution: Composition per 100.0mL: Baker’s yeast, live, pressed, starch-free............10.0g
Preparation of Fresh Yeast Extract Solution: Add the live Baker’s yeast to 100.0mL of distilled/ deionized water. Autoclave for 90 min at 15 psi pressure–121°C. Allow to stand. Remove supernatant solution. Adjust pH to 6.6–6.8. Preparation of Medium: Add components—except horse serum, fresh yeast extract solution, and penicillin solution—to distilled/deionized water and bring volume to 800.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile horse serum. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation of Staphylococcus species.
Heart Infusion Broth with Additives for Streptobacillus
Preparation of Heart Infusion Broth with Yeast Extract: Add components to distilled/deion-
Composition per liter:
ized water and bring volume to 1.0L. Mix thorough-
Beef heart, infusion from................................500.0g
240
Heart Infusion Broth with Inactivated Horse Serum and Fresh Yeast Extract
Tryptose ............................................................10.0g Peptone..............................................................10.0g NaCl ....................................................................5.0g Glucose ...............................................................0.5g Horse serum, inactivated............................. 200.0mL pH 7.5 ± 0.2 at 25°C
Sucrose..............................................................40.0g Tryptose ............................................................10.0g NaCl....................................................................5.0g Horse serum, inactivated ............................ 200.0mL Fresh yeast extract solution ........................ 100.0mL pH 7.5 ± 0.2 at 25°C
Preparation of Medium: Add components, ex-
Source: This medium is available as a premixed
cept horse serum, to distilled/deionized water and bring volume to 800.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile horse serum. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation and maintenance of Streptobacillus moniliformis.
Heart Infusion Broth with Inactivated Horse Serum and Fresh Yeast Extract Composition per liter: Beef heart, infusion from ................................500.0g Tryptose ............................................................10.0g NaCl ....................................................................5.0g Horse serum, inactivated............................. 200.0mL Fresh yeast extract solution......................... 100.0mL pH 7.5 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Fresh Yeast Extract Solution: Composition per 100.0mL: Baker’s yeast, live, pressed, starch-free............25.0g
Preparation of Fresh Yeast Extract Solution: Add the live Baker’s yeast to 100.0mL of distilled/ deionized water. Autoclave for 90 min at 15 psi pressure–121°C. Allow to stand. Remove supernatant solution. Adjust pH to 6.6–6.8. Preparation of Medium: Add components, except horse serum and fresh yeast extract solution, to distilled/ deionized water and bring volume to 700.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile horse serum and fresh yeast extract solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation and maintenance of Acholeplasma species, Mycoplasma species, and Streptobacillus species.
Heart Infusion Broth with Inactivated Horse Serum, Fresh Yeast Extract, and Sucrose Composition per liter: Beef heart, infusion from ................................500.0g
powder from BD Diagnostic Systems.
Fresh Yeast Extract Solution: Composition per 100.0mL: Baker’s yeast, live, pressed, starch-free............25.0g
Preparation of Fresh Yeast Extract Solution: Add the live Baker’s yeast to 100.0mL of distilled/ deionized water. Autoclave for 90 min at 15 psi pressure–121°C. Allow to stand. Remove supernatant solution. Adjust pH to 6.6–6.8. Preparation of Medium: Add components, except horse serum and fresh yeast extract solution, to distilled/ deionized water and bring volume to 700.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile horse serum and fresh yeast extract solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation and maintenance of Acholeplasma species, Mycoplasma species, and Streptobacillus species.
Heart Infusion Medium with Fetal Bovine Serum Composition per liter: Beef heart, infusion from................................500.0g Agar ..................................................................15.0g Tryptose ............................................................10.0g NaCl....................................................................5.0g Fetal bovine serum...................................... 100.0mL pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components, except fetal bovine serum, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile fetal bovine serum. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation of Haemophilus ducreyi.
Heart Infusion Tyrosine Agar Composition per liter: Beef heart, infusion from................................500.0g Agar ..................................................................15.0g Tryptose ............................................................10.0g
Helicobacter pylori Selective Medium NaCl ....................................................................5.0g L-Tyrosine............................................................1.0g pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes. Autoclave for 15 min at 15 psi pressure–121°C. Allow tubes to cool in a slanted position.
Use: For the cultivation and differentiation of Bordetella parapertussis based on browning of blood-free medium.
Hektoen Enteric Agar Composition per liter: Agar ..................................................................13.5g Lactose ..............................................................12.0g Peptic digest of animal tissue............................12.0g Sucrose..............................................................12.0g Bile salts..............................................................9.0g NaCl ....................................................................5.0g Na2S2O3 ..............................................................5.0g Yeast extract........................................................3.0g Salicin .................................................................2.0g Ferric ammonium citrate.....................................1.5g Acid Fuchsin .......................................................0.1g Bromthymol Blue ...........................................0.064g pH 7.6 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems and Oxoid Unipath.
Caution: Acid Fuchsin is a potential carcinogen and care must be taken to avoid inhalation of the powdered dye and contact with the skin.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring until components are dissolved. Do not autoclave. Pour into sterile Petri dishes. Allow agar to solidify with the Petri dish covers partially off.
Use: For the isolation and cultivation of Gram-negative enteric microorganisms from a variety of clinical and nonclinical specimens based on lactose or sucrose fermentation and H2S production. For the isolation and differentiation of Salmonella and Shigella. Bacteria that ferment lactose or sucrose appear as yellow to orange colonies. Bacteria that produce H2S appear as colonies with black centers.
Helicobacter pylori Isolation Agar
241
Bitone................................................................10.0g Pancreatic digest of casein..................................5.0g NaCl....................................................................5.0g Peptic digest of animal tissue .............................5.0g Tryptic digest of beef heart.................................3.0g Cornstarch...........................................................1.0g Horse blood, laked ........................................ 35.0mL Antibiotic inhibitor solution ......................... 10.0mL pH 7.3 ± 0.2 at 25°C
Antibiotic Inhibitor Solution: Composition per 10.0mL: Vancomycin ......................................................0.01g Amphotericin B ...............................................5.0mg Cefsulodin........................................................5.0mg Trimethoprim lactate........................................5.0mg
Preparation of Antibiotic Inhibitor Solution: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except horse blood and antibiotic inhibitor solution, to distilled/deionized water and bring volume to 955.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C. Aseptically add sterile horse blood and sterile antibiotic inhibitor solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation and cultivation of Helicobacter pylori from clinical specimens.
Helicobacter pylori Selective Medium Composition per 1080mL: Special peptone.................................................23.0g Agar ..................................................................10.0g NaCl....................................................................5.0g Starch ..................................................................1.0g Horse blood, laked ........................................ 70.0mL Selective supplement solution ...................... 10.0mL pH 7.3 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath.
Horse Blood, Laked: Composition per 100.0mL: Horse blood, fresh....................................... 100.0mL
Preparation of Horse Blood, Laked: Add blood to a sterile polypropylene bottle. Freeze overnight at −20°C. Thaw at 8°C. Refreeze at −20°C. Thaw again at 8°C.
Composition per liter:
Selective Supplement Solution: Composition per 10.0mL:
Agar ..................................................................15.0g
Vancomycin ...................................................10.0mg
242
Hemo ID Quad Plate with Growth Factors
Trimethoprim ...................................................5.0mg Cefsulodin........................................................5.0mg Amphotericin B................................................5.0mg
This enrichment may be replaced by supplement VX from BD Diagnostic Systems.
Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Quadrant Media: Sterilize Brain Heart Infusion Agar by autocalving for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Add additional components as filter sterilized solutions. Mix and distribute as 5.0mL aliquots into quadrants.
Preparation of Medium: Add components, ex-
Use: For the differentiation and presumptive identifica-
cept selective supplement solution and laked horse blood, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C. Aseptially add 10.0mL selective supplement solution and 70.0mL sterile laked horse blood. Mix thouroughly. Pour into sterile Petri dishes.
Hemorrhagic Coli Agar (HC Agar)
Preparation of Selective Supplement Solution:
Use: For the isolation of Helicobacter pylori from clinical specimens. H. pylori forms discrete, translucent and non-coalescent colonies.
Hemo ID Quad Plate with Growth Factors (Hemophilus Identification Quadrant Plate with Growth Factors) Composition per plate: Quadrant I ....................................................... 5.0mL Quadrant II...................................................... 5.0mL Quadrant III..................................................... 5.0mL Quadrant IV .................................................... 5.0mL
Quadrant I: Composition per 5.0mL: Hemin...............................................................0.1mg Brain heart infusion agar................................. 5.0mL
Quadrant II: Composition per 5.0mL: Brain heart infusion agar................................. 5.0mL Supplement solution ..................................... 0.05mL
Quadrant III: Composition per 5.0mL: Hemin...............................................................0.1mg Brain heart infusion agar................................. 5.0mL Supplement solution ..................................... 0.05mL
Quadrant IV: Composition per 5.0mL: Hemin...............................................................0.1mg Brain heart infusion agar................................. 5.0mL Horse blood................................................... 0.25mL Supplement solution ..................................... 0.05mL
Source: The supplement solution (IsoVitaleX enrichment) is available from BD Diagnostic Systems.
tion of Haemophilus species. The Hemo ID Quad Plate is a four-sectored plate, each with a different medium.
Composition per liter: Sorbitol .............................................................20.0g Pancreatic digest of casein................................20.0g Agar ..................................................................15.0g NaCl....................................................................5.0g Bile salts no. 3...................................................1.12g Bromcresol Purple ..........................................0.015g pH 7.2 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes.
Use: For the isolation and cultivation of enterohemorraghic Escherichia coli.
Herellea Agar Composition per liter: Agar ..................................................................16.0g Pancreatic digest of casein................................15.0g Lactose..............................................................10.0g Maltose .............................................................10.0g Enzymatic digest of soybean meal .....................5.0g NaCl....................................................................5.0g Bile salts............................................................1.25g Bromcresol Purple ............................................0.02g pH 6.8 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the isolation, cultivation, and differentiation of Gram-negative nonfermentative and fermentative bacteria. It is especially recommended for the differentiation of Acinetobacter (Herellea) species
Hexamita Medium from Neisseria gonorrhoeae in urethral or vaginal specimens. Fermentative bacteria appear as yellow colonies surrounded by yellow zones. Nonfermentative bacteria, such as Acinetobacter species, appear as pale lavender colonies.
Hershey’s Tris-Buffered Salts Medium Composition per liter: Tris(hydroxymethyl)aminomethane buffer (0.1M solution)..................12.1g NaCl ....................................................................5.4g KCl......................................................................3.0g NH4Cl .................................................................1.1g MgCl2 ..............................................................0.095g KH2PO4 ...........................................................0.087g Na2SO4 ............................................................0.023g CaCl2 ...............................................................0.011g FeCl3 ..............................................................0.16mg Glucose solution ......................................... 100.0mL pH 7.4 ± 0.2 at 25°C
Glucose Solution: Composition per 100.0mL:
243
Tween Solution: Composition per 100.0mL: Tween 80....................................................... 10.0mL
Preparation of Tween Solution: Add Tween 80 to absolute ethanol and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Rice Starch Solution: Composition per 100.0mL: Rice starch ..........................................................5.0g Phosphate buffered saline solution ............. 100.0mL
Phosphate Buffered Saline Solution: Composition per liter: NaCl....................................................................9.0g Na2HPO4·7H2O...............................................0.795g KH2PO4........................................................... 0.114g
Preparation of Phosphate Buffered Saline Solution: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.4. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C.
Glucose ...............................................................2.0g
Preparation of Rice Starch Solution: Heat ster-
Preparation of Glucose Solution: Add glucose
ilize rice starch at 150°C for 2h. Aseptically add 100.0mL of sterile phosphate-buffered saline solution. Mix thoroughly. Use immediately.
to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C.
Preparation of Medium: Add components, except glucose solution, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C. Aseptically add sterile glucose solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation of a variety of heterotrophic microorganisms.
Hexamita Medium Composition per liter: TYGM-9 medium ....................................... 250.0mL Sonneborn's Paramecium medium ............. 750.0mL
TYGM-9 Medium: Composition per liter: NaCl ....................................................................7.5g K2HPO4 ...............................................................2.8g Casein digest .......................................................2.0g Gastric mucin ......................................................2.0g Yeast extract........................................................1.0g KH2PO4 ...............................................................0.4g Bovine serum, heat inactivated..................... 30.0mL Rice starch solution....................................... 30.0mL Tween solution ................................................ 0.5mL pH 7.4 ± 0.2 at 25°C
Preparation of TYGM-9 Medium: Add components, except rice starch solution, Tween solution, and bovine serum, to distilled/deionized water and bring volume to 939.5mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C. Aseptically add 30.0mL of sterile bovine serum, 30.0mL of sterile rice starch solution, and 0.5mL of sterile Tween solution. Mix thoroughly. Aseptically distribute into sterile, screw-capped tubes or flasks.
Sonneborn's Paramecium Medium: Composition per liter: Solution 1........................................................... 1.0L Klebsiella pneumoniae cultured on solution 2 ............................. variable
Solution 1: Composition per liter: Rye grass cerophyll.............................................2.5g Na2HPO4 .............................................................0.5g
Source: Cerophyll can be obtained from Ward's Natural Science Establishment, Inc. Dairy Goat Nutrition distributes Grass Media Culture, which is equivalent. Cereal Leaf Product from Sigma Chemical is similar to cerophyll.
Preparation of Solution 1: Add cerophyll to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boil. Boil for 5
244
HiCrome™ Aureus Agar Base
min. Filter through Whatman #1 filter paper. Add 0.5g of Na2HPO4. Bring volume to 1.0L with distilled/deionized water. Mix thoroughly. Distribute 10.0mL volumes into tubes. Autoclave for 15 min at 15 psi pressure–121°C.
Source: This medium is available from Fluka, Sigma-Aldrich.
Preparation of Medium: Add components, ex-
Agar ..................................................................20.0g Yeast extract........................................................4.0g Glucose .............................................................0.16g
cept egg yolk tellurite emulsion, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C. Aeptically add 50.0mL sterile egg yok tellurite emulsion. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Preparation of Solution 2: Add components to
Use: For the isolation and enumeration of coagulase
Solution 2: Composition per liter:
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute 5.0mL into tubes. Autoclave for 15 min at 15 psi pressure–121°C. Allow tubes to cool in a slanted position.
Preparation of Sonneborn's Paramecium Medium: Inoculate the surface of agar slants of so-
positive Staphylococcus aureus. Coagulase positive S. aureus gives brown black colonies where as S. epidermidis gives yellow, slightly brownish, colonies.
HiCrome Coliform Agar (Coliform Agar, HiCrome)
lution 2 with a culture of Klebsiella pneumoniae. Incubate at 37°C for 24–48h. Scrape cells from the surface of the agar slants and add to 10.0mL of solution 1. Incubate at 30°C for 24h.
Composition per liter:
Preparation of Medium: Aseptically combine 3.0mL of sterile TYGM-9 medium with 9.0mL of Sonneborn's Paramecium medium in 16 × 125mm screw-capped test tubes.
Peptone, special ..................................................3.0g
Use: For the cultivation of Hexamita inflata, Hexamita pusilla, and Trepomonas agilis.
Agar ..................................................................12.0g Sodium chloride..................................................5.0g K2HPO4...............................................................3.0g KH2PO4...............................................................1.7g Sodium pyruvate.................................................1.0g Tryptophan..........................................................1.0g Chromogenic mixture .........................................0.2g
HiCrome™ Aureus Agar Base (Aureus Agar Base) (HiCrome Staphylococcus aureus Agar) (Staphylococcus aureus Agar, HiCrome)
Sodium lauryl sulphate .......................................0.1g
Composition per liter:
Preparation of Medium: Add components to
Agar ..................................................................20.0g Casein enzymic hydrolysate .............................12.0g Sodium pyruvate ...............................................10.0g Beef extract .........................................................6.0g LiCl .....................................................................5.0g Yeast extract........................................................5.0g Pancreatic digest of of gelatin.............................3.0g Chromogenic mixture .........................................2.1g Egg tellurite emulsion................................... 50.0mL pH 7.4 ± 0.2 at 25°C
Caution: Lithium chloride is harmful. Avoid bodily contact and inhalation of vapors. On contact with skin, wash with plenty of water immediately.
Egg Yolk Tellurite Emulsion: Composition per 100.0mL: Sterile saline.................................................. 64.0mL Egg Yolk ....................................................... 30.0mL Sterile potassium tellurite solution, 3.5% ....... 6.0mL
pH 6.8 ± 0.2 at 25°C
Source: This medium is available from Fluka, Sigma-Aldrich. distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Pour into sterile Petri dishes.
Use: For the simultaneous detection of Escherichia coli and total coliforms. Sodium lauryl sulphate inhibits gram-positive organisms. The chromogenic mixture contains two chromogenic substrates as Salmon-GAL and X-glucuronide. The enzyme β-Dgalactosidase produced by coliforms cleaves Salmon-GAL, resulting in the salmon to red coloration of coliform colonies. The enzyme β-D-glucuronidase produced by E. coli, cleaves Xglucuronide. Escherichia coli forms dark blue to violet colored colonies due to cleavage of both Salmon-GAL and X-glucuronide. The addition of tryptophan improves the indole reaction, thereby increasing detection reliability in combination with the two chromogens.
HiCrome ECC Agar
HiCrome Coliform Agar with Novobiocin (Coliform Agar with Novobiocin, HiCrome) Composition per liter: Agar ..................................................................12.0g Sodium chloride..................................................5.0g Peptone, special ..................................................3.0g K2HPO4 ...............................................................3.0g KH2PO4 ...............................................................1.7g Sodium pyruvate .................................................1.0g Tryptophan ..........................................................1.0g Chromogenic mixture .........................................0.2g Sodium lauryl sulphate .......................................0.1g Novobiocin.......................................................5.0mg pH 6.8 ± 0.2 at 25°C
Source: This medium is available from Fluka, Sigma-Aldrich.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Pour into sterile Petri dishes.
Use: For the simultaneous detection of Escherichia coli and total coliforms when high numbers of Grampositive bacteria may be present. Novobiocin and sodium lauryl sulphate inhibit Gram-positive organisms. The chromogenic mixture contains two chromogenic substrates as Salmon-GAL and X-glucuronide. The enzyme β-D-galactosidase produced by coliforms cleaves Salmon-GAL, resulting in the salmon to red coloration of coliform colonies. The enzyme β-D-glucuronidase produced by E. coli, cleaves Xglucuronide. Escherichia coli forms dark blue to violet colored colonies due to cleavage of both Salmon-GAL and X-glucuronide. The addition of tryptophan improves the indole reaction, thereby increasing detection reliability in combination with the two chromogens.
HiCrome E. coli Agar A (E. coli Agar A, HiCrome) Composition per liter: Casein enzymic hydrolysate .............................14.0g Agar ..................................................................12.0g Peptone, special ..................................................5.0g NaCl ....................................................................2.4g Bile salts mixture ................................................1.5g Na2HPO4 .............................................................1.0g NaH2PO4 .............................................................0.6g X-Glucuronide ................................................0.075g pH 7.2 ± 0.2 at 25°C
245
Source: This medium is available from Fluka, Sigma-Aldrich.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 50°C. Pour into sterile Petri dishes.
Use: For the detection and enumeration of Escherichia coli without further confirmation on membrane filter or by indole reagent. The chromogenic agent Xglucuronide used in this medium helps to detect glucuronidase activity. E. coli cells absorb X-glucuronide and the intracellular glucuronidase splits the bond between the chromophore and the glucuronide. The released chromophore gives coloration to the colonies. Bile salts mixture inhibits gram-positive organisms.
HiCrome E. coli Agar B (E. coli Agar B, HiCrome) Composition per liter: Casein enzymic hydrolysate .............................20.0g Agar ..................................................................15.0g Bile salts mixture ................................................1.5g X-Glucuronide ................................................0.075g pH 7.2 ± 0.2 at 25°C
Source: This medium is available from Fluka, Sigma-Aldrich.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Pour into sterile Petri dishes.
Use: For the detection and enumeration of Escherichia coli without further confirmation on membrane filter or by indole reagent. The chromogenic agent X-glucuronide used in this medium helps to detect glucuronidase activity. E. coli cells absorb Xglucuronide and the intracellular glucuronidase splits the bond between the chromophore and the glucuronide. The released chromophore gives coloration to the colonies. Bile salts mixture inhibits gram-positive organisms.
HiCrome ECC Agar (ECC Agar, HiCrome) Composition per liter: Chromogenic mixture .......................................20.3g Agar ..................................................................15.0g Peptone, special ..................................................5.0g NaCl....................................................................5.0g Na2HPO4 .............................................................3.5g
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HiCrome ECC Selective Agar
Yeast extract........................................................3.0g Lactose ................................................................2.5g KH2PO4 ...............................................................1.5g Neutral Red .......................................................0.03g pH 6.8 ± 0.2 at 25°C
Source: This medium is available from Fluka, Sigma-Aldrich.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Pour into sterile Petri dishes.
Use: A differential medium for presumptive identification of E. coli and other coliforms. The chromogenic mixture contains two chromogens as X-glucuronide and Salmon-GAL. X-glucuronide is cleaved by the the enzyme β-glucuronidase produced by E. coli. Salmon-GAL is cleaved by the enzyme galactosidase produced by the majority of coliforms, including E. coli.
HiCrome ECC Selective Agar (ECC Selective Agar, HiCrome) Composition per liter:
of coliform colonies. The enzyme β-D-glucuronidase produced by E. coli, cleaves X-glucuronide. E. coli forms dark blue to violet colored colonies due to cleavage of both Salmon-GAL and X- glucuronide. The addition of tryptophan improves the indole reaction.
HiCrome ECC Selective Agar (ECC Selective Agar, HiCrome) Composition per liter: Agar ..................................................................10.0g Peptone, special ..................................................6.0g Casein enzymic hydrolysate ...............................3.3g NaCl....................................................................2.0g Sodium pyruvate.................................................1.0g Tryptophane ........................................................1.0g Sorbitol ...............................................................1.0g Na2HPO4 .............................................................1.0g NaH2PO4 .............................................................0.6g Tergitol 7...........................................................0.15g Chromogenic mixture .......................................0.43g Cefulodin .........................................................5.0mg pH 6.8 ± 0.2 at 25°C
Source: This medium is available from Fluka, Sig-
Agar ..................................................................10.0g Peptone, special ..................................................6.0g Casein enzymic hydrolysate ...............................3.3g NaCl ....................................................................2.0g Sodium pyruvate .................................................1.0g Tryptophane ........................................................1.0g Sorbitol................................................................1.0g Na2HPO4 .............................................................1.0g NaH2PO4 .............................................................0.6g Tergitol 7 ...........................................................0.15g Chromogenic mixture .......................................0.43g pH 6.8 ± 0.2 at 25°C
ma-Aldrich.
Source: This medium is available from Fluka, Sig-
The cefsulodin inhibits Pseudomonas and Aeromonas species. The chromogenic mixture contains
ma-Aldrich.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly and heat with frequent agitation until components are completely dissolved (approximately 35 min.). Do not autoclave. Cool to 45°–50°C. Pour into sterile Petri dishes. Medium may show haziness.
Use: For detection of Escherichia coli and coliforms. Tergitol inhibits Ggram-positive as well as some Gram-negative bacteria other than coliforms. The chromogenic mixture contains two chromogenic substrates as Salmon-GAL and X-glucuronide. The enzyme β-D-galactosidase produced by coliforms cleaves SalmonGAL, resulting in the salmon to red coloration
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly and heat with frequent agitation until components are completely dissolved (approximately 35 min.). Do not autoclave. Cool to 45°–50°C. Pour into sterile Petri dishes. Medium may show haziness.
Use: For detection of Escherichia coli and coliforms using pour plate or streak plate methods. Tergitol inhibits Gram-positive as well as some Gram-negative bacteria other than coliforms. two chromogenic substrates as Salmon-GAL and X- glucuronide. The enzyme β-D-galactosidase produced by coliforms cleaves SalmonGAL, resulting in the salmon to red coloration of coliform colonies. The enzyme β-D-glucuronidase produced by E. coli, cleaves X-glucuronide. E. coli forms dark blue to violet colored colonies due to cleavage of both Salmon-GAL and X- glucuronide. The addition of Tryptophan improves the indole reaction.
HiCrome ECC Selective Agar (ECC Selective Agar, HiCrome) Composition per liter: Agar ..................................................................10.0g
HiCrome MacConkey-Sorbitol Agar Peptone, special ..................................................6.0g Casein enzymic hydrolysate ...............................3.3g NaCl ....................................................................2.0g Sodium pyruvate .................................................1.0g Tryptophane ........................................................1.0g Sorbitol................................................................1.0g Na2HPO4 .............................................................1.0g NaH2PO4 .............................................................0.6g Chromogenic mixture .......................................0.43g Tergitol 7 ...........................................................0.15g Cefulodin .......................................................10.0mg pH 6.8 ± 0.2 at 25°C
Source: This medium is available from Fluka, Sigma-Aldrich.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly and heat with frequent agitation until components are completely dissolved (approximately 35 min.). Do not autoclave. Cool to 45°–50°C. Pour into sterile Petri dishes. Medium may show haziness.
Use: For detection of Escherichia coli and coliforms using the membrane filter technique. Tergitol inhibits Gram-positive as well as some Gramnegative bacteria other than coliforms. The cefsulodin inhibits Pseudomonas and Aeromonas species. The chromogenic mixture contains two
chromogenic substrates as Salmon-GAL and Xglucuronide. The enzyme β-D-galactosidase produced by coliforms cleaves Salmon-GAL, resulting in the salmon to red coloration of coliform colonies. The enzyme β-D-glucuronidase produced by E. coli, cleaves X-glucuronide. E. coli forms dark blue to violet colored colonies due to cleavage of both Salmon-GAL and X-glucuronide. The addition of tryptophan improves the indole reaction.
HiCrome Enterococci Broth (Enterococci HiCrome Broth) Composition per liter: Peptone, special ................................................10.0g NaCl ....................................................................5.0g Polysorbate 80.....................................................2.0g NaH2PO4 ...........................................................1.25g NaN3 ...................................................................0.3g Chromogenic mixture .......................................0.04g pH 7.5 ± 0.2 at 25°C
Source: This medium is available from Fluka, Sigma-Aldrich.
Caution: Sodium azide is toxic. It also has a tendency to form explosive metal azides with plumbing ma-
247
terials. It is advisable to use enough water to flush off the disposables.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the rapid and easy identification and differentiation of enterococci. It contains a chromogenic substrate which aids in the detection of enterococci.
HiCrome Listeria Agar Base, Modified (Listeria HiCrome Agar Base, Modified) Composition per liter: Peptone, special ................................................23.0g Agar ..................................................................13.0g Rhamnose .........................................................10.0g Chromogenic mixture .......................................5.13g LiCl .....................................................................5.0g Meat extract ........................................................5.0g NaCl....................................................................5.0g Yeast extract........................................................1.0g Phenol Red........................................................0.12g pH 7.3 ± 0.2 at 25°C
Caution: Lithium chloride is harmful. Avoid bodily contact and inhalation of vapors. On contact with skin, wash with plenty of water immediately.
Source: This medium is available from Fluka, Sigma-Aldrich.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Pour into sterile Petri dishes.
Use: A selective and differential agar medium recommended for rapid and direct identification of Listeria species, specifically Listeria monocytogenes.
HiCrome MacConkey-Sorbitol Agar MacConkey-Sorbitol Agar, HiCrome Composition per liter: Casein enzymic hydrolysate .............................17.0g Agar ..................................................................13.5g Sorbitol .............................................................10.0g NaCl....................................................................5.0g Proteose peptone.................................................3.0g Bile salts mixture ................................................1.5g 5-Bromo-4-chloro-3-indolyl-β-D-glucuronide sodium salt....................................................0.1g Neutral Red.......................................................0.03g Crystal Violet ..................................................0.001g pH 7.1 ± 0.3 at 25°C
248
HiCrome MacConkey-Sorbitol Agar with Tellurite-Cefixime Supplement
Source: This medium is available from Fluka, Sig-
Caution: Potassium tellurite is toxic.
ma-Aldrich.
Source: This medium is available from Fluka, Sig-
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Mix to completely dissolve components. Do not autoclave. Cool to 50°C. Pour into sterile Petri dishes.
Use: For the direct isolation and differentiation of E. coli 0157:H7-strains. The medium contains sorbitol instead of lactose. Enteropathogenic strains of Escherichia coli 0157:H7 ferment lactose but does not ferment sorbitol and hence produce colorless colonies. Sorbitol fermenting strains of Escherichia coli produce pink-red colonies. The red color is due to production of acid from sorbitol, absorption of neutral red and a subsequent color change of the dye when pH of the medium falls below 6.8. The chromogenic indicator is added to detect the presence of an enzyme β-D-glucuronidase. Strains of Escherichia coli possessing β-D-glucuronidase appear as blue colored colonies on the medium. Enteropathogenic strains of Escherichia coli 0157 do not possess β-Dglucuronidase activity and thus produce colorless colonies. Escherichia coli fermenting sorbitol and possessing β-D-glucuronidase activity produce purple colored colonies. Most of the gram-positive organisms are inhibited by crystal violet and bile salts.
HiCrome MacConkey-Sorbitol Agar with Tellurite-Cefixime Supplement (MacConkey-Sorbitol Agar with Tellurite-Cefixime Supplement) Composition per 1004mL: Casein enzymic hydrolysate .............................17.0g Agar ..................................................................13.5g Sorbitol..............................................................10.0g NaCl ....................................................................5.0g Proteose peptone .................................................3.0g Bile salts mixture ................................................1.5g 5-Bromo-4-chloro-3-indolyl-β-D-glucuronide sodium salt....................................................0.1g Neutral Red .......................................................0.03g Crystal Violet ..................................................0.001g Tellurite-cefixime supplement ........................ 4.0mL pH 7.1 ± 0.3 at 25°C
Tellurite-Cefixime Supplement: Composition per 4.0mL: K2TeO3 .............................................................5.0mg Cefiximine .......................................................0.1mg
Preparation of Tellurite-Cefixime Supplement: Add components to 4.0mL of distilled/deionized water. Mix thoroughly. Filter sterilize.
ma-Aldrich. Tellurite-cefixime supplement is available from Oxoid.
Preparation of Medium: Add components, except tellurite-cefixime supplement, to distilled/ deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Mix to completely dissolve components. Do not autoclave. Cool to 50°C. Add 4.0mL sterile telluritecefixime supplement. Mix thoroughly. Pour into sterile Petri dishes.
Use: For the direct isolation and differentiation of E. coli 0157:H7-strains. The medium contains sorbitol instead of lactose. Enteropathogenic strains of Escherichia coli 0157:H7 ferment lactose but does not ferment sorbitol and hence produce colorless colonies. Sorbitol fermenting strains of Escherichia coli produce pink-red colonies. The red color is due to production of acid from sorbitol, absorption of neutral red and a subsequent color change of the dye when pH of the medium falls below 6.8. the chromogenic indicator is added to detect the presence of an enzyme β-D-glucuronidase. Strains of Escherichia coli possessing β-D-glucuronidase appear as blue colored colonies on the medium. Enteropathogenic strains of Escherichia coli 0157 do not possess β-Dglucuronidase activity and thus produce colorless colonies. Escherichia coli fermenting sorbitol and possessing β-D-glucuronidase activity produce purple colored colonies. Most of the gram-positive organisms are inhibited by crystal violet and bile salts. Addition of tellurite-cefixime supplement makes the medium selective. Potassium tellurite selects the serogroups 0157 from other E. coli serogroups and inhibits Aeromonas species and Providencia species. Cefixime inhibits Proteus species.
HiCrome M-CP Agar Base (M-CP HiCrome Agar Base) (Membrane Clostridium perfringens HiCrome Agar Base) Composition per liter: Tryptose ............................................................30.0g Yeast extract......................................................20.0g Agar ..................................................................15.0g Sucrose................................................................5.0g L-Cysteine·HCl·H2O ...........................................1.0g MgSO4·7H2O ......................................................0.1g FeCl3·6H2O .......................................................0.09g Indoxyl-β-D-glucoside ......................................0.06g Bromocresol Purple ..........................................0.04g pH 7.6 ± 0.2 at 25°C
HiCrome Rapid Coliform Broth
249
Source: This medium is available from Fluka, Sig-
Preparation of Tellurite Solution: Add compo-
ma-Aldrich.
nents to 10.0mL of distilled/deionized water. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Pour into sterile Petri dishes.
Caution: Potassium tellurite is toxic.
Use: For the detection of Clostridium perfringens.
Preparation of Medium: Add components, exept
HiCrome MS.O157 Agar (MS.O157 Agar HiCrome) Composition per liter: Agar ..................................................................12.0g Peptone, special ................................................10.0g Sorbitol................................................................4.0g Bile salt mixture..................................................1.0g Chromogenic mixture .....................................0.731g pH 6.8 ± 0.2 at 25°C
Source: This medium is available from Fluka, Sigma-Aldrich.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Do not autoclave. Cool to 50°C. Pour into sterile Petri dishes.
Use: For the simultaneous detection of Escherichia coli, Escherichia coli 0157:H7 and coliforms. Escherichia coli 0157:H7 gives colorless colonies because of non-fermentation of sorbitol and absence of β-glucuronidase activity, whereas other strains of Escherichia coli having β-glucuronidase activity and fermenting sorbitol appear as steel blue colored colonies. Some non-Escherichia coli 0157:H7 may have some colony color.
HiCrome MS.O157 Agar with Tellurite (MS.O157 Agar with Tellurite, HiCrome)
Source: This medium is available from Fluka, Sigma-Aldrich. tellurite solution, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Do not autoclave. Cool to 45°C. Aseptically add 0.25mL sterile tellurite solution. Mix thoroughly. Pour into sterile Petri dishes.
Use: For the simultaneous detection of Escherichia coli, Escherichia coli 0157:H7, and coliforms. Escherichia coli 0157:H7 gives colorless colonies because of non-fermentation of sorbitol and absence of β-glucuronidase activity, whereas other strains of Escherichia coli having β-glucuronidase activity and fermenting sorbitol appear as steel blue colored colonies. Addition of tellurite makes the medium much more specific and selective.
HiCrome Rapid Coliform Broth (Coliform Rapid HiCrome Broth) (Rapid Coliform HiCrome Broth) Composition per liter: Peptone, special ..................................................5.0g NaCl....................................................................5.0g Na2HPO4 .............................................................2.7g KH2PO4...............................................................2.0g Sorbitol ...............................................................1.0g Sodium lauryl sulfate..........................................0.1g IPTG....................................................................0.1g Chromogenic substrate .....................................0.08g Fluorogenic substrate........................................0.05g pH 6.8 ± 0.3 at 25°C
Composition 1000.25mL:
Source: This medium is available from Fluka, Sig-
Agar ..................................................................12.0g Peptone, special ................................................10.0g Sorbitol................................................................4.0g Bile salt mixture..................................................1.0g Chromogenic mixture .....................................0.731g Tellurite solution ........................................... 0.25mL pH 6.8 ± 0.2 at 25°C
ma-Aldrich.
Tellurite Solution: Composition per 10.0mL:
ichia coli and coliforms on the basics of enzyme substrate reaction from water samples, using a combination of chromogenic and fluorogenic substrate.
K2TeO3 ................................................................0.1g
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Pour into sterile Petri dishes.
Use: For the detection and conformation of Escher-
250
HiCrome Rapid Enterococci Agar
HiCrome Rapid Enterococci Agar (Enterococci Rapid HiCrome Agar) (Rapid Enterococci HiCrome Agar) Composition per liter: Agar ..................................................................15.0g Peptone special .................................................10.0g NaCl ....................................................................5.0g Polysorbate 80.....................................................2.0g Na2HPO4 ...........................................................1.25g NaN3 ...................................................................0.3g Chromogenic mixture .......................................0.06g pH 7.5 ± 0.2 at 25°C
colorless colonies. The characteristic light purple and blue color is due to the chromogenic mixture. Chro-
mogenic medium for detecting and identifying Enterobacteria, proteus species, and other Gram-positive organisms.
HiCrome Salmonella Chromogen Agar (Salmonella Chromogen Agar, HiCrome) (Rambach Equivalent Agar) Composition per liter:
ma-Aldrich.
Agar ..................................................................15.0g Peptic digest of animal tissue .............................5.0g NaCl....................................................................5.0g Yeast extract........................................................2.0g Meat extract ........................................................1.0g Na-deoxycholate .................................................1.0g Chromogenic mixture .......................................1 vial pH 7.3 ± 0.2 at 25°C
Preparation of Medium: Add components to
Source: This medium is available from Fluka, Sig-
Caution: Sodium azide is toxic. It also has a tendency to form explosive metal azides with plumbing materials. It is advisable to use enough water to flush off the disposables.
Source: This medium is available from Fluka, Sig-
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Pour into sterile Petri dishes.
Use: For the rapid and easy identification and differentiation of enterococci. It contains a chromogenic substrate, which aids in the detection of enterococci, especially from water samples.
HiCrome Salmonella Agar (Salmonella Agar, HiCrome) Composition per liter: Agar ..................................................................13.0g Peptic digest of animal tissue..............................6.0g Chromogenic mixture .........................................5.4g Yeast extract........................................................2.5g Chromogenic mix ...............................................1.5g Bile salt mixture..................................................1.0g pH 7.7 ± 0.2 at 25°C
Source: This medium is available from Fluka, Sigma-Aldrich.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Mix to completely dissolve components. Do not autoclave. Cool to 50°C. Pour into sterile Petri dishes.
Use: A selective chromgenic medium used for the isolation and differentiation of Salmonella species from coliforms. E. coli and Salmonella are easily distinguishable due to the colony characteristics. Salmonella give light purple colonies with a halo. E. coli has a characteristic blue color. Other organisms give
ma-Aldrich.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Mix to completely dissolve components. Do not autoclave. Mix and boil in 5 minute sequences for 35-40 min. Cool to 50°C. Shake gently for 3035 min. Pour into sterile Petri dishes.
Use: A selective medium used for the detectgion of Salmonella species. This medium exploits a novel phenotypic characteristic of Salmonella spp.: the formation of acid from propylene glycol. This characteristic may be used in combination with a chromogenic indicator of β-galactosidase to differentiate Salmonella spp. from Proteus spp. and the other members of the Enterobacteriaceae. Desoxycholate is included in the plate medium as an inhibitor of gram-positive organisms. Non-typhi Salmonella spp. yield distinct, bright red colonies on this medium, allowing facilitated identification and unambiguous differentiation from Proteus spp. Coliforms produce blue-green to blue-violet colonies. Other Enterobacteriaceae and Gram-negative bacteria such as Proteus, Shigella, Pseudomonas, Salmonella typhi, and S. paratyphi A form colorless or yellow colonies.
HiCrome UTI Agar, Modified (UTI Agar, Modified HiCrome) Composition per liter: Peptic digest of animal tissue .............................8.0g Agar ..................................................................15.0g Chromogenic mixture .....................................12.44g
Histoplasma capsulatum Agar Beef extract .........................................................4.0g Casein enzymatic hydrolysate ............................4.0g pH: 7.2 ± 0.2 at 25°C
Source: This medium is available from Fluka, Sigma-Aldrich.
Preparation of Medium: Add components to
Preparation of Solution 2: Add 1.0mL of concentrated HCl to 100.0mL of distilled water in a 1.0L volumetric flask. Dissolve each component completely in the sequence given. Bring volume to 1.0L with distilled/deionized water. Store at 5°C. Discard if red color or red precipitate appears.
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Mix to completely dissolve components. Do not autoclave. Cool to 50°C. Pour into sterile Petri dishes.
Solution 3: Composition per 100.0mL:
Use: A chromgenic medium used for detecting and identifying Enterobacteria, Proteus species, and other bacteria involved in urinary tract infections.
Solution 4: Composition per liter:
Histoplasma capsulatum Agar Composition per liter: Agar ..................................................................12.5g Glucose .............................................................10.0g Citric acid..........................................................10.0g Potato starch........................................................2.0g α-Ketoglutaric acid .............................................1.0g L-Cystine·HCl·H2O .............................................1.0g Glutathione, reduced...........................................0.5g L-Asparagine .......................................................0.1g L-Tryptophan .....................................................0.02g Solution 1.................................................... 250.0mL Solution 3...................................................... 40.0mL Solution 2...................................................... 10.0mL Solution 4...................................................... 10.0mL Solution 8...................................................... 10.0mL Solution 5........................................................ 1.0mL Solution 6........................................................ 0.1mL Solution 7........................................................ 0.1mL pH 6.5 ± 0.2 at 25°C
Solution 1: Composition per liter: KH2PO4 ...............................................................8.0g (NH4)2SO4...........................................................8.0g MgSO4·7H2O ....................................................0.86g CaCl2, anhydrous ..............................................0.08g ZnSO4·7H2O .....................................................0.05g
Preparation of Solution 1: Add components to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Bring volume to 1.0L with distilled/deionized water. Store at 5°C.
Solution 2: Composition per liter: FeSO4·7H2O........................................................5.7g MnCl2·6H2O .......................................................0.8g NaMoO4·2H2O..................................................0.15g HCl, concentrated ........................................... 1.0mL
251
Casein, acid-hydrolyzed, vitamin-free..............10.0g
Preparation of Solution 3: Add casein to distilled/deionized water and bring volume to 100.0mL.
Calcium pantothenate .........................................0.2g Inositol ................................................................0.2g Riboflavin ...........................................................0.2g Thiamine·HCl .....................................................0.2g Nicotinamide.......................................................0.1g Biotin ................................................................0.01g
Preparation of Solution 4: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Store at −20°C.
Solution 5: Composition per 100.0mL: Hemin .................................................................0.2g NH4OH, concentrated ..................................... 0.3mL
Preparation of Solution 5: Add hemin to approximately 30.0mL of distilled/deionized water. Add NH4OH. Mix thoroughly until dissolved. Bring volume to 100.0mL with distilled/deionized water. Store at 5° C.
Solution 6: Composition per 10.0mL: DL-Thioctic
acid ................................................0.01g Ethanol (95% solution) ................................. 10.0mL
Preparation of Solution 6: Add DL-thioctic acid to 10.0mL of ethanol. Mix thoroughly. Store at − 20°C.
Solution 7: Composition per 10.0mL: Coenzyme A .....................................................0.01g Na2S·5H2O (0.05% solution) .......................... 0.2mL
Preparation of Solution 7: Prepare Na2S·5H2O
solution in freshly boiled distilled/deionized water. Add coenzyme A to 9.8mL of distilled/deionized water. Mix thoroughly. Add freshly prepared Na2S·5H2O solution. Mix thoroughly. Store the solution at −20°C.
Solution 8: Composition per 100.0mL: Oleic acid ............................................................0.1g
252
Histoplasma capsulatum Agar
Preparation of Solution 8: Add oleic acid to 50.0mL of distilled/deionized water. Adjust pH to 9.0 with NaOH. Gently heat until dissolved. Bring volume to 100.0mL with distilled/deionized water. Store at 5°C.
Preparation of Medium: Add components—except agar, potato starch, and solution 8—to distilled/ deionized water and bring volume to 400.0mL. Mix thoroughly. Adjust pH to 6.5 with 20% KOH solution. Filter sterilize. In a separate flask, add potato starch to 50.0mL of distilled/deionized water. Add the starch solution to 450.0mL of boiling distilled/ deionized water. Add 10.0mL of solution 8 and the agar. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 70°C. Aseptically combine the two sterile solutions. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation and maintenance of Histoplasma capsulatum in the yeast phase. For the cultivation of Histoplasma duboisii, Blastomyces dermatitidis, and Sprotrichum schenckii.
Histoplasma capsulatum Agar Composition per liter: Agar ..................................................................15.0g Glucose .............................................................10.0g Potato starch........................................................2.0g α-Ketoglutaric acid .............................................1.0g L-Cystine·HCl·H2O .............................................1.0g Glutathione, reduced...........................................0.5g L-Asparagine .......................................................0.1g L-Tryptophan .....................................................0.02g Solution 1.................................................... 250.0mL Solution 3...................................................... 40.0mL Solution 2...................................................... 10.0mL Solution 4...................................................... 10.0mL Solution 8...................................................... 10.0mL Solution 5........................................................ 1.0mL Solution 6........................................................ 0.1mL Solution 7........................................................ 0.1mL pH 6.5 ± 0.2 at 25°C
Solution 1: Composition per liter:
Solution 2: Composition per liter: FeSO4·7H2O........................................................5.7g MnCl2·6H2O .......................................................0.8g NaMoO4·2H2O..................................................0.15g HCl, concentrated ........................................... 1.0mL
Preparation of Solution 2: Add the 1.0mL of concentrated HCl to 100.0mL of distilled water in a 1.0L volumetric flask. Dissolve each component completely in the sequence given. Bring volume to 1.0L with distilled/deionized water. Store at 5°C. Discard if red color or red precipitate appears. Solution 3: Composition per 100.0mL: Casein, acid-hydrolyzed, vitamin-free..............10.0g
Preparation of Solution 3: Add casein to distilled/deionized water and bring volume to 100.0mL. Do not use enzymatically digested casein.
Solution 4: Composition per liter: Calcium pantothenate .........................................0.2g Inositol ................................................................0.2g Riboflavin ...........................................................0.2g Thiamine·HCl .....................................................0.2g Nicotinamide.......................................................0.1g Biotin ................................................................0.01g
Preparation of Solution 4: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Store at −20°C.
Solution 5: Composition per 100.0mL: Hemin .................................................................0.2g NH4OH, concentrated ..................................... 0.3mL
Preparation of Solution 5: Add hemin to approximately 30.0mL of distilled/deionized water. Add NH4OH. Mix thoroughly until dissolved. Bring volume to 100.0mL with distilled/deionized water. Store at 5°C.
Solution 6: Composition per 10.0mL: DL-Thioctic
acid ................................................0.01g Ethanol (95% solution) ................................. 10.0mL
Preparation of Solution 6: Add DL-thioctic acid
KH2PO4 ...............................................................8.0g (NH4)2SO4...........................................................8.0g MgSO4·7H2O ....................................................0.86g CaCl2, anhydrous ..............................................0.08g
to 10.0mL of ethanol. Mix thoroughly. Store solution at −20°C.
Preparation of Solution 1: Add components to
Coenzyme A .....................................................0.01g Na2S·5H2O (0.05% solution) .......................... 0.2mL
distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Bring volume to 1.0L with distilled/deionized water. Store at 5°C.
Solution 7: Composition per 10.0mL:
Preparation of Solution 7: Prepare Na2S·5H2O
solution in freshly boiled distilled/deionized water.
Histoplasma capsulatum Broth
253
Add coenzyme A to 9.8mL of distilled/deionized water. Mix thoroughly. Add freshly prepared Na2S·5H2O solution. Mix thoroughly. Store the solution at −20°C.
Preparation of Solution 1: Add components to
Solution 8: Composition per 100.0mL:
Solution 2: Composition per liter:
Oleic acid ............................................................0.1g
Preparation of Solution 8: Add oleic acid to 50.0mL of distilled/deionized water. Adjust pH to 9.0 with NaOH. Gently heat until dissolved. Bring volume to 100.0mL with distilled/deionized water. Store at 5°C.
Preparation of Medium: Add components—except agar, potato starch, and solution 8—to distilled/ deionized water and bring volume to 400.0mL. Mix thoroughly. Adjust pH to 6.5 with 20% KOH solution. Filter sterilize. In a separate flask, add potato starch to 50.0mL of distilled/deionized water. Add the starch solution to 450.0mL of boiling distilled/ deionized water. Add 10.0mL of solution 8 and the agar. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 70°C. Aseptically combine the two sterile solutions. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation and maintenance of Histoplasma capsulatum in the mycelial phase.
Histoplasma capsulatum Broth Composition per liter: Glucose .............................................................10.0g Citric acid..........................................................10.0g α-Ketoglutaric acid .............................................1.0g L-Cystine·HCl·H2O .............................................1.0g Potato starch........................................................0.5g Glutathione, reduced...........................................0.5g L-Asparagine .......................................................0.1g L-Tryptophan .....................................................0.02g Solution 1.................................................... 250.0mL Solution 3...................................................... 40.0mL Solution 2...................................................... 10.0mL Solution 4...................................................... 10.0mL Solution 5........................................................ 1.0mL Solution 8........................................................ 1.0mL Solution 6........................................................ 0.1mL Solution 7........................................................ 0.1mL pH 6.5 ± 0.2 at 25°C
Solution 1: Composition per liter: KH2PO4 ...............................................................8.0g (NH4)2SO4...........................................................8.0g MgSO4·7H2O ....................................................0.86g CaCl2, anhydrous ..............................................0.08g ZnSO4·7H2O .....................................................0.05g
distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Bring volume to 1.0L with distilled/deionized water. Store at 5°C.
FeSO4·7H2O........................................................5.7g MnCl2·6H2O .......................................................0.8g NaMoO4·2H2O..................................................0.15g HCl, concentrated ........................................... 1.0mL
Preparation of Solution 2: Add 1.0mL of concentrated HCl to 100.0mL of distilled water in a 1.0L volumetric flask. Dissolve each component completely in the sequence given. Bring volume to 1.0L with distilled/deionized water. Store at 5°C. Discard if red color or red precipitate appears.
Solution 3: Composition per 100.0mL: Casein, acid-hydrolyzed, vitamin-free..............10.0g
Preparation of Solution 3: Add casein to distilled/deionized water and bring volume to 100.0mL. Do not use enzymatically digested casein.
Solution 4: Composition per liter: Calcium pantothenate .........................................0.2g Inositol ................................................................0.2g Riboflavin ...........................................................0.2g Thiamine·HCl .....................................................0.2g Nicotinamide.......................................................0.1g Biotin ................................................................0.01g
Preparation of Solution 4: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Store at −20°C.
Solution 5: Composition per 100.0mL: Hemin .................................................................0.2g NH4OH, concentrated ..................................... 0.3mL
Preparation of Solution 5: Add hemin to approximately 30.0mL of distilled/deionized water. Add NH4OH. Mix thoroughly until dissolved. Bring volume to 100.0mL with distilled/deionized water. Store at 5°C.
Solution 6: Composition per 10.0mL: DL-Thioctic
acid ................................................0.01g Ethanol (95% solution) ................................. 10.0mL
Preparation of Solution 6: Add DL-thioctic acid to 10.0mL of ethanol. Mix thoroughly. Store solution at −20°C.
254
HL Agar
Solution 7: Composition per 10.0mL:
boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C.
Coenzyme A .....................................................0.01g Na2S·5H2O (0.05% solution) .......................... 0.2mL
Columbia Blood Top Agar: Composition per liter:
Preparation of Solution 7: Prepare Na2S·5H2O
Agar ..................................................................13.5g Pancreatic digest of casein................................12.0g NaCl....................................................................5.0g Peptic digest of animal tissue .............................5.0g Beef extract.........................................................3.0g Yeast extract........................................................3.0g Cornstarch...........................................................1.0g Horse blood, defibrinated ............................. 50.0mL
solution in freshly boiled distilled/deionized water. Add coenzyme A to 9.8mL of distilled/deionized water. Mix thoroughly. Add freshly prepared Na2S·5H2O solution. Mix thoroughly. Store the solution at −20°C.
Solution 8: Composition per 100.0mL: Oleic acid ............................................................0.1g
Preparation of Columbia Blood Top Agar:
50.0mL of distilled/deionized water. Adjust pH to 9.0 with NaOH. Gently heat until dissolved. Bring volume to 100.0mL with distilled/deionized water. Store at 5°C.
Add components, except horse blood, to distilled/ deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile horse blood. Mix thoroughly.
Preparation of Medium: Add components—ex-
Preparation of Medium: Pour cooled, sterile Co-
Preparation of Solution 8: Add oleic acid to
cept potato starch and solution 8—to distilled/deionized water and bring volume to 400.0mL. Mix thoroughly. Adjust pH to 6.5 with 20% KOH solution. Filter sterilize. In a separate flask, add potato starch to 50.0mL of distilled/deionized water. Add the starch solution to 450.0mL of boiling distilled/ deionized water. Add 1.0mL of solution 8. Mix thoroughly. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 70°C. Aseptically combine the two sterile solutions. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation of Histoplasma capsulatum in the yeast phase. For the cultivation of Histoplasma duboisii, Blastomyces dermatitidis, and Sprotrichum schenckii.
HL Agar Composition per plate: Columbia agar base....................................... 10.0mL Columbia blood top agar................................. 5.0mL pH 7.3 ± 0.2 at 25°C
Columbia Agar Base: Composition per liter: Agar ..................................................................13.5g Pancreatic digest of casein................................12.0g NaCl ....................................................................5.0g Peptic digest of animal tissue..............................5.0g Beef extract .........................................................3.0g Yeast extract........................................................3.0g Cornstarch...........................................................1.0g
lumbia agar base into sterile Petri dishes in 10.0mL volumes. Allow agar to solidify. Pour 5.0mL of cooled, sterile Columbia blood top agar over Columbia agar base that has solidified but is still warm.
Use: For the cultivation of Listeria monocytogenes.
HO-LE Trace Elements Solution Composition per liter: H3BO3 ...............................................................2.85g MnCl2·4H2O .......................................................1.8g Sodium tartrate..................................................1.77g FeSO4 ................................................................1.36g CoCl2·6H2O ......................................................0.04g CuCl2·2H2O ....................................................0.026g Na2MoO4·2H2O ..............................................0.025g ZnCl2 ...............................................................0.021g
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For use as an enrichment to other media that require trace minerals.
Horse Blood Agar Composition per liter:
Preparation of Columbia Agar Base: Add
Beef heart, infusion from................................500.0g Agar ..................................................................15.0g Tryptose ............................................................10.0g NaCl....................................................................5.0g Horse blood, defibrinated ............................. 50.0mL pH 6.8 ± 0.2 at 25°C
components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat until
cept horse blood, to distilled/deionized water and
Preparation of Medium: Add components, ex-
Hoyle Medium Base bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile horse blood. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation and maintenance of Yersinia pseudotuberculosis.
Horse Serum Agar Composition per liter: Agar ..................................................................15.0g Pancreatic digest of gelatin .................................5.0g Beef extract .........................................................3.0g Horse serum ................................................ 200.0mL pH 6.8 ± 0.2 at 25°C
255
Horse blood, laked ........................................ 50.0mL Tellurite solution ........................................... 10.0mL pH 7.8 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath.
Horse Blood, Laked: Composition per 50.0mL: Horse blood, fresh......................................... 50.0mL
Preparation of Horse Blood, Laked: Add blood to a sterile polypropylene bottle. Freeze overnight at −20°C. Thaw at 8°C. Refreeze at −20°C. Thaw again at 8°C. Tellurite Solution: Composition per 100.0mL:
Preparation of Medium: Add components, ex-
K2TeO3 ................................................................3.5g
cept horse serum, to distilled/deionized water and bring volume to 800.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile horse serum. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Preparation of Tellurite Solution: Add K2TeO3
Use: For the cultivation and maintenance of
cept laked horse blood and tellurite solution, to distilled/deionized water and bring volume to 1.0L Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C. Aseptically add 50.0mL sterile laked horse blood and 10.0mL sterile tellurite solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Pseudomonas aeruginosa and Streptobacillus moniliformis.
Horse Serum Broth Composition per liter: Pancreatic digest of gelatin .................................5.0g Beef extract .........................................................3.0g Horse serum ................................................ 200.0mL pH 6.8 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components, except horse serum, to distilled/deionized water and bring volume to 800.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile horse serum. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation and maintenance of Pseudomonas aeruginosa and Streptobacillus moniliformis.
Hoyle Medium Composition per 1060mL: Agar ..................................................................15.0g Lab-Lemco powder...........................................10.0g Peptone..............................................................10.0g NaCl ....................................................................5.0g
to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Caution: Potassium tellurite is toxic. Preparation of Medium: Add components, ex-
Use: For the isolation and differentiation of Corynebacterium diphtheriae strains. This meidum permits very rapid growth of all types of Corynebacterium diphtheriae, so that diagnosis is possible after 18h incubation.
Hoyle Medium Base Composition per liter: Agar ..................................................................15.0g Beef extract.......................................................10.0g Peptone .............................................................10.0g NaCl....................................................................5.0g Blood, laked.................................................. 50.0mL Tellurite solution ........................................... 10.0mL pH 7.8 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath.
Tellurite Solution: Composition per 100.0mL: K2TeO3 ................................................................3.5g
Caution: Potassium tellurite is toxic.
256
HR Antifungal Assay Medium Buffered with MOPS
Preparation of Tellurite Solution: Add K2TeO3
to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Biotin ................................................................2.0µg Folic acid ..........................................................2.0µg pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Add components, ex-
Preparation of Medium: Add components, ex-
cept laked blood, to distilled/deionized water and bring volume to 940.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile components. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation and differentiation of Corynebacterium diphtheriae.
HR Antifungal Assay Medium Buffered with MOPS Composition per liter: MOPS (3-N-Morpholinopropanesulfonic acid) buffer.....................34.53g Glucose .............................................................10.0g (NH4)2SO4...........................................................2.5g KH2PO4 ...............................................................1.0g NaHCO3 ..............................................................1.0g Glutamine..........................................................0.58g MgSO4·7H2O ......................................................0.5g CaCl2·2H2O.........................................................0.1g NaCl ....................................................................0.1g L-Lysine.............................................................0.07g L-Isoleucine .......................................................0.05g L-Leucine...........................................................0.05g L-Threonine .......................................................0.05g L-Valine .............................................................0.05g L-Arginine .........................................................0.04g L-Histidine.........................................................0.02g L-Methionine .....................................................0.01g L-Tryptophan ....................................................8.2mg DL-Methionine..................................................2.0mg DL-Tryptophan..................................................2.0mg Inositol .............................................................2.0mg L-Histidine·HCl ................................................1.0mg H3BO3 ..............................................................0.5mg Calciun pantothenate........................................0.4mg MnSO4·H2O .....................................................0.4mg Niacin...............................................................0.4mg Pyridoxine........................................................0.4mg Thiamine·HCl ..................................................0.4mg ZnSO4·7H2O ....................................................0.4mg p-Aminobenzoic acid.......................................0.2mg FeCl3 ................................................................0.2mg Riboflavin ........................................................0.2mg Na2MoO3 .........................................................0.2mg KI .....................................................................0.1mg CuSO4·5H2O ..................................................0.04mg
cept NaHCO3 and MOPS buffer, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Add NaHCO3 and MOPS buffer. Mix thoroughly. Adjust pH to 7.0. Bring volume to 1.0L with distilled/deionized water. Filter sterilize.
Use: For testing the effectiveness of antifungal agents against clinical fungal isolates using the broth dilution susceptibility testing method.
Hugh-Leifson’s Glucose Broth Composition per liter: NaCl..................................................................30.0g Glucose .............................................................10.0g Agar ....................................................................3.0g Peptone ...............................................................2.0g Yeast extract........................................................0.5g Bromcresol Purple ..........................................0.015g pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Adjust pH to 7.4. Distibute into tubes or flasks. Autoclave for 15 min at 15 psi pressure– 121°C.
Use: For the cultivation and differentiation of bacteria based on their ability to ferment glucose. Bacteria that ferment glucose turn the medium yellow.
Hydroxybenzoate Agar Composition per 1001.0mL: Solution A................................................... 490.0mL Solution D................................................... 500.0mL Solution B ..................................................... 10.0mL Solution C ....................................................... 1.0mL pH 7.0 ± 0.2 at 25°C
Solution A: Composition per 490.0mL: 4-Hydroxybenzoic acid.......................................3.0g (NH4)2SO4 ..........................................................3.0g NaCl....................................................................2.5g K2HPO4...............................................................1.6g Yeast extract........................................................0.5g
Preparation of Solution A: Add components to distilled/deionized water and bring volume to 490.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C.
Imidazole Utilization Medium Solution B: Composition per 10.0mL: MgSO4·7H2O ....................................................0.27g
Preparation of Solution B: Add MgSO4·7H2O to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Solution C: Composition per 1.0mL: Fe(NH4)2(SO4)2·6H2O ......................................0.05g
Preparation of Solution C: Add component to distilled/deionized water and bring volume to 1.0mL. Mix thoroughly. Filter sterilize. Prepare solution immediately before adding to solutions A and B.
Solution D: Composition per 500.0mL:
257
Preparation of Solution B: Add MgSO4·7H2O to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Solution C: Composition per 1.0mL: Fe(NH4)2(SO4)2·6H2O ......................................0.05g
Preparation of Solution C: Add component to distilled/deionized water and bring volume to 1.0mL. Mix thoroughly. Filter sterilize. Prepare solution immediately before adding to solutions A and B.
Preparation of Medium: Aseptically combine cooled sterile solution A and cooled sterile solution B. Immediately add 1.0mL of freshly prepared sterile solution C. Adjust pH to 7.0 with 6N NaOH. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Agar ..................................................................14.0g
Use: For the cultivation and maintenance of Coma-
Preparation of Solution D: Add agar to distilled/
monas testosteroni.
deionized water and bring volume to 500.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C.
Preparation of Medium: Aseptically combine cooled sterile solution A, cooled sterile solution B, and cooled sterile solution D. Immediately add 1.0mL of freshly prepared sterile solution C. Adjust pH to 7.0 with 6N NaOH. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes. Use: For the cultivation and maintenance of Comamonas testosteroni.
Hydroxybenzoate Broth
Imidazole Utilization Medium Composition per liter: Imidazole ............................................................5.0g KH2PO4...............................................................0.5g MgSO4·7H2O ......................................................0.5g CaCl2 ................................................................3.0mg FeSO4·7H2O.....................................................3.0mg Molybdenum solution..................................... 1.0mL Trace elements solution .................................. 1.0mL pH 6.0 ± 0.2 at 25°C
Molybdenum Solution: Composition per 18.0mL:
Composition per 1001.0mL:
Na2MoO4·2H2O ...............................................0.5mg
Solution A ................................................... 990.0mL Solution B ..................................................... 10.0mL Solution C ....................................................... 1.0mL pH 7.0 ± 0.2 at 25°C
Preparation of Molybdenum Solution: Add components to distilled/deionized water and bring volume to 18.0mL. Mix thoroughly. Filter sterilize.
Solution A: Composition per 990.0mL: 4-Hydroxybenzoic acid.......................................3.0g (NH4)2SO4...........................................................3.0g NaCl ....................................................................2.5g K2HPO4 ...............................................................1.6g Yeast extract........................................................0.5g
Preparation of Solution A: Add components to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C.
Solution B: Composition per 10.0mL: MgSO4·7H2O ....................................................0.27g
Trace Elements Solution: Composition per 18.0mL: H3BO3 ............................................................11.0mg MnCl2·4H2O ....................................................7.0mg Al2(SO4)3·18 H2O ..........................................1.94mg Co(NO3)2·6H2O ...............................................1.0mg CuSO4·5H2O ....................................................1.0mg NiSO4·6H2O.....................................................1.0mg ZnSO4·H2O ....................................................0.62mg KBr ..................................................................0.5mg KI .....................................................................0.5mg LiCl ..................................................................0.5mg SnCl2·2H2O......................................................0.5mg
Preparation of Trace Elements Solution: Add components to distilled/deionized water and bring volume to 18.0mL. Mix thoroughly. Filter sterilize.
258
Indole Medium
Preparation of Medium: Add components, ex-
Preparation of Medium: Add components to
cept molybdenum solution and trace elements solution, to distilled/deionized water and bring volume to 998.0mL. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 25°C. Aseptically add 1.0mL of molybdenum solution and 1.0mL of trace elements solution. Mix thoroughly. Adjust pH to 6.0 with phosphoric acid. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling with frequent agitation. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure– 121°C.
Use: For the cultivation and maintenance of Pseudomonas species.
Use: For the identification of microorganisms by means of the nitrate reduction and indole tests.
Infection Medium (IM) Composition per 100.0mL:
Indole Medium Composition per 200.0mL: K2HPO4 .............................................................3.13g L-Tryptophan .......................................................1.0g NaCl ....................................................................1.0g KH2PO4.............................................................0.27g pH 7.2 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 200.0mL. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure– 121°C.
Use: For the differentiation of microorganisms by means of indole production from the tryptophan test.
Indole Medium Composition per liter: Pancreatic digest of casein................................20.0g pH 7.3 ± 0.2 at 25°C
Preparation of Medium: Add pancreatic digest
Pancreatic digest of gelatin...............................0.05g Bile salts no. 3...................................................0.05g Brain heart, solids from infusion ......................0.02g Peptic digest of animal tissue ...........................0.02g NaCl................................................................0.017g Glucose .............................................................0.01g Na2HPO4 ..........................................................8.0mg Earle’s balanced salts solution ...................... 80.0mL Fetal bovine serum, heat inactivated (2 hr at 55°C).......................................... 20.0mL pH 7.4 ± 0.2 at 25°C
Earle’s Balanced Salts Solution: Composition per liter: NaCl....................................................................6.8g NaHCO3 ..............................................................2.2g Glucose ...............................................................1.0g KCl......................................................................0.4g CaCl2·2H2O ....................................................0.265g MgSO4·7H2O ......................................................0.2g NaH2PO4·H2O...................................................0.14g
Preparation of Earle’s Balanced Salts Solution: Add components to distilled/deionized water
of casein to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure– 121°C.
and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
Use: For the differentiation of microorganisms by
Use: For the screening of Escherichia coli for patho-
means of the indole test.
Indole Nitrite Medium (Trypticase Nitrate Broth) Composition per liter: Pancreatic digest of casein................................20.0g Na2HPO4 .............................................................2.0g Agar ....................................................................1.0g Glucose ...............................................................1.0g KNO3 ..................................................................1.0g pH 7.2 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Combine components. Mix thoroughly. Filter sterilize. Store at 4°–10°C. genicity using the HeLa cell test for invasiveness.
Infusion Broth Composition per liter: Pancreatic digest of casein................................13.0g NaCl....................................................................5.0g Yeast extract........................................................5.0g Heart muscle, solids from infusion.....................2.0g pH 7.4 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L.
Inositol Urea Caffeic Acid Medium Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of a wide variety of microorganisms.
Inhibitory Mold Agar
259
Inositol Urea Caffeic Acid Medium Composition per liter: Agar solution .............................................. 900.0mL Base solution............................................... 100.0mL
Agar Solution: Composition per 900.0mL:
Composition per liter:
Agar ..................................................................15.0g
Agar ..................................................................15.0g Glucose ...............................................................5.0g Yeast extract........................................................5.0g Pancreatic digest of casein..................................3.0g Na2HPO4 .............................................................2.0g Peptic digest of animal tissue..............................2.0g Starch ..................................................................2.0g Dextrin ................................................................1.0g MgSO4·7H2O ......................................................0.8g MnSO4 ..............................................................0.16g Chloramphenicol.............................................0.125g FeSO4 ................................................................0.04g NaCl ..................................................................0.04g pH 6.7 ± 0.2 at 25°C
Preparation of Agar Solution: Add agar to dis-
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling with frequent agitation. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure– 121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the isolation of pathogenic fungi.
Inositol Brilliant Green Bile Salts Agar (IBB Agar) (Pleisomonas Differential Agar) Composition per liter: Agar ..................................................................15.0g meso-Inositol.....................................................10.0g Proteose peptone ...............................................10.0g Bile salts no. 3.....................................................8.5g Meat extract ........................................................5.0g NaCL...................................................................5.0g Neutral Red (2% solution) ............................ 1.25mL Brilliant Green (0.1% solution) .................... 0.33mL pH 7.2 ± 0.1 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the isolation of Aeromonas and Plesiomonas species.
tilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Base Solution: Composition per 100.0mL: Inositol ..............................................................10.0g Urea.....................................................................5.0g KH2PO4...............................................................1.0g MgSO4·7H2O ......................................................0.5g Caffeic acid .........................................................0.2g NaCl....................................................................0.1g CaCl2·2H2O ........................................................0.1g Gentamicin sulfate ............................................0.04g H3BO3 ..............................................................0.5mg ZnSO4·7H2O ....................................................0.4mg MnSO4·4H2O ...................................................0.4mg Thiamine·HCl ..................................................0.4mg Pyroxidine·HCl ................................................0.4mg Niacin...............................................................0.4mg Calcium pantothenate ......................................0.4mg p-Aminobenzoic acid.......................................0.2mg Riboflavin ........................................................0.2mg FeCl3 ................................................................0.2mg Na2MoO4·4H2O ...............................................0.2mg KI .....................................................................0.1mg CuSO4·5H2O ..................................................0.04mg Folic acid ..........................................................2.0µg Biotin ................................................................2.0µg Ferric citrate solution (1% solution) ............... 1.0mL
Preparation of Base Solution: Add components, except urea, to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Gently heat just until components are dissolved. Cool to 75°– 80°C. Add urea. Mix thoroughly. Do not heat after addition of urea. Do not autoclave. Filter sterilize.
Preparation of Medium: Aseptically combine the cooled, sterile agar solution with the sterile base solution. Mix thoroughly. Pour into sterile Petri dishes. Use: For the selective isolation and differentiation of Cryptococcus species based on inositol and urea utilization and pigment production from caffeic acid. On this medium, only Cryptococcus species utilize inositol as sole carbon source and urea as sole nitrogen source. Cryptococcus neoformans appears as
260
Intracellular Growth Phase Medium
dark brown colonies. Other Cryptococcus species are unpigmented.
Intracellular Growth Phase Medium (IGP Medium) Composition per 100.0mL: Gentamicin sulfate .......................................500.0mg Lysozyme .......................................................30.0mg Eagle MEM................................................... 72.0mL Dulbecco’s phosphate-buffered saline .......... 20.0mL Fetal bovine serum.......................................... 8.0mL pH 7.2–7.4 at 25°C
Eagle MEM: Composition per liter:
CaCl2 ...................................................................0.1g MnCl2·6H2O .......................................................0.1g
Preparation of Dulbecco’s Phosphate-Buffered Saline: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly.
Preparation of Medium: Combine components. Mix thoroughly. Filter sterilize. Aseptically distribute into sterile tubes or flasks.
Use: For the screening of Escherichia coli for pathogenicity using the HeLa cell test for invasiveness.
Ion Agar for Ureaplasma Composition per 101.45mL:
NaCl ....................................................................8.0g Glucose ...............................................................1.0g KCl......................................................................0.4g CaCl2·2H2O.......................................................0.14g MgSO4·7H2O ......................................................0.1g KH2PO4 .............................................................0.06g Na2HPO4 ...........................................................0.05g L-Isoleucine .....................................................0.026g L-Leucine.........................................................0.026g L-Lysine...........................................................0.026g L-Threonine .....................................................0.024g L-Valine .........................................................0.0235g L-Tyrosine........................................................0.018g L-Arginine .....................................................0.0174g L-Phenylalanine.............................................0.0165g L-Cystine .........................................................0.012g L-Histidine........................................................8.0mg L-Methionine ....................................................7.5mg Phenol Red.......................................................5.0mg L-Tryptophan ....................................................4.0mg Inositol .............................................................1.8mg Biotin ...............................................................1.0mg Folic acid..........................................................1.0mg Calcium pantothenate ......................................1.0mg Choline chloride...............................................1.0mg Nicotinamide....................................................1.0mg Pyridoxal·HCl ..................................................1.0mg Thiamine·HCl ..................................................1.0mg Riboflavin ........................................................0.1mg
HEPES (N-[2-Hydroxyethyl] piperazine-N´-[2-ethanesulfonic acid]) buffer ..................................1.19g Ionagar no. 2 .....................................................0.75g Pancreatic digest of casein..................................0.7g NaCl....................................................................0.5g Beef extract.........................................................0.3g Yeast extract........................................................0.3g Beef heart, solids from infusion..........................0.2g Yeast extract........................................................0.1g Horse serum, normal sterile.......................... 10.0mL Ampicillin solution ......................................... 1.0mL Urea solution................................................. 0.25mL Nystatin solution............................................. 0.1mL Tripeptide solution .......................................... 0.1mL pH 7.2 ± 0.2 at 25°C
Preparation of Eagle MEM: Add components
Nystatin Solution: Composition per 1.0mL:
to distilled/deionized water and bring volume to 1.0L. Mix thoroughly.
Dulbecco’s Phosphate-Buffered Saline: Composition per liter: NaCl ....................................................................8.0g Na2HPO4·7H2O.................................................2.16g KCl......................................................................0.2g KH2PO4 ...............................................................0.2g
Ampicillin Solution: Composition per 10.0mL: Ampicillin ...........................................................1.0g
Preparation of Ampicillin Solution: Add ampicillin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Urea Solution: Composition per 100.0mL: Urea...................................................................10.0g
Preparation of Urea Solution: Add urea to distilled/deionized water and bring volume to 100.0mL. Filter sterilize. Store at –20°C.
Nystatin........................................................ 50,000U
Preparation of Nystatin Solution: Add nystatin to distilled/deionized water and bring volume to 1.0mL. Filter sterilize. Tripeptide Solution: Composition per 10.0mL: Glycyl-L-histidyl-L-lysine acetate ....................0.2mg
Iso-Sensitest Agar Preparation of Tripeptide Solution: Add glycyl-L-histidyl-L-lysine acetate to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. Store at –20°C.
Preparation of Medium: Add components—except horse serum, ampicillin solution, urea solution, nystatin solution, and tripeptide solution—to distilled/deionized water and bring volume to 90.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 10.0mL of sterile horse serum, 1.0mL of sterile ampicillin solution, 0.25mL of sterile urea solution, 0.1mL of sterile nystatin solution, and 0.1mL of sterile tripeptide solution. Mix thoroughly. Pour into sterile Petri dishes.
Use: For the cultivation of Ureaplasma species from clinical specimens.
Irgasan Ticarcillin Chlorate Broth (ITC Broth) Composition per liter: MgCl2·6H20 ......................................................60.0g Pancreatic digest of casein................................10.0g NaCl ....................................................................5.0g KClO4 .................................................................1.0g Yeast extract........................................................1.0g Malachite Green (0.2% solution).................... 5.0mL Irgasan solution............................................... 1.0mL Ticarcillin solution .......................................... 1.0mL pH 7.6 ± 0.2 at 25°C
Irgasan Solution: Composition per 10.0mL: Irgasan (triclosan) ............................................1.0mg
Preparation of Irgasan Solution: Add Irgasan to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Ticarcillin Solution: Composition per 10.0mL: Ticarcillin ........................................................1.0 mg
Preparation of Ticarcillin Solution: Add ticarcillin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except Irgasan solution and ticarcillin solution, to distilled/deionized water and bring volume to 998.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Adjust to pH 7.6. Aseptically add 1.0mL of Irgasan solution and 1.0mL of ticarcillin solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the selective isolation and cultivation of Yersinia species.
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Iron Agar, Lyngby (Lyngby Iron Agar) Composition per liter: Peptone .............................................................20.0g Agar ..................................................................12.0g NaCl....................................................................5.0g Beef extract.........................................................3.0g Yeast extract........................................................3.0g L-Cysteine ...........................................................0.6g Ferric citrate........................................................0.3g Na2S2O3 ..............................................................0.3g pH 7.4 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and enumeration of H2Sproducing bacteria.
Iron Milk Medium Composition per liter: Iron filings ..........................................................1.0g Whole milk ........................................................ 1.0L pH 6.8 ± 0.2 at 25°C
Preparation of Medium: Add iron filings, which may be small balls of steel wool, to whole milk and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Use: For the cultivation of lactic acid bacteria. For the cultivation and differentiation of Clostridium species. The medium turns black if H2S is produced. The medium turns red if acid is produced from milk carbohydrate fermentation. Acid and gas production is characteristic of Clostridium perfringens and Clostridium butyricum.
Iso-Sensitest Agar Composition per liter: Casein, hydrolyzed ........................................... 11.0g Agar ....................................................................8.0g Peptones..............................................................3.0g NaCl....................................................................3.0g Na2HPO4 .............................................................2.0g Glucose ...............................................................2.0g Sodium acetate....................................................1.0g Soluble starch......................................................1.0g Magnesium glycerophosphate ............................0.2g
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Iso-Sensitest Broth
Calcium gluconate ..............................................0.1g L-Cysteine·HCl..................................................0.02g L-Tryptophan .....................................................0.02g Adenine.............................................................0.01g Guanine.............................................................0.01g Xanthine............................................................0.01g Uracil ................................................................0.01g Nicotinamide....................................................3.0mg Pantothenate.....................................................3.0mg Pyridoxine........................................................3.0mg MnCl2·4H2O ....................................................2.0mg CoSO4 ..............................................................1.0mg CuSO4·5H2O ....................................................1.0mg FeSO4·7H2O.....................................................1.0mg Menadione .......................................................1.0mg Cyanocobalamin ..............................................1.0mg ZnSO4·7H2O ....................................................1.0mg Biotin ...............................................................0.3mg Thiamine ........................................................0.04mg pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For antimicrobial susceptibility testing.
Iso-Sensitest Broth Composition per liter: Casein, hydrolyzed............................................11.0g Peptones ..............................................................3.0g NaCl ....................................................................3.0g Glucose ...............................................................2.0g Na2HPO4 .............................................................2.0g Sodium acetate....................................................1.0g Soluble starch......................................................1.0g Magnesium glycerophosphate ............................0.2g Calcium gluconate ..............................................0.1g L-cysteine·HCl ..................................................0.02g L-Tryptophan .....................................................0.02g Adenine.............................................................0.01g Guanine.............................................................0.01g Xanthine............................................................0.01g Uracil ................................................................0.01g Nicotinamide....................................................3.0mg Pantothenate.....................................................3.0mg Pyridoxine........................................................3.0mg MnCl2·4H2O ....................................................2.0mg CoSO4 ..............................................................1.0mg CuSO4·5H2O ....................................................1.0mg FeSO4·7H2O.....................................................1.0mg Menadione .......................................................1.0mg Cyanocobalamin ..............................................1.0mg
ZnSO4·7H2O ....................................................1.0mg Biotin ...............................................................0.3mg Thiamine ........................................................0.04mg pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For antimicrobial susceptibility testing.
Isoleucine Hydroxamate Medium Composition per liter: Agar ..................................................................15.0g K2HPO4...............................................................7.0g Glucose ...............................................................5.0g KH2PO4...............................................................3.0g L-Isoleucine hydroxamate ...................................1.0g (NH4)2SO4 ..........................................................1.0g pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of Serratia marcescens.
Jones-Kendrick Pertussis Transport Medium Composition per liter: Beef heart, solids from infusion......................500.0g Agar ..................................................................20.0g Soluble starch....................................................10.0g Tryptose ............................................................10.0g NaCl....................................................................5.0g Charcoal powder, activated.................................4.0g Yeast extract........................................................3.5g Penicillin solution ......................................... 10.0mL pH 7.4 ± 0.2 at 25°C
Penicillin Solution: Composition per 10.0mL: Penicillin ........................................................... 300U
Preparation of Penicillin Solution: Add penicillin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except penicillin solution, starch, yeast extract, heart infusion, and agar, to water. Boil to dissolve. Add charcoal, mix well, and autoclave. Cool to 50°C, add
Kanamycin Vancomycin Laked Blood Agar
263
penicillin, and dispense into small bottles as slants. Cool and seal tightly. Store at 5°C. Stable for 2 to 3 months.
Preparation of Vitamin K1 Solution: Add vita-
Use: For the cultivation and transport of Bordetella
Preparation of Medium: Add components, ex-
pertussis between clinical isolation and laboratory cultivation.
cept sheep blood, vancomycin, and vitamin K1 solution, to distilled/deionized water and bring volume to 939.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C. Aseptically add sheep blood, vancomycin solution, and 1.0mL vitamin K1 solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Jordan’s Tartrate Agar Composition per liter: Agar ..................................................................15.0g Pancreatic digest of casein................................10.0g Sodium potassium tartrate ................................10.0g NaCl ....................................................................5.0g Phenol Red......................................................0.024g pH 7.7 ± 0.3 at 25°C
Source: This medium is available as a prepared me-
min K1 to 99.0mL of absolute ethanol. Mix thoroughly. Filter sterilize.
Use: For the selective isolation of anaerobes, particularly Bacteroides, from clinical specimens.
Kanamycin Vancomycin Laked Blood Agar
dium in tubes from BD Diagnostic Systems.
Composition per liter:
Preparation of Medium: Add components to
Agar ..................................................................17.5g Pancreatic digest of casein................................15.0g Papaic digest of soybean meal............................5.0g NaCl....................................................................5.0g Kanamycin......................................................0.075g Sheep blood, laked........................................ 50.0mL Vancomycin solution .................................... 10.0mL Vitamin K1 solution ........................................ 1.0mL
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Adjust pH to 7.7. Distribute into tubes. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the differentiation and identification of members of the Enterobacteriaceae, especially Salmonella species, based upon the ability to utilize tartrate. Utilization of tartrate turns the medium yellow. Salmonella enteritidis utilizes tartrate. Salmonella paratyphi A does not utilize tartrate.
Kanamycin Vancomycin Blood Agar (KVBA) Composition per liter: Agar ..................................................................17.5g Pancreatic digest of casein................................15.0g Papaic digest of soybean meal ............................5.0g NaCl ....................................................................5.0g Kanamycin ..........................................................0.1g Sheep blood, defibrinated ............................. 50.0mL Vancomycin solution..................................... 10.0mL Vitamin K1 solution ........................................ 1.0mL
Vancomycin Solution: Composition per 10.0mL: Vancomycin .....................................................7.5mg
Preparation of Vancomycin Solution: Add vancomycin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. Vitamin K1 Solution: Composition per 100.0mL: Vitamin K1 ..........................................................1.0g
Vancomycin Solution: Composition per 10.0mL: Vancomycin .....................................................7.5mg
Preparation of Vancomycin Solution: Add vancomycin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. Vitamin K1 Solution: Composition per 100.0mL: Vitamin K1 ..........................................................1.0g
Preparation of Vitamin K1 Solution: Add vitamin K1 to 99.0mL of absolute ethanol. Mix thoroughly. Filter sterilize.
Preparation of Medium: The blood is laked (hemolyzed) by freezing whole blood overnight and then thawing. Add components, except sheep blood, vancomycin, and vitamin K1 solution, to distilled/ deionized water and bring volume to 939.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sheep blood, vancomycin solution, and 1.0mL of vitamin K1 solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For isolation of the Bacteroides melaninogenicus group.
264
Kasai Medium
Kasai Medium Composition per liter: Pancreatic digest of casein................................20.0g Soluble starch....................................................20.0g L-Cysteine·HCl·H2O ...........................................5.0g K2HPO4 ...............................................................5.0g NaCl ....................................................................5.0g Yeast extract........................................................2.0g
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the isolation and cultivation of Leptotrichia buccalis from saliva and plaque.
KCN Broth Composition per liter: Na2HPO4 ...........................................................5.64g NaCl ....................................................................5.0g Peptone................................................................3.0g KH2PO4 ...........................................................0.225g KCN (0.5% solution) .................................... 15.0mL pH 7.6 ± 0.2 at 25°C
Caution: Cyanide is toxic. Preparation of Medium: Add components, except KCN solution, to distilled/deionized water and bring volume to 985.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C. Aseptically add KCN solution. Mix thoroughly. Aseptically distribute into sterile tubes. Stopper immediately.
Use: For the differentiation of Enterobacteriaceae based upon growth in the presence of potassium cyanide.
Keister's Modified TYI-S-33 Medium Composition per liter: Pancreatic digest of casein................................20.0g Glucose .............................................................10.0g Yeast extract......................................................10.0g L-Cysteine·HCl ...................................................2.0g NaCl ....................................................................2.0g K2HPO4 ...............................................................1.0g Bovine bile........................................................0.75g KH2PO4 ...............................................................0.6g Ascorbic acid ......................................................0.2g Ferric ammonium citrate................................22.8mg Bovine serum, heat inactivated................... 100.0mL
Preparation of Medium: Add components, except bovine serum, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Aseptically add
1.0L of sterile, heat-inactivated bovine serum. Mix thoroughly. Aseptically distribute into sterile, screwcapped tubes or flasks.
Use: For the cultivation of Giardia cati, Giardia intestinalis, and Hexamita species.
Kelly Medium, Nonselective Modified Composition per 1430.0mL: HEPES buffer (N-2-HydroxyethylpiperazineN-2-ethanesulfonic acid) ..............................6.0g Proteose peptone no. 2........................................5.0g D-Glucose ............................................................3.0g NaHCO3 ..............................................................2.2g Pancreatic digest of casein..................................1.0g Yeast, autolyzed ..................................................1.0g Sodium pyruvate.................................................0.8g Sodium citrate.....................................................0.7g N-Acetylglucosamine .........................................0.4g MgCl2·6H2O .......................................................0.3g Gelatin solution........................................... 200.0mL Bovine serum albumin................................ 143.0mL CMRL-1066 medium with glutamine, 10X............................. 100.0mL Rabbit serum, heat inactivated...................... 86.0mL Hemin solution................................................ 1.0mL pH 7.2 ± 0.2 at 25°C
CMRL-1066 Medium with Glutamine, 10X: Composition per liter: NaCl....................................................................6.8g NaHCO3 ..............................................................2.2g D-Glucose ............................................................1.0g KCl......................................................................0.4g L-Cysteine·HCl·H2O..........................................0.26g CaCl2, anhydrous ................................................0.2g MgSO4·7H2O ......................................................0.2g NaH2PO4·H2O...................................................0.14g L-Glutamine ........................................................0.1g Sodium acetate·3H2O......................................0.083g L-Glutamic acid...............................................0.075g L-Arginine·HCl..................................................0.07g L-Lysine·HCl .....................................................0.07g L-Leucine ..........................................................0.06g Glycine..............................................................0.05g Ascorbic acid ....................................................0.05g L-Proline............................................................0.04g L-Tyrosine .........................................................0.04g L-Aspartic acid ..................................................0.03g L-Threonine .......................................................0.03g L-Alanine.........................................................0.025g L-Phenylalanine...............................................0.025g L-Serine ...........................................................0.025g L-Valine ...........................................................0.025g L-Cystine ...........................................................0.02g L-Histidine·HCl·H2O.........................................0.02g
Kelly Medium, Selective Modified
265
L-Isoleucine .......................................................0.02g
Preparation of Hemin Solution: Add hemin to
Phenol Red........................................................0.02g L-Methionine ...................................................0.015g Deoxyadenosine................................................0.01g Deoxycytidine...................................................0.01g Deoxyguanosine................................................0.01g Glutathione, reduced.........................................0.01g Thymidine.........................................................0.01g Hydroxy-L-proline.............................................0.01g L-Tryptophan .....................................................0.01g Nicotinamide adenine dinucleotide .................7.0mg Tween 80..........................................................5.0mg Sodium glucuronate·H2O.................................4.2mg Coenzyme A ....................................................2.5mg Cocarboxylase..................................................1.0mg Flavin adenine dinucleotide .............................1.0mg Nicotinamide adenine dinucleotide phosphate ..............................1.0mg Uridine triphosphate ........................................1.0mg Choline chloride...............................................0.5mg Cholesterol .......................................................0.2mg 5-Methyldeoxycytidine....................................0.1mg Inositol ...........................................................0.05mg p-Aminobenzoic acid.....................................0.05mg Niacin...........................................................0.025mg Niacinamide .................................................0.025mg Pyridoxine....................................................0.025mg Pyridoxal·HCl ..............................................0.025mg Biotin .............................................................0.01mg D-Calcium pantothenate .................................0.01mg Folic acid........................................................0.01mg Riboflavin ......................................................0.01mg Thiamine·HCl ................................................0.01mg pH 7.2 ± 0.2 at 25°C
20.0mL of 1N NaOH solution. Mix thoroughly. Bring volume to 100.0mL with distilled/deionized water.
Bovine Serum Albumin Solution: Composition per 200.0mL: Bovine serum albumin......................................70.0g
Preparation of Bovine Serum Albumin Solution: Add bovine serum albumin to distilled/deionized water and bring volume to 200.0mL. Filter sterilize.
Preparation of Medium: Add components, except gelatin solution, bovine serum albumin solution, and rabbit serum, to distilled/deionized water and bring volume to 1001.0mL. Mix thoroughly. Bring pH to 7.6 with 5N NaOH. Filter sterilize. Aseptically add 200.0mL of sterile gelatin solution, 143.0mL of sterile bovine serum albumin, and 86.0mL of sterile heat-inactivated rabbit serum. Mix thoroughly. Aseptically dispense into sterile tubes or flasks.
Use: For the isolation of Borrelia burgdorferi and other spirochetes.
Kelly Medium, Selective Modified Composition per 1270mL:
deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.2. Filter sterilize.
Bovine serum albumin fraction V.....................50.0g HEPES buffer (N-2-HydroxyethylpiperazineN-2-ethanesulfonic acid) ..............................6.0g Glucose ...............................................................5.0g Neopeptone .........................................................5.0g NaHCO3 ..............................................................2.2g Sodium pyruvate.................................................0.8g Sodium citrate.....................................................0.7g N-Acetylglucosamine .........................................0.4g Kanamycin.......................................................8.0mg 5-Fluorouracil ..................................................2.3mg Gelatin solution........................................... 200.0mL CMRL-1066 medium with glutamine, 10X............................. 100.0mL Rabbit serum, partially hemolyzed ............... 70.0mL pH 7.7 ± 0.2 at 25°C
Gelatin Solution: Composition per 200.0mL:
Gelatin Solution: Composition per 200.0mL:
Source: This solution is available as a premixed powder from BD Diagnostics.
Preparation of CMRL-1066 Medium with Glutamine, 10X: Add components to distilled/
Gelatin...............................................................14.0g
Gelatin...............................................................14.0g
Preparation of Gelatin Solution: Add gelatin to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C.
Preparation of Gelatin Solution: Add gelatin to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C.
Hemin Solution: Composition per 100.0mL:
CMRL-1066 Medium with Glutamine, 10X: Composition per liter:
Hemin..................................................................1.0g NaOH (1N solution)...................................... 20.0mL
NaCl....................................................................6.8g NaHCO3 ..............................................................2.2g
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KF Streptococcus Agar
D-Glucose ............................................................1.0g
KCl......................................................................0.4g L-Cysteine·HCl·H2O..........................................0.26g CaCl2, anhydrous ................................................0.2g MgSO4·7H2O ......................................................0.2g NaH2PO4·H2O...................................................0.14g L-Glutamine.........................................................0.1g Sodium acetate·3H2O......................................0.083g L-Glutamic acid ...............................................0.075g L-Arginine·HCl..................................................0.07g L-Lysine·HCl .....................................................0.07g L-Leucine...........................................................0.06g Glycine..............................................................0.05g Ascorbic acid ....................................................0.05g L-Proline ............................................................0.04g L-Tyrosine..........................................................0.04g L-Aspartic acid ..................................................0.03g L-Threonine .......................................................0.03g L-Alanine.........................................................0.025g L-Phenylalanine...............................................0.025g L-Serine ...........................................................0.025g L-Valine ...........................................................0.025g L-Cystine ...........................................................0.02g L-Histidine·HCl·H2O .........................................0.02g L-Isoleucine .......................................................0.02g Phenol Red........................................................0.02g L-Methionine ...................................................0.015g Deoxyadenosine................................................0.01g Deoxycytidine...................................................0.01g Deoxyguanosine................................................0.01g Glutathione, reduced.........................................0.01g Thymidine.........................................................0.01g Hydroxy-L-proline.............................................0.01g L-Tryptophan .....................................................0.01g Nicotinamide adenine dinucleotide .................7.0mg Tween 80..........................................................5.0mg Sodium glucuronate·H2O.................................4.2mg Coenzyme A ....................................................2.5mg Cocarboxylase..................................................1.0mg Flavin adenine dinucleotide .............................1.0mg Nicotinamide adenine dinucleotide phosphate ..............................1.0mg Uridine triphosphate ........................................1.0mg Choline chloride...............................................0.5mg Cholesterol .......................................................0.2mg 5-Methyldeoxycytidine....................................0.1mg Inositol ...........................................................0.05mg p-Aminobenzoic acid.....................................0.05mg Niacin...........................................................0.025mg Niacinamide .................................................0.025mg Pyridoxine....................................................0.025mg Pyridoxal·HCl ..............................................0.025mg Biotin .............................................................0.01mg D-Calcium pantothenate .................................0.01mg Folic acid........................................................0.01mg
Riboflavin ......................................................0.01mg Thiamine·HCl ................................................0.01mg pH 7.2 ± 0.2 at 25°C
Source: This solution is available as a premixed powder from BD Diagnostics.
Preparation of CMRL-1066 Medium with Glutamine, 10X: Add components to distilled/ deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.2. Filter sterilize.
Preparation of Medium: Add components, except gelatin solution, partially hemolyzed rabbit serum solution, kanamycin, and 5-fluorouracil, to distilled/ deionized water and bring volume to 1.0L. Mix thoroughly. Bring pH to 7.6 with 5N NaOH. Filter sterilize. Aseptically add 200.0mL of sterile gelatin solution, 70.0mL of partially hemolyzed rabbit serum, 8.0mg of kanamycin, and 230.0mg of 5-fluorouracil. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the isolation of Borrelia burgdorferi.
KF Streptococcus Agar Composition per liter: Agar ..................................................................20.0g Maltose .............................................................20.0g Proteose peptone...............................................10.0g Sodium glycerophosphate.................................10.0g Yeast extract......................................................10.0g NaCl....................................................................5.5g Lactose................................................................1.0g NaN3 ...................................................................0.4g Bromcresol Purple ..........................................0.015g 2,3,5-Triphenyltetrazolium chloride solution ..................................... 10.0mL pH 7.2 ± 0.2 at 25°C
Caution: Sodium azide is toxic. Azides also react with metals and disposal must be highly diluted.
Source: This medium is available as a premixed powder from BD Diagnostic Systems and Oxoid Unipath.
2,3,5-Triphenyltetrazolium Chloride Solution: Composition per 10.0mL: 2,3,5-Triphenyltetrazolium chloride ...................0.1g
Preparation of 2,3,5-Triphenyltetrazolium Chloride Solution: Add 2,3,5-triphenyltetrazolium chloride to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except 2,3,5-triphenyltetrazolium chloride solution, to distilled/deionized water and bring volume to
Kirchner’s Enrichment Medium 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C. Aseptically add 2,3,5-triphenyltetrazolium chloride solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation and enumeration of enterococci.
KF Streptococcus Agar Composition per liter: Agar ..................................................................20.0g Maltose..............................................................20.0g Sodium glycerophosphate.................................10.0g Yeast extract......................................................10.0g NaCl ....................................................................5.0g Pancreatic digest of casein..................................5.0g Peptic digest of animal tissue..............................5.0g Lactose ................................................................1.0g NaN3 ...................................................................0.4g 2,3,5-Triphenyltetrazolium chloride solution ..................................... 10.0mL pH 7.2 ± 0.2 at 25°C
Caution: Sodium azide is toxic. Azides also react
267
Pancreatic digest of casein..................................5.0g Peptic digest of animal tissue .............................5.0g Lactose................................................................1.0g Na2CO3 ...........................................................0.636g NaN3 ...................................................................0.4g Phenol Red......................................................0.018g 2,3,5-Triphenyltetrazolium chloride solution ..................................... 10.0mL pH 7.2 ± 0.2 at 25°C
Caution: Sodium azide is toxic. Azides also react with metals and disposal must be highly diluted.
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components, except 2,3,5-triphenyltetrazolium chloride solution, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C. Aseptically add 2,3,5-triphenyltetrazolium chloride solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the selective cultivation of fecal streptococci.
with metals and disposal must be highly diluted.
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
2,3,5-Triphenyltetrazolium Chloride Solution: Composition per 10.0mL: 2,3,5-Triphenyltetrazolium chloride ...................0.1g
Preparation of 2,3,5-Triphenyltetrazolium Chloride Solution: Add 2,3,5-triphenyltetrazolium chloride to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, ex-
Kirchner’s Enrichment Medium Composition per liter: Na2HPO4·12H2O...............................................19.0g Asparagine ..........................................................5.0g KH2PO4...............................................................2.5g Sodium citrate.....................................................2.5g MgSO4 ................................................................0.6g Serum.......................................................... 100.0mL Glycerol ........................................................ 20.0mL Penicillin solution ......................................... 10.0mL Phenol Red (0.4% solution)............................ 3.0mL pH 7.4–7.6 at 25°C
cept 2,3,5-triphenyltetrazolium chloride solution, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C. Aseptically add 2,3,5-triphenyltetrazolium chloride solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Penicillin Solution: Composition per 10.0mL:
Use: For the selective cultivation and enumeration
cept serum and penicillin solution, to distilled/deionized water and bring volume to 890.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile serum and penicillin solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
of fecal streptococci.
KF Streptococcus Broth Composition per liter: Maltose..............................................................20.0g Sodium glycerophosphate.................................10.0g Yeast extract......................................................10.0g NaCl ....................................................................5.0g
Penicillin .................................................... 100,000U
Preparation of Penicillin Solution: Add penicillin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, ex-
Use: For the cultivation and enrichment of Mycobacterium species.
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K-L Virulence Agar
K-L Virulence Agar (Klebs-Loeffler Virulence Agar) (Elek Agar) (Corynebacterium diphtheriae Virulence Test Medium) Composition per 1300.0mL: K-L agar base..................................................... 1.0L Rabbit serum ............................................... 200.0mL K2TeO3 solution .......................................... 100.0mL K-L filter strips ....................................................100 pH 7.8 ± 0.2 at 25°C
Source: This medium is available as a premixed
Corynebacterium diphtheriae that produce toxin form white precipitin lines at approximately 45° angles from the culture streak line.
K-L Virulence Agar (Klebs-Loeffler Virulence Agar) Composition per 1250.0mL: K-L agar base..................................................... 1.0L K-L enrichment........................................... 200.0mL K2TeO3 solution............................................ 50.0mL K-L filter strips ....................................................100 pH 7.8 ± 0.2 at 25°C
powder from BD Diagnostic Systems.
Source: This medium is available as a premixed
K-L Agar Base: Composition per liter:
powder from BD Diagnostic Systems.
Meat peptone.....................................................20.0g Agar ..................................................................15.0g NaCl ....................................................................2.5g
Preparation of K-L Agar Base: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C.
K2TeO3 Solution: Composition per 100.0mL: K2TeO3 ................................................................0.3g
K-L Agar Base: Composition per liter: Meat peptone ....................................................20.0g Agar ..................................................................15.0g NaCl....................................................................2.5g
Preparation of K-L Agar Base: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C.
K-L Enrichment: Composition per 200.0mL:
Preparation of K2TeO3 Solution: Add K2TeO3
to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Casamino acids ...................................................4.0g Glycerol ...................................................... 100.0mL Tween 80..................................................... 100.0mL
Caution: Potassium tellurite is toxic.
Preparation of K-L Enrichment: Combine
K-L Filter Strips: Composition: Whatman no. 3 filter paper ........................ as needed Diphtheria toxin solution .............................. 10.0mL
Preparation of K-L Strips: Cut Whatman no. 3 filter paper into 1.5cm × 7cm strips. Autoclave for 15 min at 15 psi pressure–121°C. Aseptically dip each strip into a sterile solution containing 1000U of purified diphtheria toxin/mL. Drain off excess liquid. Preparation of Medium: Filter sterilize rabbit serum. To 1.0L of cooled, sterile K-L agar base, aseptically add sterile rabbit serum and sterile K2TeO3 solution. Mix thoroughly. Pour into sterile Petri dishes in 13.0mL volumes. Before the agar solidifies, aseptically add one K-L filter strip across the diameter of the plate. Allow the filter strip to sink to the bottom of the plate or press it down with sterile forceps. Allow the agar to solidify. Dry the surface of the plates by incubating at 35°C with lid of plate ajar for 2h.
Use: For in vitro toxigenicity testing of Corynebacterium diphtheriae by the agar diffusion technique.
components. Mix thoroughly. Filter sterilize.
K2TeO3 Solution: Composition per 100.0mL: K2TeO3 ................................................................1.0g
Preparation of K2TeO3 Solution: Add K2TeO3
to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Caution: Potassium tellurite is toxic. K-L Filter Strips: Composition: Diphtheria toxin solution .............................. 10.0mL Whatman no. 3 filter paper ........................ as needed
Preparation of K-L Strips: Cut Whatman no. 3
filter paper into 1.5cm × 7cm strips. Autoclave for 15 min at 15 psi pressure–121°C. Aseptically dip each strip into a sterile solution containing 1000U of purified diphtheria toxin/mL. Drain off excess liquid.
Preparation of Medium: To 1.0L of cooled, sterile K-L agar base, aseptically add sterile K-L enrichment and sterile K2TeO3 solution. Mix thoroughly.
Klebsiella Selective Agar
269
Pour into sterile Petri dishes in 13.0mL volumes. Before the agar solidifies, aseptically add one K-L filter strip across the diameter of the plate. Allow the filter strip to sink to the bottom of the plate or press it down with sterile forceps. Allow the agar to solidify. Dry the surface of the plates by incubating at 35°C with lid of plate ajar for 2h.
deionized water and bring volume to 30.0mL. Mix thoroughly.
Use: For in vitro toxigenicity testing of Corynebac-
carbenicillin to distilled/deionized water and bring volume to 1.0mL. Mix thoroughly. Filter sterilize.
terium diphtheriae by the agar diffusion technique. Corynebacterium diphtheriae that produce toxin form white precipitin lines at approximately 45° angles from the culture streak line.
Klebsiella Medium (m-Klebsiella Medium) Composition per 1041.0mL: Agar ..................................................................15.0g Adonitol ..............................................................4.0g 2× Salt solution ........................................... 500.0mL Uric acid solution........................................ 200.0mL Sodium taurocholate solution ....................... 30.0mL Phenol Red solution ...................................... 10.0mL Carbenicillin solution...................................... 1.0mL
2X Salt Solution: Composition per liter: KCl......................................................................8.0g K2HPO4 ...............................................................3.0g NaCl ....................................................................2.0g KH2PO4 ...............................................................1.0g MgSO4·7H2O ......................................................0.2g
Preparation of 2X Salt Solution: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly.
Uric Acid Solution: Composition per 200.0mL: Uric acid..............................................................0.3g
Preparation of Uric Acid Solution: Dissolve uric acid in a small volume of 1N NaOH. Bring volume to 200.0mL with distilled/deionized water. Adjust pH to 7.1 with 1N HCl. Filter sterilize.
Phenol Red Solution: Composition per 10.0mL: Phenol Red..........................................................0.1g
Preparation of Phenol Red Solution: Add Phenol Red to sterile distilled/deionized water and bring volume to 10.0mL. Mix thoroughly.
Sodium Taurocholate Solution: Composition per 30.0mL: Sodium taurocholate ...........................................0.4g
Preparation of Sodium Taurocholate Solution: Add sodium taurocholate to sterile distilled/
Carbenicillin Solution: Composition per 1.0mL: Carbenicillin ....................................................5.0mg
Preparation of Carbenicillin Solution: Add
Preparation of Medium: Add adonitol and agar to 500.0mL of 2× salt solution. Bring volume to 800.0mL with distilled/deionized water. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 200.0mL of uric acid solution, 30.0mL of sodium taurocholate solution, 10.0mL of Phenol Red solution, and 1.0mL of carbenicillin solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the enumeration of Klebsiella species by the membrane filter method.
Klebsiella Selective Agar Composition per liter: Agar ..................................................................26.0g DL–Phenylalanine .............................................10.0g L-Ornithine·HCl ................................................10.0g Raffinose.............................................................7.0g Pancreatic digest of casein..................................2.5g Yeast extract........................................................2.5g K2HPO4...............................................................2.0g Phenol Red solution...................................... 10.0mL Carbenicillin solution.................................... 10.0mL pH 5.6 ± 0.2 at 25°C
Phenol Red Solution: Composition per 10.0mL: Phenol Red..........................................................0.5g
Preparation of Phenol Red Solution: Add Phenol Red to 50% ethanol and bring volume to 10.0mL. Mix thoroughly.
Preparation of Medium: Add components, except carbenicillin solution, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 10.0mL carbenicillin solution. Mix thoroughly. Adjust pH to 5.6–5.7 with sterile 1N HCl. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation and identification of Klebsiella pneumoniae from clinical specimens.
270
Kligler Iron Agar
Kligler Iron Agar
Kligler Iron Agar (FDA M71)
Composition per liter: Peptone..............................................................20.0g Agar ..................................................................12.0g Lactose ..............................................................10.0g NaCl ....................................................................5.0g Beef extract .........................................................3.0g Yeast extract........................................................3.0g Glucose ...............................................................1.0g Ferric citrate........................................................0.3g Na2S2O3 ..............................................................0.3g Phenol Red........................................................0.05g pH 7.4 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems and Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the differentiation and identification of Enterobacteriaceae based upon sugar fermentation and hydrogen sulfide production. Sugar fermentation is indicated by the medium turning yellow. H2S production results in the medium turning black.
Kligler Iron Agar Composition per liter: Agar ..................................................................15.0g Lactose ..............................................................10.0g Pancreatic digest of casein................................10.0g Peptic digest of animal tissue............................10.0g NaCl ....................................................................5.0g Glucose ...............................................................1.0g Ferric ammonium citrate.....................................0.5g Na2S2O3 ..............................................................0.5g Phenol Red......................................................0.025g pH 7.4 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the differentiation and identification of Enterobacteriaceae based upon sugar fermentation and hydrogen sulfide production. Sugar fermentation is indicated by the medium turning yellow. H2S production results in the medium turning black.
Composition per liter: Lactose..............................................................20.0g Agar ..................................................................15.0g Pancreatic digest of casein................................10.0g Peptic digest of animal tissue ...........................10.0g NaCl....................................................................5.0g Glucose ...............................................................1.0g Ferric ammonium citrate.....................................0.5g Na2S2O3 ..............................................................0.5g Phenol Red......................................................0.025g pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the differentiation and identification of Enterobacteriaceae based upon sugar fermentation and hydrogen sulfide production. Sugar fermentation is indicated by the medium turning yellow. H2S production results in the medium turning black.
Knisely Medium for Bacillus anthracis Composition per liter: Beef heart, solids from infusion......................500.0g Agar ..................................................................15.0g Pancreatic digest of casein................................10.0g NaCl....................................................................5.0g EDTA ...........................................................200.0mg Lysozyme.......................................................40.0mg Thallous acetate .............................................40.0mg Polymyxin.................................................... 30,000U
Preparation of Medium: Add components, except EDTA, lysozyme, thallous acetate, and polymyxin, to distilled/deionized water and bring volume to 1.0mL. Mix thoroughly. Gently heat and bring to boiling. Adjust pH to 7.3. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile EDTA, lysozyme, thallous acetate, and polymyxin. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation and maintenance of Bacillus anthracis.
Koch’s K1 Medium Composition per liter: Glucose ...............................................................1.8g Peptone ...............................................................0.6g Yeast extract........................................................0.4g
Kupferberg Trichomonas Base Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
271
tribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–56°C. Aseptically add 100.0mL of rabbit serum. Mix thoroughly.
Use: For the cultivation of Leptospira species.
Use: For the cultivation of a variety of fungi.
Korthof Medium Composition per 1088.0mL: NaCl ....................................................................1.4g Na2HPO4·2H2O.................................................0.88g Peptone................................................................0.8g KH2PO4 .............................................................0.24g CaCl2 .................................................................0.04g KCl....................................................................0.04g NaHCO3 ............................................................0.02g Rabbit serum, inactivated ............................. 80.0mL Rabbit hemoglobin solution............................ 8.0mL pH 7.2 ± 0.2 at 25°C
Rabbit Hemoglobin Solution: Composition per 20.0mL: Rabbit blood clot........................................... 10.0mL
Preparation of Rabbit Hemoglobin Solution: Add rabbit blood clot to 10.0mL of distilled/deionized water. Lyse the clot by freezing and thawing.
Preparation of Medium: Add components, except rabbit serum and rabbit hemoglobin solution, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Cool to 25°C. Filter through Whatman no. 1 filter paper. Distribute into flasks in 100.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°– 50°C. Aseptically add 8.0mL of rabbit serum and 0.8mL of rabbit hemoglobin solution to each flask. Mix thoroughly.
Use: For the cultivation of Leptospira species.
Korthof Medium, Modified Composition per liter: NaCl ....................................................................1.4g Na2HPO4·2H2O.................................................0.88g Peptone................................................................0.8g KH2PO4 .............................................................0.24g CaCl2 .................................................................0.04g KCl....................................................................0.04g NaHCO3 ............................................................0.02g Rabbit serum, heat inactivated at 56°C....... 100.0mL pH 7.2–7.6 at 25°C
Preparation of Medium: Add components, except rabbit serum, to distilled/deionized water and bring volume to 900.0L. Mix thoroughly. Gently heat and bring to boiling. Boil for 20 min. Cool overnight at 4°C. Filter through Whatman no. 2 filter paper. Dis-
Koser Citrate Medium Composition per liter: Sodium citrate.....................................................3.0g NaNH4HPO4·4H2O.............................................1.5g KH2PO4...............................................................1.0g MgSO4·7H2O ......................................................0.2g pH 6.7 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the differentiation of Escherichia coli and Enterobacter aerogenes based on citrate utilization.
Kosmachev’s Medium Composition per liter: Agar ..................................................................15.0g CaCO3 .................................................................4.0g KNO3 ..................................................................1.0g (NH4)2SO4 ..........................................................1.0g Na2HPO4 .............................................................1.0g MgSO4·7H2O ......................................................0.5g FeSO4·7H2O......................................................0.01g Yeast autolysate (30% solution) ................... 15.0mL
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the isolation and cultivation of Actinomadura species, Actinopolyspora species, Excellospora species, and Microspora species.
Kupferberg Trichomonas Base Composition per liter: Pancreatic digest of casein................................20.0g L-Cysteine·HCl·H2O ...........................................1.5g Agar ....................................................................1.0g Maltose ...............................................................1.0g Methylene Blue................................................3.0mg Bovine serum ................................................ 50.0mL pH 6.0 ± 0.2 at 25°C
272
Kupferberg Trichomonas Broth
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components, except bovine serum, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 50.0mL of bovine serum. If desired, additional selectivity can be obtained by aseptically adding 250,000U of penicillin and 1.0g of streptomycin or 1.0g of chloramphenicol. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation of the Trichomonas species from clinical specimens.
Kupferberg Trichomonas Broth Composition per liter: Enzymatic digest of protein ..............................20.0g L-Cysteine·HCl·H2O ...........................................1.5g Agar ....................................................................1.0g Maltose................................................................1.0g Chloramphenicol.................................................0.1g Methylene Blue................................................3.0mg Bovine serum ................................................ 50.0mL pH 6.0 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components, except bovine serum, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add bovine serum. If desired, additional selectivity can be obtained by aseptically adding 250,000U penicillin and 1.0g streptomycin or 1.0g chloramphenicol. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation of the Trichomonas species from clinical specimens.
L Agar (Luria Agar) Composition per liter: Agar ..................................................................15.0g Pancreatic digest of casein................................10.0g Yeast extract........................................................5.0g NaCl ....................................................................0.5g Glucose solution ........................................... 20.0mL pH 7.0 ± 0.2 at 25°C
Glucose Solution: Composition per 100.0mL: Glucose .............................................................10.0g
Preparation of Glucose Solution: Add glucose to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize. Preparation of Medium: Add components, except glucose solution, to distilled/deionized water and bring volume to 980.0mL. Mix thoroughly. Bring pH to 7.0. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Aseptically add 20.0mL of sterile glucose solution. Mix thoroughly. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation of Escherichia coli.
L Broth (Luria Broth) Composition per liter: Pancreatic digest of casein................................10.0g NaCl....................................................................5.0g Yeast extract........................................................5.0g Glucose ...............................................................1.0g
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of Escherichia coli.
L Diphasic Blood Agar Medium (ATCC Medium 947) Composition per 1150.0mL: Blood agar, diphasic base medium ............. 700.0mL Rabbit blood, defibrinated .......................... 300.0mL Locke’s solution.......................................... 150.0mL pH 7.2–7.4 at 25°C
Blood Agar, Diphasic Base Medium: Composition per 750.0mL: Beef...................................................................25.0g Agar ..................................................................10.0g Neopeptone .......................................................10.0g NaCl....................................................................2.5g
Preparation of Blood Agar, Diphasic Base Medium: Trim beef to remove fat. Add 25.0g of lean beef to 250.0mL of distilled/deionized water. Gently heat and bring to boiling. Boil for 2–3 min. Filter through Whatman no. 2 filter paper. Add agar, neopeptone, and NaCl to filtrate. Bring volume to 750.0mL with distilled/deionized water. Mix thoroughly. Adjust pH to 7.2–7.4. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 50°–55°C.
Lactose Broth
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Locke's Solution: Composition per liter:
CaCl2 .................................................................. 0.2g KCl......................................................................0.2g
NaCl ....................................................................8.0g Glucose ...............................................................2.5g KH2PO4 .............................................................. 0.3g CaCl2 .................................................................. 0.2g KCl......................................................................0.2g
Preparation of Locke's Solution: Add compo-
Preparation of Locke's Solution: Add compo-
700.0mL of sterile blood agar, diphasic base medium, with 300.0mL of sterile defibrinated rabbit blood warmed to 50°–55°C. Mix thoroughly. Aseptically distribute 5.0mL volumes into 16 × 125mm screwcapped test tubes. Allow to cool in a slanted position. Overlay the agar in each tube with 3.0mL of sterile Locke’s solution.
nents to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C.
Preparation of Medium: Aseptically combine 700.0mL of sterile blood agar, diphasic base medium, with 300.0mL of sterile defibrinated rabbit blood warmed to 50°–55°C. Mix thoroughly. Aseptically distribute 5.0mL volumes into 16 × 125mm screwcapped test tubes. Allow to cool in a slanted position. Overlay the agar in each tube with 1.0mL of sterile Locke’s solution. Use: For the cultivation and maintenance of Trypanosoma species, Leishmania donovani, Herpetomonas species, and Trypanosoma neveulemairei.
L Diphasic Blood Agar Medium (ATCC Medium 1011) Composition per 1150.0mL: Blood agar, diphasic base medium ............. 700.0mL Rabbit blood, defibrinated .......................... 300.0mL Locke’s solution.......................................... 150.0mL pH 7.2–7.4 at 25°C
Blood Agar, Diphasic Base Medium: Composition per 750.0mL: Beef...................................................................25.0g Agar ..................................................................10.0g Neopeptone .......................................................10.0g NaCl ....................................................................2.5g
Preparation of Blood Agar, Diphasic Base Medium: Trim beef to remove fat. Add 25.0g of lean beef to 250.0mL of distilled/deionized water. Gently heat and bring to boiling. Boil for 2–3 min. Filter through Whatman no. 2 filter paper. Add agar, neopeptone, and NaCl to filtrate. Bring volume to 750.0mL with distilled/deionized water. Mix thoroughly. Adjust pH to 7.2–7.4. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 50°–55°C.
Locke's Solution: Composition per liter: NaCl ....................................................................8.0g Glucose ...............................................................2.5g KH2PO4 .............................................................. 0.3g
nents to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C.
Preparation of Medium: Aseptically combine
Use: For the cultivation and maintenance of Trypanosoma species.
Lab-Lemco Agar Composition per liter: Agar ..................................................................15.0g Peptone ...............................................................5.0g Lab-lemco meat extract ......................................3.0g pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of a variety of heterotrophic microorganisms.
Lactose Broth Composition per liter: Lactose................................................................5.0g Pancreatic digest of gelatin.................................5.0g Beef extract.........................................................3.0g pH 6.9 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems and Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes containing an inverted Durham tube in 10.0mL volumes. Autoclave for 12 min at 15 psi pressure–121°C. Cool broth quickly to 25°C. For testing water samples with 10.0mL volumes, prepare medium double strength.
Use: For the detection of lactose-fermenting, Gramnegative coliforms, as a preenrichment broth for Salmonella species, and in the study of lactose fermentation of bacteria in general.
274
Lactose Egg Yolk Milk Agar
Lactose Egg Yolk Milk Agar Composition per 1206.0mL: Lactose ..............................................................12.0g Agar ....................................................................1.0g Columbia blood agar base........................... 800.0mL Skim milk.................................................... 150.0mL Egg yolk emulsion, 50%............................... 36.0mL Inhibitor solution........................................... 20.0mL Neutral Red (1% solution) ............................ 3.25mL pH 7.0 ± 0.2 at 25°C
Columbia Blood Agar Base: Composition per 800.0mL: Agar ..................................................................15.0g Pantone..............................................................10.0g Bitone................................................................10.0g NaCl ....................................................................5.0g Tryptic digest of beef heart .................................3.0g Cornstarch...........................................................1.0g
Preparation of Columbia Blood Agar Base: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat until boiling.
Egg Yolk Emulsion, 50%: Composition per 100.0mL: Chicken egg yolks..................................................11 Whole chicken egg...................................................1 NaCl (0.9% solution) .................................... 50.0mL
Preparation of Egg Yolk Emulsion, 50%: Soak eggs with 1:100 dilution of saturated mercuric chloride solution for 1 min. Crack eggs and separate yolks from whites. Mix egg yolks with 1 chicken egg. Beat to form emulsion. Measure 50.0mL of egg yolk emulsion and add to 50.0mL of 0.9% NaCl solution. Mix thoroughly. Filter sterilize. Warm to 45°–50°C.
Inhibitor Solution: Composition per 20.0mL: Neomycin sulfate ..............................................0.18g NaN3 .................................................................0.24g
of sterile inhibitor solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation and maintenance of Clostridium species.
Lactose Gelatin Medium Composition per liter: Gelatin.............................................................120.0g Tryptose ............................................................15.0g Lactose..............................................................10.0g Yeast extract......................................................10.0g Phenol Red (0.5% solution).......................... 10.0mL pH 7.5 ± 0.2 at 25°C
Preparation of Medium: Add tryptose, yeast extract, and lactose to distilled/deionized water and bring volume to 400.0mL. Mix thoroughly. Add gelatin to distilled/deionized water and bring volume to 590.0mL. Gently heat gelatin solution while stirring and bring to 50°–60°C. Add Phenol Red. Mix the two solutions together. Distribute into tubes in 10.0mL volumes. Autoclave for 10 min at 15 psi pressure– 121°C. If medium is not used in 8 hr, deoxygenate by heating to 50°–70°C for 2–3 hr prior to inoculation.
Use: For the cultivation of Clostridium perfringens.
Lash Serum Medium Composition per liter: Casamino acids .................................................14.0g NaCl....................................................................6.0g Glucose ...............................................................2.0g Maltose ...............................................................1.5g Sodium lactate (60% solution)............................0.5g KCl......................................................................0.1g CaCl2·2H2O ........................................................0.1g Serum solution ............................................ 500.0mL pH 5.8 ± 0.2 at 25°C
Serum Solution: Composition per 500.0mL:
Caution: Sodium azide is toxic. Azides also react
NaHCO3 ..............................................................0.1g Bovine serum .............................................. 200.0mL
with metals and disposal must be highly diluted.
Preparation of Serum Solution: Add compo-
Preparation of Inhibitor Solution: Add neo-
nents to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Filter sterilize.
mycin sulfate and NaN3 to distilled/deionized water and bring volume to 20.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Combine Columbia blood agar base, lactose, agar, and Neutral Red and bring volume to 1.0L. Adjust pH to 7.0. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 55°C. Filter sterilize skim milk. To 1.0L of cooled, sterile agar mixture, aseptically add 150.0mL of sterile skim milk, 36.0mL of sterile egg yolk emulsion, 50%, and 20.0mL
Preparation of Medium: Add components, except serum solution, to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Distribute into tubes in 5.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C. Aseptically add 5.0mL of sterile serum solution to each tube. Mix thoroughly.
Use: For the cultivation of Trichomonas vaginalis from clinical specimens.
Lead Acetate Agar
Lauryl Sulfate Broth (m-Lauryl Sulfate Broth) Composition per liter: Peptone..............................................................39.0g Lactose ..............................................................30.0g Yeast extract........................................................6.0g Sodium lauryl sulfate ..........................................1.0g Phenol Red..........................................................0.2g pH 7.4 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into bottles or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation and enumeration of coliform bacteria, especially Escherichia coli, by the membrane filter method.
Lauryl Sulfate Broth (Lauryl Tryptose Broth) Composition per liter: Pancreatic digest of casein................................20.0g Lactose ................................................................5.0g NaCl ....................................................................5.0g K2HPO4 .............................................................2.75g KH2PO4 .............................................................2.75g Sodium lauryl sulfate ..........................................0.1g pH 6.8 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes containing an inverted Durham tube in 10.0mL volumes. Autoclave for 12 min at 15 psi pressure–121°C. Cool broth quickly to 25°C. For testing water samples with 10.0mL volumes, prepare medium double strength.
Use: For the detection of coliform bacteria in a variety of specimens. Also, for the enumeration of coliform bacteria by the multiple-tube fermentation technique.
Lauryl Sulfate Broth with MUG Composition per liter: Pancreatic digest of casein................................20.0g Lactose ................................................................5.0g NaCl ....................................................................5.0g K2HPO4 .............................................................2.75g KH2PO4 .............................................................2.75g Sodium lauryl sulfate ..........................................0.1g
275
4-Methylumbellferylβ-D-glucuronide (MUG) .............................0.05g pH 6.8 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes containing an inverted Durham tube in 10.0mL volumes. Autoclave for 12 min at 15 psi pressure–121°C. Cool broth quickly to 25°C. For testing water samples with 10.0mL volumes, prepare medium double strength.
Use: For the detection of Escherichia coli by a fluorogenic procedure.
LB Agar Composition per liter: Agar ..................................................................15.0g Pancreatic digest of casein................................10.0g NaCl....................................................................5.0g Yeast extract........................................................5.0g 1N NaOH ........................................................ 1.0mL pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Adjust pH to 7.0. Distribute into tubes or flasks. Autoclave for 25 min at 15 psi pressure–121°C. Pour into sterile Petri dishes in 35–40.0mL volumes.
Use: For the cultivation of Escherichia coli.
Lead Acetate Agar Composition per liter: Agar ..................................................................15.0g Peptone .............................................................15.0g Proteose peptone.................................................5.0g Glucose ...............................................................1.0g Lead acetate ........................................................0.2g Na2S2O3 ............................................................0.08g pH 6.6 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes. Allow tubes to cool in a slanted position.
Use: For the cultivation and differentiation of Gramnegative coliform bacteria based on H2S production. Bacteria that produce H2S turn the medium brown.
276
Lecithin Lactose Agar
Lecithin Lactose Agar Composition per liter: Agar ..................................................................15.0g Pancreatic digest of casein................................12.7g Lactose ..............................................................10.0g NaCl ....................................................................5.5g Peptic digest of animal tissue..............................5.5g Yeast extract........................................................3.9g Pancreatic digest of heart muscle........................3.3g Cornstarch...........................................................1.1g Egg lecithin .......................................................0.66g L-Cysteine·HCl·H2O............................................0.5g NaN3 ...................................................................0.2g Neomycin sulfate ..............................................0.15g CaCl2 .................................................................0.05g Bromcresol Purple ............................................0.02g pH 6.8 ± 0.2 at 25°C
Caution: Sodium azide is toxic. Azides also react with metals and disposal must be highly diluted.
Source: This medium is available as a prepared medium from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes.
Use: For the isolation, cultivation, and differentiation of histolytic clostridia from clinical specimens based on lecithinase production and lactose fermentation. It is especially useful for the differentiation of Clostridium perfringens, Clostridium sordelli, Clostridium novyi, Clostridium septicum, and Clostridium histolyticum. Bacteria that produce lecithinase appear as colonies surrounded by an opalescent zone. Bacteria that ferment lactose appear as colonies surrounded by a yellow zone.
Lecithin Lipase Anaerobic Agar Composition per liter: Pancreatic digest of casein................................40.0g Agar ..................................................................25.0g Yeast extract........................................................5.0g Na2HPO4·12H2O.................................................5.0g Glucose ...............................................................2.0g NaCl ....................................................................2.0g KH2PO4 ...............................................................1.0g MgSO4·7H2O ......................................................0.1g Egg yolk emulsion ...................................... 100.0mL pH 7.6 ± 0.2 at 25°C
Egg Yolk Emulsion: Composition: Chicken egg yolks..................................................11 Whole chicken egg...................................................1
Preparation of Egg Yolk Emulsion: Soak eggs with 1:100 dilution of saturated mercuric chloride solution for 1 min. Crack eggs and separate yolks from whites. Mix egg yolks with 1 chicken egg. Filter sterilize.
Preparation of Medium: Add components, except egg yolk emulsion, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile egg yolk emulsion. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation, cultivation, and differentiation of Clostridium species based on lecithinase production and lipase production. Bacteria that produce lecithinase appear as colonies surrounded by a zone of insoluble precipitate. Bacteria that produce lipase appear as colonies with a pearly iridescent sheen.
Lecithin Tween Medium (LT Medium) Composition per liter: Tween 80...........................................................30.0g Agar ..................................................................15.0g Pancreatic digest of casein................................10.0g Peptic digest of animal tissue ...........................10.0g NaCl....................................................................5.0g Lecithin ...............................................................5.0g Na2S2O3·5H2O ....................................................5.0g Glycerol ..............................................................3.0g Histidine, free base .............................................1.0g Glucose ...............................................................1.0g pH 7.5 ± 0.2 at 25°C
Antibiotic Solution: Composition per 10.0mL: 5–Fluorocytosine ................................................0.2g Fosfomicin ..........................................................0.1g Ticarcillin............................................................0.1g
Preparation of Antibiotic Solution: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except antibiotic solution, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile antibiotic solution. Mix thoroughly. Pour into sterile Petri dishes in 20.0mL volumes.
Use: For the isolation and cultivation of multiresistant lipophilic Corynebacterium species, especially Corynebacterium group JK found primarily in infec-
Legionella Selective Agar tions in immuno-compromised hosts and patients with prosthetic valve endocarditis.
Legionella Agar Base (Legionella Medium) (BCYEα Agar, Modified) Composition per liter: Agar ..................................................................17.0g Yeast extract......................................................10.0g ACES buffer (N-2-acetamido2-aminoethane sulfonic acid) .......................6.0g Charcoal, activated..............................................1.5g KOH....................................................................1.5g α-Ketoglutarate...................................................1.0g Legionella agar enrichment .......................... 10.0mL pH 6.85–7.0 at 25°C
Source: This medium is available as a prepared medium from BD Diagnostic Systems.
Legionella Agar Enrichment: Composition per 10.0mL: L-Cysteine·HCl·H2O............................................0.4g
Fe4(P2O7)3 .........................................................0.25g
Preparation of Legionella Agar Enrichment: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
277
Agar Phase: Composition per 500.0mL: Agar ..................................................................17.0g Charcoal, activated .............................................2.0g
Preparation of Agar Phase: Add components to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Gently heat and bring to boiling. Distribute in 20.0mL volumes into 125.0mL serum bottles with aluminum crimp seals and rubber stoppers. Autoclave for 20 min at 15 psi pressure– 121°C. Cool to 50°C. Swirl medium to put charcoal in suspension. Allow agar to solidify so that a slant with a 6.0cm height is formed.
Broth Phase: Composition per 500.0mL: Yeast extract......................................................20.0g L-Cysteine·HCl·H2O solution..............................0.4g Fe(NO3)3·9H2O solution .....................................0.1g
Preparation of Broth Phase: Add yeast extract to distilled/deionized water and bring volume to 480.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C. Aseptically add sterile L-cysteine·HCl·H2O solution and Fe(NO3)3·9H2O solution. Mix thoroughly. Adjust pH to 6.9 with 6.0mL of sterile 1N KOH. L-Cysteine·HCl·H2O
Solution: Composition per 10.0mL:
Preparation of Medium: Add components, ex-
L-Cysteine·HCl·H2O .........................................0.04g
cept Legionella agar enrichment, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50° C. Add 10.0mL of sterile Legionella agar enrichment. Adjust pH to 6.9 at 50°C by adding 4.0–4.5mL of 1.0N KOH. This is a critical step. Mix thoroughly. Pour into sterile Petri dishes in 20.0mL volumes. Swirl medium while pouring to keep charcoal in suspension.
Preparation of L-Cysteine·HCl·H2O Solution: Add L-cysteine·HCl·H2O to distilled/deionized
Use: For the preparation of Legionella agars. For the isolation and cultivation of Legionella species from clinical and nonclinical materials.
Legionella pneumophila Medium (Charcoal Yeast Extract Diphasic Blood Culture Medium) (Diphasic Blood Culture Buffered Charcoal Yeast Extract Medium) (CYE-DBCM) Composition per liter: Agar phase .................................................. 500.0mL Broth phase ................................................. 500.0mL pH 6.9–7.0 at 25°C
water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Fe(NO3)3·9H2O Solution: Composition per 10.0mL: Fe(NO3)3·9H2O.................................................0.04g
Preparation of Fe(NO3)3·9H2O Solution: Add Fe(NO3)3 to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add 20.0mL of sterile broth phase to 125.0mL serum bottles containing 20.0mL of solidified agar phase. Seal bottles by crimping metal caps over rubber stoppers. Use: For the isolation and cultivation of Legionella pneumophila from blood cultures.
Legionella Selective Agar Composition per liter: Agar ..................................................................15.0g ACES (2-[(2-Amino-2-oxoethyl)-amino]ethane sulfonic acid) buffer ...............................10.0g Yeast extract......................................................10.0g
278
Leishmania Medium
Charcoal, activated..............................................2.0g α-Ketoglutarate...................................................1.0g L-Cysteine·HCl·H2O solution........................ 10.0mL Fe4(P2O7)3 solution ....................................... 10.0mL Antibiotic solution ........................................ 10.0mL pH 6.85–7.0 at 25°C
Source: This medium is available as a prepared medium from BD Diagnostic Systems. L-Cysteine·HCl·H2O
Solution: Composition per 10.0mL: L-Cysteine·HCl·H2O............................................0.4g
Preparation of L-Cysteine·HCl·H2O Solution: Add L-cysteine·HCl·H2O to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Fe4(P2O7)3 Solution: Composition per 10.0mL: Fe4(P2O7)3 .........................................................0.25g
Preparation of Fe4(P2O7)3 Solution: Add Fe4(P2O7)3 to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. Antibiotic Solution: Composition per 10.0mL: Anisomycin....................................................10.0mg Colistin...........................................................3.75mg Vancomycin .....................................................2.0mg
Preparation of Antibiotic Solution: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components—except L-cysteine·HCl·H2O, Fe4(P2O7)3 and antibiotic solutions—to distilled/deionized water and bring volume to 970.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C. Aseptically add sterile Lcysteine·HCl·H2O, Fe4(P2O7)3 and antibiotic solutions. Mix thoroughly. Pour into sterile Petri dishes. Swirl medium while pouring to keep charcoal in suspension.
Use: Legionella selective agar is used in qualitative procedures for the isolation of Legionella species from clinical and nonclinical specimens.
Leishmania Medium Composition per 100.0mL: Sodium citrate .....................................................1.2g NaCl ....................................................................1.0g Rabbit blood solution.................................... 10.0mL
Rabbit Blood Solution: Composition per 10.0mL: Rabbit blood, defibrinated .............................. 5.0mL
Preparation of Rabbit Blood Solution: Add 5.0mL of whole rabbit blood to 5.0mL of sterile distilled/deionized water. Freeze and thaw twice to lyse blood cells. Preparation of Medium: Add components, except rabbit blood solution, to distilled/deionized water and bring volume to 90.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Aseptically add 10.0mL of sterile rabbit blood solution. Mix thoroughly. Aseptically distribute into sterile, screw-capped tubes or flasks.
Use: For the cultivation of Leishmania donovani, Leishmania hertigi, and Leishmania tropica.
Leptospira Medium Composition per liter: (NH4)2Fe(SO4)2·6H2O ........................................6.0g NaH2PO4 ...........................................................0.53g L-Asparagine .......................................................0.5g Glycerol ..............................................................0.2g Tween 60.............................................................0.2g MgSO4·7H2O ....................................................0.15g KH2PO4...........................................................0.069g Tween 80...........................................................0.05g EDTA ................................................................0.01g CaCO3 ..............................................................4.0mg Thiamine·HCl ..................................................1.0mg Vitamin B12 .......................................................1.0µg pH 7.4–7.6 at 25°C
Preparation of Medium: Add components, except thiamine·HCl, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Aseptically add 1.0mg of thiamine·HCl. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation of Leptospira species.
Leptospira Medium, EMJH (Leptospira Medium, Ellinghausen-McCullough/ Johnson-Harris) Composition per liter: Na2HPO4 .............................................................1.0g NaCl....................................................................1.0g KH2PO4...............................................................0.3g NH4Cl ...............................................................0.25g Thiamine ..........................................................5.0mg Rabbit serum............................................... 100.0mL pH 7.5 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Leptotrichia buccalis Medium Preparation of Medium: Add components, except rabbit serum, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C. Aseptically add sterile rabbit serum. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation and maintenance of Leptospira species.
Leptospira Medium, Modified Composition per liter:
279
Cyanocobalamin (0.02% solution) ................. 1.0mL Glycerol (10% solution) ................................. 1.0mL KH2PO4 (1% solution).................................... 1.0mL MnSO4·H2O (0.1% solution) .......................... 1.0mL ZnSO4 (0.4% solution) ................................... 0.1mL pH 7.6 ± 0.2 at 25°C
CT-Tween 60: Composition per 200.0mL: Charcoal, Norit A..............................................40.0g Tween 60...........................................................20.0g
Preparation of CT-Tween 60: Add Tween 60 to
Agar ....................................................................1.5g NaCl ....................................................................0.5g Peptone................................................................0.3g Beef extract .........................................................0.2g Hemin solution................................................ 2.5mL Sterile rabbit serum ..................................... 100.0mL pH 7.3 ± 0.1 at 25°C
200.0mL of distilled/deionized water. Mix thoroughly. While stirring, add charcoal. Stir mixture for 18 hr at 25°C. Allow charcoal to settle out of suspension for 18 hr at 4°C. Carefully decant the Tween solution off the sediment. Centrifuge the Tween solution at 10,000 × g for 1h. Decant supernatant solution. Pass Tween solution through a thin-channel ultrafiltration XM 100 membrane. Store stock solution at −20°C.
Hemin Solution: Composition per 100.0mL:
CT-Tween 40: Composition per 200.0mL:
Hemin................................................................0.05g NaOH (1N solution)........................................ 1.0mL
Preparation of Hemin Solution: Add hemin to 1.0mL of 1N NaOH solution. Mix thoroughly. Bring volume to 100.0mL with distilled/deionized water. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Preparation of Medium: Add components, except hemin solution and rabbit serum, to distilled/ deionized water and bring volume to 897.5mL. Mix thoroughly. Gently heat and bring to boiling. Adjust pH to 7.4. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C. Aseptically add 2.5mL of sterile hemin solution and 100.0mL of sterile rabbit serum. Mix thoroughly. The pH of the medium should be 7.3. Store at 4°C for 24h. Inactivate medium at 56°C for 60 min. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation and maintenance of Leptospira species.
Leptospira Protein-Free Medium (Leptospira PF Medium) Composition per liter: TES (N-Tris[hydroxymethyl]methyl-2-aminoethane sulfonic acid) buffer .....................................1.2g NaCl ....................................................................0.9g Sodium pyruvate .................................................0.2g CT-Tween 60................................................. 12.0mL CT-Tween 40................................................... 3.0mL MgCl2-CaCl2 solution..................................... 1.0mL
Charcoal, Norit A..............................................40.0g Tween 40...........................................................20.0g
Preparation of CT-Tween 40: Add Tween 40 to 200.0mL of distilled/deionized water. Mix thoroughly. While stirring, add charcoal. Stir mixture for 18 hr at 25°C. Allow charcoal to settle out of suspension for 18 hr at 4°C. Carefully decant the Tween solution off the sediment. Centrifuge the Tween solution at 10,000 × g for 1h. Decant supernatant solution. Pass Tween solution through a thin-channel ultrafiltration XM 100 membrane. Store stock solution at −20°C.
MgCl2–CaCl2 Solution: Composition per 100.0mL: CaCl2·2H2O ........................................................1.5g MgCl2·6H2O .......................................................1.5g
Preparation of MgCl2-CaCl2 Solution: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation of Leptospira species.
Leptotrichia buccalis Medium Composition per liter: Agar ..................................................................15.0g Nutrient broth......................................................8.0g Yeast extract........................................................2.0g Glucose solution ........................................... 10.0mL
280
Leptotrichia Medium
solution........................ 10.0mL Hemin solution................................................ 4.0mL pH 7.2–7.6 at 25°C
Whatman #1 filter paper. Autoclave filtrate for 15 min at 15 psi pressure–121°C.
Glucose Solution: Composition per 10.0mL: Preparation of Glucose Solution: Add glucose to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
cept horse serum and tomato decoction, to distilled/ deionized water and bring volume to 850.0mL. Mix thoroughly. Gently heat and bring to boiling. Adjust pH to 7.2–7.4. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C. Aseptically add sterile horse serum and tomato decoction. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
L-Cysteine·HCl·H2O
Use: For the cultivation and maintenance of Leptot-
L-Cysteine·HCl·H2O
D-Glucose ............................................................2.0g
Solution: Composition per 10.0mL: L-Cysteine·HCl·H2O............................................1.0g
Preparation of L-Cysteine·HCl·H2O Solution: Add L-cysteine·HCl·H2O to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Hemin Solution: Composition per 10.0mL: Hemin...............................................................2.5mg Triethanolamine (50% solution) ................... 10.0mL
Preparation of Hemin Solution: Add hemin to 10.0mL of triethanolamine solution. Mix thoroughly.
Preparation of Medium: Add components, ex-
Preparation of Medium: Add components, ex-
richia buccalis.
Letheen Agar Composition per liter: Agar ..................................................................15.0g Tween 80.............................................................7.0g Pancreatic digest of casein..................................5.0g Beef extract.........................................................3.0g Glucose ...............................................................1.0g Lecithin ...............................................................1.0g pH 7.0 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
cept glucose solution, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile glucose solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Preparation of Medium: Add components to
Use: For the cultivation and maintenance of Leptot-
Use: For determination of the antimicrobial activity
richia buccalis.
Leptotrichia Medium Composition per liter: Pancreatic digest of casein................................10.0g NaCl ....................................................................5.0g Peptone................................................................5.0g Yeast extract........................................................3.0g Na2HPO4 .............................................................2.5g L-Cysteine·HCl·H2O............................................0.5g Horse serum ................................................ 100.0mL Tomato decoction.......................................... 50.0mL pH 7.2–7.4 at 25°C
Tomato Decoction: Composition per 100.0mL: Tomatoes ....................................................... 50.0mL
Preparation of Tomato Decoction: Mince fresh tomatoes and measure 50.0mL. Add 50.0mL of tap water. Mix thoroughly. Gently heat and bring to boiling. Continue boiling for 10 min. Filter through
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes. of quaternary ammonium compounds.
Letheen Agar, Modified Composition per liter: Agar ..................................................................20.0g Thiotone............................................................10.0g Pancreatic digest of casein................................10.0g Tween 80.............................................................7.0g NaCl................................................................... 5.0g Beef extract.........................................................3.0g Yeast extract........................................................2.0g Glucose ...............................................................1.0g Lecithin ...............................................................1.0g NaHSO3 ..............................................................0.1g pH 7.2 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes.
Listeria Enrichment Broth Use: For determination of the antimicrobial activity of quaternary ammonium compounds.
Letheen Broth
281
Eosin Y ...............................................................0.4g Methylene Blue............................................0.065mg pH 7.1 ± 0.2 at 25°C
Source: This medium is available as a premixed
Composition per liter:
powder from BD Diagnostic Systems.
Peptic digest of animal tissue............................10.0g Beef extract .........................................................5.0g NaCl ....................................................................5.0g Tween 80.............................................................5.0g Lecithin ...............................................................0.7g pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Add components to
Source: This medium is available as a premixed
Use: For the isolation, cultivation, and differentiation of Gram-negative enteric bacteria based on lactose fermentation. Bacteria that ferment lactose, especially the coliform bacterium Escherichia coli, appear as colonies with a green metallic sheen or blue-black to brown color. Bacteria that do not ferment lactose appear as colorless or transparent light purple colonies.
powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For determination of the antimicrobial activity of quaternary ammonium compounds.
Levinthal’s Agar Composition per 105.0mL:
Letheen Broth, Modified Composition per liter: Peptic digest of animal tissue............................10.0g Thiotone peptone ..............................................10.0g Beef extract .........................................................5.0g NaCl ....................................................................5.0g Tween 80.............................................................5.0g Pancreatic digest of casein..................................5.0g Yeast extract........................................................2.0g Lecithin ...............................................................0.7g NaHSO3 ..............................................................0.1g pH 7.2 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into screw-capped bottles in 90.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For determination of the antimicrobial activity of quaternary ammonium compounds.
Levine EMB Agar (Levine Eosin Methylene Blue Agar) (Eosin Methylene Blue Agar, Levine) (LEMB Agar) Composition per liter: Agar ..................................................................15.0g Lactose ..............................................................10.0g Peptone..............................................................10.0g K2HPO4 ...............................................................2.0g
Nutrient agar, sterile ................................... 100.0mL Rabbit blood or human blood, sterile ............. 5.0mL pH 6.8 ± 0.2 at 25°C
Nutrient Agar: Composition per liter: Agar ..................................................................15.0g Pancreatic digest of gelatin.................................5.0g Beef extract.........................................................3.0g
Source: Nutrient agar is available as a premixed powder from BD Diagnostic Systems.
Preparation of Nutrient Agar: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Preparation of Medium: To 100.0mL of cooled, sterile nutrient agar, aseptically add 5.0mL of human blood or rabbit blood. Mix thoroughly. Heat in a boiling water bath for 5 min. Allow the deposit to settle out of suspension. Pour the clear supernatant solution into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation of Haemophilus species.
Listeria Enrichment Broth Composition per liter: Pancreatic digest of casein................................17.0g Yeast extract........................................................6.0g NaCl....................................................................5.0g Papaic digest of soybean meal............................3.0g
282
Listeria Fermentation Broth
Glucose ...............................................................2.5g K2HPO4 ...............................................................2.5g Cycloheximide ..................................................0.05g Nalidixic acid ....................................................0.04g Acriflavine·HCl...............................................0.015g pH 7.3 ± 0.2 at 25°C
Preparation of Acridine Solution: Add acridine to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Preparation of Medium: Add components, ex-
Use: For the isolation and cultivation of Listeria
cept acridine solution, to distilled/deionized water and bring volume to 998.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add acridine solution. Mix thoroughly. Aseptically distribute into sterile tubes in 10.0mL volumes or fill bottles 4/5s full.
monocytogenes according to the FDA formula.
Use: For the maintenance—as a transport medium—
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Listeria Fermentation Broth Composition per liter: Proteose peptone no. 3 ......................................10.0g NaCl ....................................................................5.0g Beef extract .........................................................1.0g Bromcresol Purple ..............................................0.1g Carbohydrate solution................................... 10.0mL
and enrichment of Listeria species.
LIT Medium Composition per liter:
carbohydrate to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. Use glucose, salicin, rhamnose, dulcitol, or raffinose.
Beef liver, infusion from.................................453.0g Na2HPO4 .............................................................8.0g Pancreatic digest of casein..................................5.0g Tryptose ..............................................................5.0g Glucose ...............................................................1.0g NaCl....................................................................1.0g K2HPO4...............................................................0.5g KCl..................................................................... 0.4g Hemin ............................................................10.0mg Fetal bovine serum, heat inactivated .......... 100.0mL pH 7.2 ± 0.2 at 25°C
Preparation of Medium: Add components, ex-
Preparation of Medium: Add components to
cept carbohydrate solution, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile carbohydrate solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation of Herpetomonas mariadea-
Use: For the cultivation and differentiation of Liste-
Composition per liter:
Carbohydrate Solution: Composition per 10.0mL: Carbohydrate.......................................................5.0g
Preparation of Carbohydrate Solution: Add
ria species based on the fermentation of glucose, salicin, rhamnose, dulcitol, and raffinose.
Listeria Transport Enrichment Medium Composition per liter:
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.2. Filter sterilize. Aseptically distribute into sterile tubes or flasks. nei, Trypanoplasma borreli, and Trypanosoma cruzi.
Litmus Milk Skim milk........................................................100.0g Azolitmin ............................................................0.5g Na2SO3 ................................................................0.5g pH 6.5 ± 0.2 at 25°C
Source: This medium is available as a premixed
Sodium glycerophosphate.................................10.0g Agar ....................................................................2.0g Sodium thioglycolate ..........................................1.0g CaCl2 ...................................................................0.1g Nalidixic acid ....................................................0.04g Acridine solution............................................. 2.0mL pH 7.4 ± 0.2 at 25°C
powder from BD Diagnostic Systems and Oxoid Unipath.
Acridine Solution: Composition per 10.0mL:
Use: For the maintenance of lactic acid bacteria and for the differentiation of several bacteria, especially Clostridium species, based on their action on milk.
Acridine ............................................................0.04g
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 20 min at 10 psi pressure–115°C.
Liver Veal Agar
283
Bacteria that do not ferment carbohydrates, such as Proteus vulgaris or Moraxella lacunata, show no change in the azolitimin litmus indicator. Bacteria that ferment lactose or glucose with the production of gas, such as Clostridium perfringens, turn the medium pink and frothy. Bacteria that proteolytically degrade milk lactalbumin turn the medium blue. Bacteria that coagulate milk casein form a curd or clot. Bacteria that peptonize casein, such as Pseudomonas aeruginosa, show a dissolution of the clot.
starch. Bring volume to 1.0L with distilled/deionized water. Refilter solution. Add meat particles to test tubes to a depth of approximately 2cm. Distribute broth into tubes with meat particles in 15.0mL volumes. Autoclave for 20 min at 15 psi pressure–121°C.
Littman Oxgall Agar
Beef liver, infusion from.................................500.0g Agar ..................................................................20.0g Proteose peptone...............................................10.0g NaCl....................................................................5.0g pH 6.9 ± 0.2 at 25°C
Composition per liter: Agar ..................................................................20.0g Oxgall................................................................15.0g Glucose .............................................................10.0g Peptone..............................................................10.0g Crystal Violet ....................................................0.01g Streptomycin solution ................................... 10.0mL pH 6.5 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Streptomycin Solution: Composition per 10.0mL: Streptomycin .....................................................0.03g
Preparation of Streptomycin Solution: Add streptomycin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except streptomycin solution, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile streptomycin solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes. Allow tubes to cool in a slanted position.
Use: For the selective isolation and cultivation of fungi, especially dermatophytes.
Liver Broth Composition per liter: Beef liver, fresh...............................................453.0g Pancreatic digest of casein................................10.0g K2HPO4 ...............................................................1.0g Soluble starch......................................................1.0g pH 7.6 ± 0.2 at 25°C
Preparation of Medium: Remove the fat from fresh beef liver. Grind the liver. Add 1.0L of distilled/ deionized water. Gently heat and bring to boiling. Continue boiling for 60 min. Adjust pH to 7.6. Filter through cheesecloth. Reserve meat. To filtrate, add pancreatic digest of casein, K2HPO4, and soluble
Use: For the isolation and cultivation of anaerobic microorganisms, especially Clostridium botulinum.
Liver Infusion Agar Composition per liter:
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation of Brucella species and other fastidious pathogenic bacteria.
Liver Infusion Broth Composition per liter: Beef liver, infusion from.................................500.0g Proteose peptone...............................................10.0g NaCl....................................................................5.0g pH 6.9 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of Brucella species and other fastidious pathogenic bacteria.
Liver Veal Agar Composition per liter: Veal, infusion from .........................................500.0g Beef liver, infusion from...................................50.0g Gelatin...............................................................20.0g Proteose peptone...............................................20.0g Agar ..................................................................15.0g Soluble starch....................................................10.0g Glucose ...............................................................5.0g
284
Liver Veal Egg Yolk Agar
NaCl ....................................................................5.0g Casein..................................................................2.0g NaNO3.................................................................2.0g Enzymatic digest of protein ................................1.3g Pancreatic digest of casein ..................................1.3g pH 7.3 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Make sure that some liver and veal particles are transferred to each tube. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation of a variety of anaerobic organisms.
Liver Veal Egg Yolk Agar Composition per 1080.0mL: Liver veal agar ................................................... 1.0L Egg yolk emulsion, 50%............................... 80.0mL pH 7.3 ± 0.2 at 25°C
Liver Veal Agar: Composition per liter: Veal, infusion from .........................................500.0g Beef liver, infusion from...................................50.0g Gelatin...............................................................20.0g Proteose peptone ...............................................20.0g Agar ..................................................................15.0g Soluble starch....................................................10.0g Glucose ...............................................................5.0g NaCl ....................................................................5.0g Casein..................................................................2.0g NaNO3.................................................................2.0g Enzymatic digest of protein ................................1.3g Pancreatic digest of casein ..................................1.3g
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Liver Veal Agar: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Make sure that some liver and veal particles are transferred to each tube. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 50°C.
Egg Yolk Emulsion, 50%: Composition per 100.0mL: Chicken egg yolks..................................................11 Whole chicken egg...................................................1 NaCl (0.9% solution) .................................... 50.0mL
Preparation of Egg Yolk Emulsion, 50%: Soak eggs with 1:100 dilution of saturated mercuric chloride solution for 1 min. Crack eggs and separate yolks from whites. Mix egg yolks with 1 chicken egg. Beat to form emulsion. Measure 50.0mL of egg yolk emulsion and add to 50.0mL of 0.9% NaCl solution. Mix thoroughly. Filter sterilize. Warm to 45°–50°C.
Preparation of Medium: To 1.0L of cooled sterile liver veal agar, aseptically add 80.0mL of sterile egg yolk emulsion, 50%. Mix thoroughly. Pour into sterile Petri dishes. Dry plates at 35°C for 24h.
Use: For the cultivation of a variety of anaerobic organisms.
LMX Broth Modified, Fluorocult (Fluorocult LMX Broth, Modified) Composition per liter: Tryptose ..............................................................5.0g NaCl....................................................................5.0g Sorbitol ...............................................................1.0g Tryptophan..........................................................1.0g K2HPO4...............................................................2.7g KH2PO4...............................................................2.0g Lauryl sulfate sodium salt...................................0.1g 5-Bromo-4-chloro-3-indolyl-β-Dgalactopyran_oside (X-GAL).......................0.08 4-Methylumbelliferyl-β-D-glucuronide ............0.05g 1-Isopropyl-β-D-1-thio-galactopyranoside IPTG) .............................................................0.1 pH: 6.8 ± 0.2 at 25°C
Source: This medium is available from Merck. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into into test tubes Autoclave for 15 min at 15 psi pressure–121°C. The broth is clear and yellowish brown.
Use: For the simultaneous detection of total coliforms and E. coli by the fluorogenic procedure. A color change of the broth from yellow to blue-green indicates the presence of coliforms. A blue fluorescence under long-wave UV light permits the rapid detection of E.coli. As tryptophan is added to the broth, the indole reaction is easily done by adding KOVACS reagent. The formation of a red ring additionally confirms the presence of E.coli.
Loeffler Blood Serum Medium Composition per liter: Beef blood serum........................................ 750.0mL Dextrose broth ............................................ 250.0mL pH 7.1 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Loeffler Slant, Modified Dextrose Broth: Composition per liter: Tryptose ............................................................10.0g Glucose ...............................................................5.0g Sodium chloride..................................................5.0g Beef extract .........................................................3.0g
Preparation of Dextrose Broth: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly.
Preparation of Medium: Combine 750.0mL of beef blood serum with 250.0mL of dextrose broth. Mix thoroughly. Distribute into screw-capped tubes. Slant tubes in the autoclave. Close the autoclave door loosely. Autoclave for 10 min at 0 psi pressure– 100°C. Close the autoclave door tightly. Autoclave for 15 min at 15 psi pressure–121°C. Use: For the cultivation of Corynebacterium diphtheriae. For demonstration of pigment production and proteolysis by Corynebacterium diphtheriae.
Loeffler Blood Serum Medium Composition per liter: Beef blood serum ........................................ 750.0mL Dextrose broth............................................. 250.0mL pH 7.1 ± 0.2 at 25°C
Dextrose Broth: Composition per liter: Enzymatic digest of protein ................................2.5g Glucose .............................................................1.25g NaCl ..................................................................1.25g Beef extract .......................................................0.75g
Preparation of Dextrose Broth: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly.
Preparation of Medium: Combine 750.0mL of beef blood serum with 250.0mL of dextrose broth. Mix thoroughly. Distribute into screw-capped tubes. Slant tubes in the autoclave. Close the autoclave door loosely. Autoclave for 10 min at 0 psi pressure– 100°C. Close the autoclave door tightly. Autoclave for 15 min at 15 psi pressure–121°C.
285
Peptic digest of animal tissue ...........................0.71g NaCl..................................................................0.36g pH 7.6 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into screw-capped tubes. Slant tubes in the autoclave. Close the autoclave door loosely. Autoclave for 10 min at 0 psi pressure– 100°C. Close the autoclave door tightly. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of Corynebacterium diphtheriae. For demonstration of pigment production and proteolysis by Corynebacterium diphtheriae. For the cultivation and maintenance of Moraxella lacunata.
Loeffler Slant Composition per liter: Tryptose ..............................................................5.0g Glucose ...............................................................1.0g Beef serum .................................................. 750.0mL
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into screw-capped tubes. Slant tubes in the autoclave. Close the autoclave door loosely. Autoclave for 10 min at 0 psi pressure– 100°C. Close the autoclave door tightly. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of Corynebacterium diphtheriae. For demonstration of pigment production and proteolysis by Corynebacterium diphtheriae. For the cultivation and maintenance of Moraxella lacunata.
Loeffler Slant, Modified Composition per liter: Glucose ...............................................................1.0g Peptone ...............................................................0.5g Beef serum .................................................. 300.0mL pH 7.6 ± 0.2 at 25°C
Use: For the cultivation of Corynebacterium diph-
Preparation of Medium: Add peptone and glu-
theriae. For demonstration of pigment production and proteolysis by Corynebacterium diphtheriae.
cose to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Add beef serum. Mix thoroughly. Adjust pH to 7.6. Distribute into screw-capped tubes in 3.0mL volumes. Slant tubes in the autoclave. Autoclave for 30 min at 0 psi pressure–100°C.
Loeffler Medium Composition per liter: Beef serum ........................................................70.0g Egg, dried............................................................7.5g Heart muscle, solids from infusion ...................0.72g Glucose .............................................................0.71g
Use: For the cultivation of Corynebacterium diphtheriae. For demonstration of pigment production and proteolysis by Corynebacterium diphtheriae. For the cultivation and maintenance of Moraxella lacunata.
286
Lombard–Dowell Agar
Lombard–Dowell Agar (LD Agar) Agar ..................................................................20.0g Pancreatic digest of casein..................................5.0g Yeast extract........................................................5.0g NaCl ....................................................................2.5g L-Cystine .............................................................0.4g L-Tryptophan .......................................................0.2g Na2SO3 ................................................................0.1g Hemin.............................................................10.0mg NaOH (1N)...................................................... 5.0mL Vitamin K1 solution......................................... 1.0mL pH 7.5 ± 0.2 at 25°C
Vitamin K1 Solution: Composition per 100.0mL: Vitamin K1 ..........................................................1.0g Ethanol .......................................................... 99.0mL
Preparation of Vitamin K1 Solution: Add vitamin K1 to 99.0mL of absolute ethanol. Mix thoroughly.
Preparation of Medium: Add hemin and L-cystine to 5.0mL of NaOH. Mix thoroughly. Add remaining components. Bring volume to 1.0L with distilled/deionized water. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure– 121°C. Pour into sterile Petri dishes.
Use: For the cultivation and identification of a variety of obligate anaerobic bacteria. For the cultivation of Bacteroides species, Fusobacterium species, Clostridium species, and nonspore-forming Gram-positive anaerobes.
Lombard-Dowell Bile Agar (LD Bile Agar) Composition per liter: Agar ..................................................................20.0g Oxgall................................................................20.0g Pancreatic digest of casein..................................5.0g Yeast extract........................................................5.0g NaCl ....................................................................2.5g D-Glucose ............................................................1.0g L-Cystine .............................................................0.4g L-Tryptophan .......................................................0.2g Na2SO3 ................................................................0.1g Hemin.............................................................10.0mg NaOH (1N)...................................................... 5.0mL Vitamin K1 solution ........................................ 1.0mL pH 7.5 ± 0.2 at 25°C
Vitamin K1 Solution: Composition per 100.0mL: Vitamin K1 ..........................................................1.0g Ethanol.......................................................... 99.0mL
Preparation of Vitamin K1 Solution: Add vitamin K1 to 99.0mL of absolute ethanol. Mix thoroughly.
Preparation of Medium: Add hemin and L-cystine to 5.0mL of NaOH. Mix thoroughly. Add remaining components. Bring volume to 1.0L with distilled/deionized water. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure– 121°C. Pour into sterile Petri dishes.
Use: For the cultivation and identification of a variety of obligate anaerobic bacteria in the presence of 20% bile.
Lombard-Dowell Broth (LD Broth) Composition per liter: Pancreatic digest of casein..................................5.0g Yeast extract........................................................5.0g NaCl....................................................................2.5g Agar ....................................................................0.7g L-Tryptophan.......................................................0.2g Na2SO3 ................................................................0.1g NaOH (1N)...................................................... 5.0mL Hemin solution................................................ 1.0mL Vitamin K1 solution ........................................ 1.0mL pH 7.5 ± 0.2 at 25°C
Hemin Solution: Composition per 100.0mL: Hemin .................................................................1.0g NaOH (1N solution)...................................... 20.0mL
Preparation of Hemin Solution: Add hemin to 20.0mL of 1N NaOH solution. Mix thoroughly. Bring volume to 100.0mL with distilled/deionized water.
Vitamin K1 Solution: Composition per 100.0mL: Vitamin K1 ..........................................................1.0g Ethanol.......................................................... 99.0mL
Preparation of Vitamin K1 Solution: Add vitamin K1 to 99.0mL of absolute ethanol. Mix thoroughly.
Preparation of Medium: Add tryptophan to 5.0mL of NaOH. Mix thoroughly. Add remaining components. Bring volume to 1.0L with distilled/deionized water. Mix thoroughly. Gently heat and bring to boiling. Adjust pH to 7.5. Distribute into screw-capped tubes in 7.0mL volumes. Autoclave for 15 min at 15 psi pres-
Lombard-Dowell Gelatin Agar sure–121°C. Cool tubes, with caps loose, under 85% N2 + 10% H2 + 5% CO2. Tighten caps.
Use: For the cultivation of a wide variety of anaerobic bacteria.
Lombard-Dowell Egg Yolk Agar (LD Egg Yolk Agar) (Egg Yolk Agar, Lombard-Dowell)
287
Use: For the cultivation of a wide variety of anaerobic bacteria. For the differentiation of anaerobic bacteria based on lecithinase production, lipase production, and proteolytic ability. Bacteria that produce lecithinase appear as colonies surrounded by a zone of insoluble precipitate. Bacteria that produce lipase appear as colonies with a pearly iridescent sheen. Bacteria that produce proteolytic activity appear as colonies surrounded by a clear zone.
Composition per 9100.0mL: Na2HPO4·12H2O.................................................5.0g Glucose ...............................................................2.0g LD Agar .................................................... 9000.0mL Egg yolk emulsion ...................................... 100.0mL MgSO4·7H20 (5% solution) ............................ 0.2mL pH 7.5 ± 0.2 at 25°C
LD Agar: Composition per liter: Agar ..................................................................20.0g Pancreatic digest of casein..................................5.0g Yeast extract........................................................5.0g NaCl ....................................................................2.5g L-Cystine .............................................................0.4g L-Tryptophan .......................................................0.2g Na2SO3 ................................................................0.1g Hemin.............................................................10.0mg NaOH (1N NaOH) .......................................... 5.0mL Vitamin K1 solution......................................... 1.0mL
Preparation of LD Agar: Add hemin and L-cystine to 5.0mL of NaOH. Mix thoroughly. Add remaining components. Mix thoroughly. Gently heat and bring to boiling.
Vitamin K1 Solution: Composition per 100.0mL: Vitamin K1 ..........................................................1.0g Ethanol .......................................................... 99.0mL
Preparation of Vitamin K1 Solution: Add vitamin K1 to 99.0mL of absolute ethanol. Mix thoroughly.
Egg Yolk Emulsion: Composition: Chicken egg yolks..................................................11 Whole chicken egg...................................................1
Preparation of Egg Yolk Emulsion: Soak eggs with 1:100 dilution of saturated mercuric chloride solution for 1 min. Crack eggs and separate yolks from whites. Mix egg yolks with 1 chicken egg.
Preparation of Medium: Combine components, except egg yolk emulsion. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°– 50°C. Aseptically add 100.0mL of egg yolk emulsion. Mix thoroughly. Pour into sterile Petri dishes.
Lombard-Dowell Esculin Agar (LD Esculin Agar) (Esculin Agar, Lombard-Dowell) Composition per liter: Agar ..................................................................20.0g Pancreatic digest of casein..................................5.0g Yeast extract........................................................5.0g NaCl....................................................................2.5g Esculin ................................................................1.0g Ferric citrate........................................................0.5g L-Cystine .............................................................0.4g L-Tryptophan.......................................................0.2g Hemin ............................................................10.0mg NaOH (1N)...................................................... 5.0mL Vitamin K1 solution......................................... 1.0mL pH 7.5 ± 0.2 at 25°C
Vitamin K1 Solution: Composition per 100.0mL: Vitamin K1 ..........................................................1.0g Ethanol.......................................................... 99.0mL
Preparation of Vitamin K1 Solution: Add vitamin K1 to 99.0mL of absolute ethanol. Mix thoroughly.
Preparation of Medium: Add hemin and L-cystine to 5.0mL of NaOH. Mix thoroughly. Add remaining components. Bring volume to 1.0L with distilled/deionized water. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure– 121°C. Pour into sterile Petri dishes.
Use: For the cultivation of a wide variety of anaerobic bacteria. For the differentiation of anaerobic bacteria based on esculin hydrolysis, H2S production, and catalase production. Bacteria that hydrolyze esculin appear as colonies surrounded by a red-brown to dark brown zone. Bacteria that produce H2S appear as black colonies.
Lombard-Dowell Gelatin Agar (LD Gelatin Agar) Composition per liter: Agar ..................................................................20.0g
288
Lombard-Dowell Neomycin Agar
Pancreatic digest of casein..................................5.0g Yeast extract........................................................5.0g Gelatin.................................................................4.0g NaCl ....................................................................2.5g Glucose ...............................................................1.0g L-Cystine .............................................................0.4g L-Tryptophan .......................................................0.2g Na2SO3 ................................................................0.1g Hemin.............................................................10.0mg NaOH (1N)...................................................... 5.0mL Vitamin K1 solution......................................... 1.0mL pH 7.5 ± 0.2 at 25°C
Vitamin K1 Solution: Composition per 100.0mL: Vitamin K1 ..........................................................1.0g Ethanol .......................................................... 99.0mL
Preparation of Vitamin K1 Solution: Add vitamin K1 to 99.0mL of absolute ethanol. Mix thoroughly.
Preparation of Medium: Add hemin and L-cystine to 5.0mL of NaOH. Mix thoroughly. Add remaining components, except agar and gelatin. Bring volume to 750.0mL with distilled/deionized water. Mix thoroughly. Gently heat and bring to boiling. In a separate flask, add gelatin to 100.0mL of cold distilled/deionized water. Gently heat and bring to 70°C. Add gelatin solution to the 750.0mL of basal medium. Mix thoroughly. Add agar. Bring volume to 1.0L with distilled/deionized water. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes.
Use: For the cultivation of a wide variety of anaerobic bacteria. For the differentiation of anaerobic bacteria based on gelatinase production. After incubation of plates, gelatinase activity is determined by the addition of Frazier’s reagent. Bacteria that hydrolyze gelatin appear as colonies surrounded by a clear zone.
Lombard-Dowell Neomycin Agar (Egg Yolk Agar with Neomycin) Composition per 9100.0mL: Na2HPO4·12H2O.................................................5.0g Glucose ...............................................................2.0g Neomycin sulfate ................................................0.1g LD Agar .................................................... 9000.0mL Egg yolk emulsion ...................................... 100.0mL MgSO4·7H20 (5% solution) ............................ 0.2mL pH 7.5 ± 0.2 at 25°C
LD Agar: Composition per liter: Agar ..................................................................20.0g Pancreatic digest of casein..................................5.0g Yeast extract........................................................5.0g
NaCl....................................................................2.5g L-Cystine .............................................................0.4g L-Tryptophan.......................................................0.2g Na2SO3 ................................................................0.1g Hemin ............................................................10.0mg NaOH (1N NaOH) .......................................... 5.0mL Vitamin K1 solution......................................... 1.0mL
Preparation of LD Agar: Add hemin and L-cystine to 5.0mL of NaOH. Mix thoroughly. Add remaining components. Mix thoroughly. Gently heat and bring to boiling.
Vitamin K1 Solution: Composition per 100.0mL: Vitamin K1 ..........................................................1.0g Ethanol.......................................................... 99.0mL
Preparation of Vitamin K1 Solution: Add vitamin K1 to 99.0mL of absolute ethanol. Mix thoroughly.
Egg Yolk Emulsion: Composition: Chicken egg yolks.................................................. 11 Whole chicken egg ..................................................1
Preparation of Egg Yolk Emulsion: Soak eggs with 1:100 dilution of saturated mercuric chloride solution for 1 min. Crack eggs and separate yolks from whites. Mix egg yolks with 1 chicken egg.
Preparation of Medium: Combine components, except egg yolk emulsion and neomycin sulfate. Mix thoroughly. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C. Aseptically add 100.0mL of egg yolk emulsion and neomycin sulfate. Mix thoroughly. Pour into sterile Petri dishes.
Use: For the selective cultivation of a wide variety of anaerobic bacteria. For the differentiation of anaerobic bacteria based on lecithinase production, lipase production, and proteolytic ability. Bacteria that produce lecithinase appear as colonies surrounded by a zone of insoluble precipitate. Bacteria that produce lipase appear as colonies with a pearly iridescent sheen. Bacteria that produce proteolytic activity appear as colonies surrounded by a clear zone.
Long-Term Preservation Medium Composition per liter: NaCl..................................................................30.0g Peptone .............................................................10.0g Agar ....................................................................3.0g Yeast extract........................................................3.0g
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into screw-capped tubes in 4.0mL vol-
Low Iron YC Broth
289
umes. Autoclave for 15 min at 15 psi pressure– 121°C.
100.0mL. Mix thoroughly. Autoclave for 10 min at 11 psi pressure–116°C. Cool to 45°–50°C.
Use: For the cultivation and maintenance of a wide
Preparation of Medium: To 1.0L of solution 1,
variety of bacteria.
Low Iron YC Agar Composition per 1033.0mL: Solution 1........................................................... 1.0L Solution 4...................................................... 30.0mL Solution 2........................................................ 2.0mL Solution 3........................................................ 1.0mL pH 7.4 ± 0.2 at 25°C
Solution 1: Composition per liter: Yeast extract......................................................20.0g Noble agar.........................................................10.0g Casamino acids .................................................10.0g KH2PO4 ...............................................................5.0g CaCl2 ...................................................................1.0g Tryptophan ........................................................0.05g
Preparation of Solution 1: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.4. Gently heat and bring to boiling. Filter through no. 40 ashless filter paper. Solution 2: Composition per 100.0mL: MgSO4·7H2O ....................................................22.5g CuSO4·5H2O .......................................................0.5g ZnSO4·5H2O .......................................................0.2g β-Alanine ........................................................0.115g Nicotinic acid ..................................................0.115g MnCl2·4H2O ...................................................0.075g Pimelic acid......................................................7.5mg HCl, concentrated ........................................... 3.0mL
Preparation of Solution 2: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Solution 3: Composition per 100.0mL: L-Cystine ...........................................................20.0g
HCl, concentrated ......................................... 20.0mL
Preparation of Solution 3: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Solution 4: Composition per 100.0mL: Maltose..............................................................50.0g CaCl2·2H2O.........................................................0.5g
Preparation of Solution 4: Add components to distilled/deionized water and bring volume to
add 2.0mL of solution 2 and 1.0mL of solution 3. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 30.0mL of sterile solution 4. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation and maintenance of Corynebacterium diphtheriae.
Low Iron YC Broth Composition per 1033.0mL: Solution 1........................................................... 1.0L Solution 4...................................................... 30.0mL Solution 2........................................................ 2.0mL Solution 3........................................................ 1.0mL pH 7.4 ± 0.2 at 25°C
Solution 1: Composition per liter: Yeast extract......................................................20.0g Casamino acids .................................................10.0g KH2PO4...............................................................5.0g CaCl2·2H2O ........................................................1.0g Tryptophan........................................................0.05g
Preparation of Solution 1: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.4. Gently heat and bring to boiling. Filter through #40 ashless filter paper.
Solution 2: Composition per 100.0mL: MgSO4·7H2O ....................................................22.5g CuSO4·5H2O .......................................................0.5g ZnSO4·5H2O .......................................................0.2g β-Alanine ........................................................ 0.115g Nicotinic acid.................................................. 0.115g MnCl2·4H2O ...................................................0.075g Pimelic acid .....................................................7.5mg HCl, concentrated ........................................... 3.0mL
Preparation of Solution 2: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Solution 3: Composition per 100.0mL: L-Cystine ...........................................................20.0g
HCl, concentrated ......................................... 20.0mL
Preparation of Solution 3: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly.
290
Lowenstein-Gruft Medium
Solution 4: Composition per 100.0mL: Maltose..............................................................50.0g CaCl2·2H2O.........................................................0.5g
Preparation of Solution 4: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Autoclave for 10 min at 11 psi pressure–116°C. Cool to 25°C. Preparation of Medium: To 1.0L of solution 1, add 2.0mL of solution 2 and 1.0mL of solution 3. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C. Aseptically add 30.0mL of sterile solution 4. Mix thoroughly. Aseptically distribute into sterile tubes or flasks. Use: For the cultivation and maintenance of Corynebacterium diphtheriae.
Lowenstein-Gruft Medium Composition per 1600.0mL: Potato starch......................................................30.0g Asparagine ..........................................................3.6g KH2PO4 ...............................................................2.4g Magnesium citrate...............................................0.6g Malachite Green..................................................0.4g MgSO4·7H2O ....................................................0.24g Nalidixic acid ..................................................0.056g Ribonucleic acid ............................................0.08mg Homogenized whole egg .................................. 1.0L Glycerol ........................................................ 12.0mL Penicillin ......................................................80,000U
Homogenized Whole Egg: Composition per liter: Whole eggs ......................................................18–24
Use: For the cultivation and differentiation of Mycobacterium species. Mycobacterium tuberculosis appears as granular, rough, dry colonies. Mycobacterium kansasii appears as smooth to rough photochromogenic colonies. Mycobacterium gordonae appears as smooth yellow-orange colonies. Mycobacterium avium appears as smooth, colorless colonies. Mycobacterium smegmatis appears as wrinkled, creamy white colonies.
Lowenstein-Jensen Medium Composition per 1600.0mL: Potato starch......................................................30.0g Asparagine ..........................................................3.6g KH2PO4...............................................................2.4g Magnesium citrate ..............................................0.6g Malachite Green..................................................0.4g MgSO4·7H2O ....................................................0.24g Homogenized whole egg .................................. 1.0L Glycerol ........................................................ 12.0mL
Source: This medium is available as a prepared medium from BD Diagnostic Systems and Oxoid Unipath.
Homogenized Whole Egg: Composition per liter: Whole eggs ...................................................... 18-24
Preparation of Homogenized Whole Egg: Use fresh eggs, less than 1 week old. Scrub the shells with soap. Let stand in a soap solution for 30 min. Rinse in running water. Soak eggs in 70% ethanol for 15 min. Break the eggs into a sterile container. Homogenize by shaking. Filter through four layers of sterile cheesecloth into a sterile graduated cylinder. Measure out 1.0L.
Preparation of Medium: Add glycerol to
Preparation of Medium: Add glycerol to 600.0mL of distilled/deionized water. Mix thoroughly. Add remaining components, except fresh egg mixture. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 50°C. Aseptically add 1.0L of homogenized whole egg. Mix thoroughly. Distribute into sterile screw-capped tubes. Place tubes in a slanted position. Inspissate at 85°C (moist heat) for 45 min.
600.0mL of distilled/deionized water. Mix thoroughly. Add remaining components, except fresh egg mixture. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C. Aseptically add 1.0L of homogenized whole egg. Mix thoroughly. Distribute into sterile screw-capped tubes. Place tubes in a slanted position. Inspissate at 85°C (moist heat) for 45 min.
bacterium species. Mycobacterium tuberculosis appears as granular, rough, dry colonies. Mycobacterium kansasii appears as smooth to rough photochromogenic colonies. Mycobacterium gordonae appears as smooth yellow-orange colonies. Mycobacterium avium appears as smooth, colorless colonies. Mycobacterium smegmatis appears as wrinkled, creamy white colonies. Also used for the cultivation and mainte-
Preparation of Homogenized Whole Egg: Use fresh eggs, less than 1 week old. Scrub the shells with soap. Let stand in a soap solution for 30 min. Rinse in running water. Soak eggs in 70% ethanol for 15 min. Break the eggs into a sterile container. Homogenize by shaking. Filter through four layers of sterile cheesecloth into a sterile graduated cylinder. Measure out 1.0L.
Use: For the cultivation and differentiation of Myco-
LPM Agar nance of Gordona species, Nocardia species, Rhodococcus species, and Tsukamurella paurometabolum.
Lowenstein-Jensen Medium without Glycerol Composition per 1600mL: Potato starch......................................................30.0g Asparagine ..........................................................3.6g KH2PO4 ...............................................................2.4g Magnesium citrate...............................................0.6g Malachite green...................................................0.4g MgSO4·7H2O ....................................................0.24g Homogenized whole egg .................................. 1.0L
Homogenized Whole Egg: Composition per liter: Whole eggs ......................................................18–24
Preparation of Homogenized Whole Egg: Use fresh eggs, less than 1 week old. Scrub the shells with soap. Let stand in a soap solution for 30 min. Rinse in running water. Soak eggs in 70% ethanol for 15 min. Break the eggs into a sterile container. Homogenize by shaking. Filter through four layers of sterile cheesecloth into a sterile graduated cylinder. Measure out 1.0L.
Preparation of Medium: Add components, except fresh egg mixture, to 600.0mL of distilled/ deionized water. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C. Aseptically add 1.0L of homogenized whole egg. Mix thoroughly. Distribute into sterile screw-capped tubes. Place tubes in a slanted position. Inspissate at 85°C (moist heat) for 45 min.
Use: For the cultivation and maintenance of Mycobacterium species, especially Mycobacterium bovis and other species that are sensitive to glycerol.
Lowenstein-Jensen Medium with Streptomycin Composition per 1610.0mL: Potato starch......................................................30.0g Asparagine ..........................................................3.6g KH2PO4 ...............................................................2.4g Magnesium citrate...............................................0.6g Malachite Green..................................................0.4g MgSO4·7H2O ....................................................0.24g Homogenized whole egg .................................. 1.0L Glycerol ........................................................ 12.0mL Streptomycin solution ................................... 10.0mL
Homogenized Whole Egg: Composition per liter: Whole eggs ...................................................... 18-24
291
Preparation of Homogenized Whole Egg: Use fresh eggs, less than 1 week old. Scrub the shells with soap. Let stand in a soap solution for 30 min. Rinse in running water. Soak eggs in 70% ethanol for 15 min. Break the eggs into a sterile container. Homogenize by shaking. Filter through four layers of sterile cheesecloth into a sterile graduated cylinder. Measure out 1.0L.
Streptomycin Solution: Composition per 10.0mL: Streptomycin....................................................0.1mg
Preparation of Streptomycin Solution: Add streptomycin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. Preparation of Medium: Add glycerol to 600.0mL of distilled/deionized water. Mix thoroughly. Add remaining components, except fresh egg mixture and streptomycin solution. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C. Aseptically add 1.0L of homogenized whole egg and 10.0mL of sterile streptomycin solution. Mix thoroughly. Distribute into sterile screw-capped tubes. Place tubes in a slanted position. Inspissate at 85°C (moist heat) for 45 min.
Use: For the cultivation and differentiation of Mycobacterium species. Mycobacterium tuberculosis appears as granular, rough, dry colonies. Mycobacterium kansasii appears as smooth to rough photochromogenic colonies. Mycobacterium gordonae appears as smooth yellow-orange colonies. Mycobacterium avium appears as smooth, colorless colonies. Mycobacterium smegmatis appears as wrinkled, creamy white colonies. Also used for the cultivation and maintenance of Gordona species, Nocardia species, Rhodococcus species, and Tsukamurella paurometabolum.
LPM Agar (Lithium Chloride Phenylethanol Moxalactam Plating Agar) Composition per liter: Agar ..................................................................15.0g Glycine anhydride.............................................10.0g LiCl .....................................................................5.0g NaCl....................................................................5.0g Pancreatic digest of casein..................................5.0g Peptic digest of animal tissue .............................5.0g Beef extract.........................................................3.0g Phenylethyl alcohol ............................................2.5g Moxalactam solution ...................................... 2.0mL pH 7.3 ± 0.2 at 25°C
292
LPM Agar with Esculin and Ferric Iron
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Moxalactam Solution: Composition per 10.0mL: Moxalactam ........................................................0.1g
Preparation of Moxalactam Solution: Add moxalactam to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. Preparation of Medium: Add components, except moxalactam solution, to distilled/deionized water and bring volume to 998.0mL. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 12 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 2.0mL of sterile moxalactam solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation and cultivation of Listeria monocytogenes.
LPM Agar with Esculin and Ferric Iron Composition per liter: Agar ..................................................................15.0g Glycine anhydride.............................................10.0g LiCl .....................................................................5.0g NaCl ....................................................................5.0g Pancreatic digest of casein..................................5.0g Peptic digest of animal tissue..............................5.0g Beef extract .........................................................3.0g Phenylethyl alcohol.............................................2.5g Esculin ................................................................1.0g Ferric ammonium citrate.....................................0.5g Moxalactam solution....................................... 2.0mL pH 7.3 ± 0.2 at 25°C
Moxalactam Solution: Composition per 10.0mL: Moxalactam ........................................................0.1g
Preparation of Moxalactam Solution: Add moxalactam to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. Preparation of Medium: Add components, except moxalactam solution, to distilled/deionized water and bring volume to 998.0mL. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 12 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 2.0mL of sterile moxalactam solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation and cultivation of Listeria monocytogenes.
LST-MUG Broth Composition per liter: Tryptose ............................................................20.0g Lactose................................................................5.0g NaCl....................................................................5.0g K2HPO4 ............................................................2.75g KH2PO4 ............................................................2.75g L-Tryptophan ......................................................1.0g Sodium lauryl sulfate..........................................0.1g 4-Methylumbelliferyl-β-D-glucuronide ..............0.1g pH 6.8 ± 0.2 at 37°C
Source: This medium is available from Fluka, Sigma-Aldrich.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into test tubes that contain an inverted Durham tube in 10.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the detection of E. coli by the fluorgenic method. The presence of E. coli results in fluorescence in the UV. A positive indole test provide confirmation. β-D-glucoronidase, which is produced by E. coli, cleaves 4-methylumbelliferyl-β-D-glucuronide to 4-methylumbelliferone and glucuronide. The fluorogen 4-methylumbelliferone can be detected under a long wavelength UV lamp.
Lysine Arginine Iron Agar Composition per liter: Agar ..................................................................15.0g L-Arginine .........................................................10.0g L-Lysine.............................................................10.0g Peptone ...............................................................5.0g Yeast extract........................................................3.0g Glucose ...............................................................1.0g Ferric ammonium citrate.....................................0.5g Sodium thiosulfate ............................................0.04g Bromcresol Purple ............................................0.02g pH 6.8 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Adjust pH to 6.8. Distribute into screw-capped tubes in 5.0mL volumes. Autoclave for 12 min at 15 psi pressure– 121°C. Allow tubes to cool in a slanted position.
Use: For the cultivation and differentiation of bacteria based on their ability to decarboxylate lysine, decarboxylate arginine, and produce H2S. Bacteria that decarboxylate lysine or arginine turn the medium purple. Bacteria that produce H2S appear as black colonies.
Lysine Iron Agar
Lysine Broth Falkow with NaCl Composition per liter: L-Lysine
..............................................................5.0g Peptone or gelysate .............................................5.0g Yeast extract........................................................3.0g Glucose ...............................................................1.0g Bromcresol Purple ............................................0.02g pH 6.5 ± 0.2 at 25°C
293
Mix thoroughly. Gently heat and bring to boiling. Adjust pH to 6.1. Distribute into tubes in 5.0mL volumes. Autoclave for 15 min at 15 psi pressure– 121°C.
Use: For the cultivation and differentiation of bacteria, especially Salmonella, based on their ability to decarboxylate lysine. Bacteria that decarboxylate lysine turn the medium turbid purple.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH so that it will be 6.5 ± 0.2 after sterilization. Distribute into 16 × 150mm screwcapped tubes in 5.0mL volumes. Autoclave medium with loosely capped tubes for 10 min at 15 psi pressure– 121°C. Screw the caps on tightly for storage and after inoculation.
Use: For the cultivation and differentiation of Vibrio spp. based on their ability to decarboxylate the amino acid lysine. Bacteria that decarboxylate lysine turn the medium turbid purple.
Lysine Decarboxylase Broth, Taylor Modification (Lysine Decarboxylase Broth) Composition per liter: L-Lysine...............................................................5.0g
Peptone ...............................................................5.0g Yeast extract........................................................3.0g Glucose ...............................................................1.0g Bromcresol Purple ............................................0.02g pH 6.8 ± 0.2 at 25°C
Source: This medium is available as a premixed
Lysine Decarboxylase Broth, Falkow
powder from BD Diagnostic Systems.
Composition per liter:
Preparation of Medium: Add components to
Peptone................................................................5.0g L-Lysine...............................................................5.0g Yeast extract........................................................3.0g Glucose ...............................................................1.0g Bromcresol Purple ............................................0.02g pH 6.5–6.8 at 25°C
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Adjust pH to 6.1. Distribute into tubes in 5.0mL volumes. Autoclave for 15 min at 15 psi pressure– 121°C.
Preparation of Medium: Add components to
ria, especially Salmonella, based on their ability to decarboxylate lysine. Bacteria that decarboxylate lysine turn the medium turbid purple.
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Adjust pH to 6.5–6.8. Distribute into tubes in 5.0mL volumes. Autoclave for 15 min at 15 psi pressure– 121°C.
Use: For the cultivation and differentiation of bacteria, especially Salmonella, based on their ability to decarboxylate lysine. Bacteria that decarboxylate lysine turn the medium turbid purple.
Use: For the cultivation and differentiation of bacte-
Lysine Decarboxylase Medium Composition per liter: Glucose ...............................................................0.5g KH2PO4...............................................................0.5g L-Lysine·HCl .......................................................0.5g pH 4.6 ± 0.2 at 25°C
Preparation of Medium: Add components to
Lysine Decarboxylase Broth, Taylor Modification Composition per liter: L-Lysine...............................................................5.0g
Yeast extract........................................................3.0g Glucose ...............................................................1.0g Bromcresol Purple ............................................0.02g pH 6.1 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath.
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Adjust pH to 4.6. Autoclave for 15 min at 15 psi pressure–121°C. Aseptically distribute into sterile tubes in 1.0mL volumes.
Use: For the cultivation and differentiation of Gramnegative, nonfermentative bacteria based on their ability to decarboxylate lysine. Bacteria that decarboxylate lysine turn the medium turbid purple.
Lysine Iron Agar
Preparation of Medium: Add components to
Composition per liter:
distilled/deionized water and bring volume to 1.0L.
Agar ..................................................................13.5g
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Lysine Ornithine Mannitol Agar
L-Lysine.............................................................10.0g
Pancreatic digest of gelatin .................................5.0g Yeast extract........................................................3.0g Glucose ...............................................................1.0g Ferric ammonium citrate.....................................0.5g Na2S2O3·5H2O ..................................................0.04g Bromcresol Purple ............................................0.02g pH 6.7 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems and Oxoid Unipath. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Distribute into tubes in 10.0mL volumes. Autoclave for 12 min at 15 psi pressure–121°C. Allow tubes to cool in a slanted position.
Use: For the cultivation and differentiation of members of the Enterobacteriaceae based on their ability to decarboxylate lysine and to form H2S. Bacteria that decarboxylate lysine turn the medium purple. Bacteria that produce H2S appear as black colonies.
Lysine Ornithine Mannitol Agar (LOM Agar) Composition per liter: Agar ..................................................................13.5g L–Ornithine·HCl .................................................6.5g D–Mannitol .......................................................5.25g L–Lysine·HCl ......................................................5.0g NaCl ....................................................................5.0g Yeast extract........................................................3.0g Bromthymol Blue ...............................................0.3g Vancomycin solution..................................... 10.0mL pH 6.5 ± 0.2 at 25°C
Vancomycin Solution: Composition per 10.0mL: Vancomycin·HCl...............................................0.03g
Preparation of Vancomycin Solution: Add vancomycin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except vancomycin solution, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile vancomycin solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation and differentiation of Gramnegative bacilli based on their ability to decarboxylate lysine or ornithine and mannitol fermentation.
Especially useful for the identification of Enterobacter agglomerans. Bacteria that ferment mannitol appear as dark yellow colonies. Bacteria that decarboxylate lysine or ornithine appear as green-yellow colonies.
M7 Medium Composition per liter: Yeast extract solution.................................. 200.0mL Dialyzed fetal bovine serum ....................... 100.0mL L-Methionine solution................................... 30.0mL Buffer solution .............................................. 20.0mL Glucose solution ........................................... 20.0mL
Yeast Extract Solution: Composition per liter: Yeast extract......................................................25.0g
Preparation of Yeast Extract Solution: Add yeast extract to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C. L-Methionine
Solution: Composition per liter: L-Methionine.......................................................1.5g
Preparation of L-Methionine Solution: Add Lmethionine to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C. Glucose Solution: Composition per liter: Glucose ...........................................................270.0g
Preparation of Glucose Solution: Add glucose to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C.
Buffer Solution: Composition per liter: Na2HPO4 .......................................................... 25.0g KH2PO4.............................................................18.1g
Preparation of Buffer Solution: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C.
Dialyzed Fetal Bovine Serum: Composition per 100.0mL: Fetal bovine serum, heat inactivated .......... 100.0mL
Preparation of Dialyzed Fetal Bovine Serum: Dialyze the heat-inactivated serum at 0°–4°C against 10 volumes of water. Clean the dialysis tubing before use by boiling in a solution of 0.37g/L of EDTA and rinsing with water. Change the water four times at
MacConkey Agar 8–16 hr intervals. Centrifuge the dialyzed serum for 30 min at 35,000 x g. Filter sterilize serum fluid.
Preparation of Medium: Aseptically combine the sterile solutions. Mix thoroughly. Bring volume to 1.0L with sterile distilled/deionized water. Use: For the cultivation of Naegleria fowleri, Naegleria gruberi, and Nuclearia species.
M9 Medium with Casamino Acids Composition per liter: Na2HPO4 .............................................................6.0g Casamino acids ...................................................5.0g KH2PO4 ...............................................................3.0g NH4Cl .................................................................1.0g NaCl ....................................................................0.5g Glucose solution ........................................... 10.0mL MgSO4·7H2O solution .................................... 1.0mL Thiamine·HCl solution.................................... 1.0mL CaCl2 solution ................................................. 1.0mL pH 7.0 ± 0.2 at 25°C
Glucose solution: Composition per 100.0mL: D-Glucose ..........................................................20.0g
Preparation of Glucose Solution: Add glucose to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C.
295
mine·HCl solution, and CaCl2 solution, to distilled/ deionized water and bring volume to 987.0mL. Mix thoroughly. Adjust pH to 7.0. Autoclave for 15 min at 15 psi pressure–121°C. Cool to room temperature. Aseptically add sterile MgSO4·7H2O solution, sterile glucose solution, sterile thiamine·HCl solution, and sterile CaCl2 solution. Mix thoroughly. Distribute into tubes or flasks.
Use: For the cultivation and maintenance of Flavobacterium meningosepticum.
MacConkey Agar Composition per liter: Pancreatic digest of gelatin...............................17.0g Agar ..................................................................13.5g Lactose..............................................................10.0g NaCl....................................................................5.0g Bile salts..............................................................1.5g Pancreatic digest of casein..................................1.5g Peptic digest of animal tissue .............................1.5g Neutral Red.......................................................0.03g Crystal Violet ...................................................1.0mg pH 7.1 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to
MgSO4·7H2O Solution: Composition per liter:
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring until boiling. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or distribute into sterile tubes.
MgSO4·7H2O ..................................................246.5g
Use: For the selective isolation, cultivation, and dif-
Preparation of MgSO4·7H2O Solution: Add MgSO4·7H2O to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C.
ferentiation of coliforms and enteric pathogens based on the ability to ferment lactose. Lactose-fermenting organisms appear as red to pink colonies. Lactosenonfermenting organisms appear as colorless or transparent colonies.
Thiamine·HCl Solution: Composition per 10.0mL: Thiamine·HCl ................................................10.0mg
Preparation of Thiamine·HCl Solution: Add thiamine·HCl to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
CaCl2 Solution: Composition per liter: CaCl2 solution ...................................................14.7g
Preparation of CaCl2 Solution: Add CaCl2 so-
MacConkey Agar Composition per liter: Peptone .............................................................20.0g Agar ..................................................................12.0g Lactose..............................................................10.0g Bile salts..............................................................5.0g NaCl....................................................................5.0g Neutral Red.....................................................0.075g pH 7.4 ± 0.2 at 25°C
lution to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C.
Source: This medium is available as a premixed
Preparation of Medium: Add components, ex-
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring until boil-
cept MgSO4·7H2O solution, glucose solution, thia-
powder from Oxoid Unipath.
Preparation of Medium: Add components to
296
MacConkey Agar, CS
ing. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the selective isolation, cultivation, and differentiation of coliforms and enteric pathogens based on the ability to ferment lactose. Lactose-fermenting organisms appear as red to pink colonies. Lactosenonfermenting organisms appear as colorless or transparent colonies.
MacConkey Agar, CS Composition per liter:
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring until boiling. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the selective isolation, cultivation, and differentiation of enteric pathogens, especially enterococci, in clinical specimens and in materials of sanitary importance.
MacConkey Agar No. 3
Peptone..............................................................17.0g Agar ..................................................................13.5g Lactose ..............................................................10.0g NaCl ....................................................................5.0g Proteose peptone .................................................3.0g Bile salts..............................................................1.5g Neutral Red .......................................................0.03g Crystal Violet ...................................................1.0mg pH 7.1 ± 0.2 at 25°C
Composition per liter:
Source: This medium is available as a prepared me-
Source: This medium is available as a premixed
Peptone .............................................................20.0g Agar ..................................................................15.0g Lactose..............................................................10.0g NaCl....................................................................5.0g Bile salts no. 3.....................................................1.5g Neutral Red.......................................................0.03g Crystal Violet ..................................................0.001g pH 7.1 ± 0.2 at 25°C
dium from BD Diagnostic Systems.
powder from Oxoid Unipath.
Preparation of Medium: Add components to
Preparation of Medium: Add components to
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring until boiling. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or distribute into sterile tubes.
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring until boiling. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation and differentiation of lac-
Use: For the selective isolation, cultivation, and dif-
tose-fermenting and nonfermenting Gram-negative bacteria while also controlling the swarming of Proteus species, if present. Lactose-fermenting organisms appear as red to pink colonies. Lactose-nonfermenting organisms appear as colorless or transparent colonies.
MacConkey Agar No. 2 (MacConkey II Agar) Composition per liter: Peptone..............................................................20.0g Agar ..................................................................15.0g Lactose ..............................................................10.0g NaCl ....................................................................5.0g Bile salts no. 2.....................................................1.5g Neutral Red .......................................................0.05g Crystal Violet ...................................................1.0mg pH 7.2 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems and Oxoid Unipath.
ferentiation of enteric pathogens, especially Salmonella and Shigella, in clinical specimens.
MacConkey Agar without Crystal Violet Composition per liter: Agar ..................................................................12.0g Lactose..............................................................10.0g Pancreatic digest of casein................................10.0g Peptic digest of animal tissue ...........................10.0g Bile salts..............................................................5.0g NaCl....................................................................5.0g Neutral Red.......................................................0.05g pH 7.4 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring until boiling. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or distribute into sterile tubes.
Maintenance of L Antigen in Neisseria Use: For the detection of members of the Enterobacteriaceae and enterococci as well as some staphylococci.
MacConkey Agar, Fluorocult (Fluorocult MacConkey Agar) Composition per liter: Peptone from casein..........................................17.0g Agar ..................................................................13.5g Lactose ..............................................................10.0g NaCl ....................................................................5.0g Peptone from meat ..............................................3.0g Bile salt mixture..................................................1.5g 4-Methylumbelliferyl-β-D-glucuronide ..............0.1g Neutral Red .......................................................0.03g Crystal Violet ..................................................0.001g pH 7.1 ± 0.2 at 25°C
Source: This medium is available from Merck. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Pour into sterile Petri dishes. The plates are clear and red to red-brown.
Use: For the isolation of Salmonella, Shigella, and coliform bacteria, in particular E. coli, from various specimens. The bile salts and crystal violet largely inhibit the growth of Gram-positive microbial flora. Lactose together with the pH indicator neutral red are used to detect lactose-positive colonies and E. coli can be seen among these because of fluorescence under UV light.
MacConkey Agar without Salt Composition per liter: Peptone..............................................................20.0g Agar ..................................................................12.0g Lactose ..............................................................10.0g Bile salts..............................................................5.0g Neutral Red .....................................................0.075g pH 7.4 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems and Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring until boiling. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or distribute into sterile tubes. Dry the surface of plates before inoculation.
297
lyte medium on which most Proteus species will not swarm and therefore avoids overgrowth of the plate.
MacConkey MUG Agar Composition per liter: Casein peptone..................................................17.0g Agar ..................................................................13.5g Lactose..............................................................10.0g NaCl....................................................................5.0g Meat peptone ......................................................3.0g Bile salt mixture..................................................1.5g 4-Methylumbelliferyl-β-D-glucuronide ..............0.1g Neutral Red.......................................................0.03g Crystal Violet ..................................................0.001g pH 7.1 ± 0.2 at 37°C
Source: This medium is available from Fluka, Sigma-Aldrich.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 50°C. Pour into sterile Petri dishes.
Use: For the isolation of Salmonella, Shigella, and coliform bacteria, in particular E. coli, from diverse specimens. Bile salts and crystal violet extensively inhibit the Gram-positive flora. The presence of lactose and neutral red indicate lactose-positive colonies from which E. coli can be identified by fluorescence in the UV.
Magnesium Oxalate Agar (MOX Agar) Composition per liter: Pancreatic digest of casein................................15.0g Agar ..................................................................15.0g Papaic digest of soybean meal............................5.0g NaCl....................................................................5.0g MgCl2·6H2O .......................................................4.1g Sodium oxalate .................................................2.68g pH 7.4–7.6 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation of Yersinia enterocolitica.
Maintenance of L Antigen in Neisseria
Use: For the isolation and detection of coliforms and
Composition per liter:
enteric pathogens from urine. Provides a low electro-
Proteose peptone no. 3......................................20.0g
298
Malachite Green Broth
Agar ..................................................................15.0g Na2HPO4 .............................................................5.0g NaCl ....................................................................5.0g Glucose ...............................................................0.5g Rabbit blood, defibrinated .......................... 100.0mL pH 7.4–7.6 at 25°C
Preparation of Medium: Add components, except rabbit blood, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat while stirring until boiling. Autoclave for 20 min at 15 psi pressure–121°C. Cool to 60°C. Aseptically add 100.0mL of sterile, defibrinated rabbit blood. Maintain at 75°C while shaking for 30 min. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation and maintenance of Neisseria gonorrhoeae.
Malachite Green Broth Composition per liter: Peptone..............................................................15.0g Beef extract .........................................................9.0g Malachite Green.............................................0.01mg pH 7.3 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of Pseudomonas aeruginosa.
Malonate Broth Composition per liter: Sodium malonate ................................................3.0g NaCl ....................................................................2.0g (NH4)2SO4...........................................................2.0g K2HPO4 ...............................................................0.6g KH2PO4 ...............................................................0.4g Bromthymol Blue ...........................................0.025g pH 6.7 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Avoid introduction of carbon and nitrogen from other sources.
Use: For the cultivation and differentiation of coliforms and other enteric organisms, particularly Enterobacter and Escherichia, based on their ability to utilize malonate as the sole carbon source and ammonium sulfate as the sole nitrogen source. Malonate-utilizing organisms turn the medium blue.
Malonate Broth, Ewing Modified Composition per liter: Sodium malonate ................................................3.0g NaCl....................................................................2.0g (NH4)2SO4 ..........................................................2.0g Yeast extract........................................................1.0g K2HPO4...............................................................0.6g KH2PO4...............................................................0.4g Glucose .............................................................0.25g Bromthymol Blue ...........................................0.025g pH 6.7 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation and differentiation of coliforms and other enteric organisms, particularly Enterobacter and Escherichia, based on their ability to utilize malonate as a carbon source and ammonium sulfate as a nitrogen source. The small amount of yeast extract and glucose encourages the growth of some organisms that may be distressed or fail to respond. Malonate-utilizing organisms turn the medium blue.
Malt Agar Composition per liter: Agar ..................................................................20.0g Malt extract.......................................................12.5g
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat until boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of fungi.
Mannitol Salt Agar Composition per liter: NaCl..................................................................75.0g Agar ..................................................................15.0g D-Mannitol ........................................................10.0g Pancreatic digest of casein..................................5.0g Peptic digest of animal tissue .............................5.0g Beef extract.........................................................1.0g Phenol Red......................................................0.025g pH 7.4 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems and Oxoid Unipath.
Martin-Lewis Agar, Enriched
299
Preparation of Medium: Add components to
Preparation of VCAT Inhibitor: Add compo-
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
nents to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Use: For the selective isolation, cultivation, and enumeration of staphylococci from clinical and nonclinical specimens. Mannitol-utilizing organisms turn the medium yellow.
Martin-Lewis Agar
Preparation of Medium: Add components, except supplement solution enrichment and VCAT inhibitor, to distilled/deionized water and bring volume to 980.0mL. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C. Aseptically add sterile supplement solution enrichment and sterile VCAT inhibitor. Mix thoroughly. Pour into sterile Petri dishes.
Composition per liter:
Use: For the isolation and cultivation of pathogenic
Agar ..................................................................12.0g Hemoglobin ......................................................10.0g Pancreatic digest of casein..................................7.5g Selected meat peptone ........................................7.5g NaCl ....................................................................5.0g K2HPO4 ...............................................................4.0g Cornstarch...........................................................1.0g KH2PO4 ...............................................................1.0g Supplement solution ..................................... 10.0mL VCAT inhibitor ............................................. 10.0mL pH 7.2 ± 0.22 at 25°C
Neisseria from specimens containing mixed flora of bacteria and fungi.
Source: Martin-Lewis agar is available as a prepared medium from BD Diagnostic Systems.
Supplement Solution: Composition per liter: Glucose ...........................................................100.0g L-Cysteine·HCl..................................................25.9g L-Glutamine.......................................................10.0g L-Cystine .............................................................1.1g Adenine...............................................................1.0g Nicotinamide adenine dinucleotide ..................0.25g Vitamin B12 .........................................................0.1g Thiamine pyrophosphate.....................................0.1g Guanine·HCl .....................................................0.03g Fe(NO3)3·6H2O .................................................0.02g p-Aminobenzoic acid......................................0.013g Thiamine·HCl ..................................................3.0mg
Martin-Lewis Agar, Enriched Composition per liter: Agar ..................................................................12.0g Pancreatic digest of casein..................................7.5g Selected meat peptone ........................................7.5g NaCl....................................................................5.0g K2HPO4...............................................................4.0g Cornstarch...........................................................1.0g KH2PO4...............................................................1.0g Sarcina lutea suspension .............................. 20.0mL Horse serum, inactivated .............................. 20.0mL Supplement solution ..................................... 10.0mL PCAT inhibitor.............................................. 10.0mL pH 7.2 ± 0.22 at 25°C
Source: The supplement solution (IsoVitaleX enrichment) is available from BD Diagnostic Systems. This enrichment may be replaced by supplement VX from BD Diagnostic Systems.
Sarcina lutea Suspension: Composition per 20.0mL: Sarcina lutea FDA 1001 .......................106–107 cells
Preparation of Sarcina lutea Suspension:
Preparation of Supplement Solution: Add
Aseptically wash the growth of 24-h cultures of Sarcina lutea FDA 1001 cells from Thayer-Martin plates with sterile soybean casein digest broth. Standardize the suspension by adding additional sterile tryptic soy broth to yield 40% light transmission at 530nm wavelength.
components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
Soybean Casein Digest Broth: Composition per liter:
VCAT Inhibitor: Composition per 10.0mL:
Pancreatic digest of casein................................17.0g NaCl....................................................................5.0g Papaic digest of soybean meal............................3.0g K2HPO4...............................................................2.5g Glucose ...............................................................2.5g pH 7.3 ± 0.2 at 25°C
Source: The supplement solution IsoVitaleX enrichment is available from BD Diagnostic Systems. This enrichment may be replaced by supplement VX from BD Diagnostic Systems.
Colistin.............................................................7.5mg Trimethoprim lactate........................................5.0mg Vancomycin .....................................................4.0mg Anisomycin.......................................................0.02g
300
Maximum Recovery Diluent
Preparation of Soybean Casein Digest Broth:
Source: This medium is available as a premixed
Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
powder from Oxoid Unipath.
Supplement Solution: Composition per liter: Glucose ...........................................................100.0g L-Cysteine·HCl..................................................25.9g L-Glutamine.......................................................10.0g L-Cystine .............................................................1.1g Adenine...............................................................1.0g Nicotinamide adenine dinucleotide ..................0.25g Vitamin B12 .........................................................0.1g Thiamine pyrophosphate.....................................0.1g Guanine·HCl .....................................................0.03g Fe(NO3)3·6H2O .................................................0.02g p-Aminobenzoic acid......................................0.013g Thiamine·HCl ..................................................3.0mg
Preparation of Supplement Solution: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
PCAT Inhibitor: Composition per 10.0mL:
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: This diluent is a physiologically isotonic and protective medium for maximal recovery of microorganisms from a variety of sources.
McBride Listeria Agar Composition per liter: Agar ..................................................................15.0g Glycine..............................................................10.0g Pancreatic digest of casein..................................5.0g Peptic digest of animal tissue .............................5.0g NaCl....................................................................5.0g Beef extract.........................................................3.0g Phenylethyl alcohol ............................................2.5g LiCl .....................................................................0.5g pH 7.3 ± 0.22 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to
Anisomycin.......................................................0.02g Colistin.............................................................7.5mg Trimethoprim lactate........................................5.0mg Penicillin G ..................................................25,000U
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Preparation of PCAT Inhibitor: Add compo-
Use: For the selective isolation of Listeria monocy-
nents to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
togenes from clinical and nonclinical specimens containing mixed flora.
Preparation of Medium: Add components—except Sarcina lutea suspension, horse serum, supplement solution, and PCAT inhibitor—to distilled/ deionized water and bring volume to 940.0mL. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 20.0mL of sterile Sarcina lutea suspension, 20.0mL of sterile horse serum, 10.0mL of supplement solution, and 10.0mL of sterile PCAT inhibitor. Mix thoroughly. Pour into sterile Petri dishes.
Use: For the isolation and cultivation of pathogenic Neisseria, especially penicillinase-producing strains, from specimens containing mixed flora of bacteria and fungi.
Maximum Recovery Diluent Composition per liter: NaCl ....................................................................8.5g Peptone................................................................1.0g pH 7.0 ± 0.2 at 25°C
McCarthy Agar Composition per liter: Cornstarch.........................................................10.0g Naladixic acid .................................................0.015g Colistin..............................................................0.01g GC agar base...................................................... 1.0L pH 7.2 ± 0.2 at 25°C
GC Agar Base: Composition per liter: Agar ..................................................................10.0g Pancreatic digest of casein..................................7.5g Peptic digest of animal tissue .............................7.5g NaCl....................................................................5.0g K2HPO4...............................................................4.0g Cornstarch...........................................................1.0g KH2PO4...............................................................1.0g
Preparation of GC Agar Base: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly.
McClung-Toabe Agar, Modified Preparation of Medium: To 1.0L of GC agar base, add the cornstarch. Gently heat while stirring to dissolve. Add the naladixic acid and colistin. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes. Use: For the isolation and differentiation of Gardnerella vaginalis (Haemophilus vaginalis, Corynebacterium vaginale) from genitourinary specimens. Bacteria that can utilize starch appear as colonies surrounded by a clear zone.
McClung Carbon-Free Broth Composition per liter: NaNO3 ................................................................2.0g K2HPO4 ..............................................................0.8g MgSO4·7H2O ......................................................0.5g FeCl3 .................................................................0.01g MnCl2·4H2O ....................................................8.0mg ZnSO4 ..............................................................2.0mg pH 7.2 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat without boiling until salts dissolve. Cool to 25°C. Adjust pH to 7.2. Filter sterilize.
Use: For use as a basal medium in determining the carbon assimilation capabilities of microorganisms.
McClung-Toabe Agar Composition per liter: Proteose peptone ...............................................40.0g Agar ..................................................................25.0g Na2HPO4 .............................................................5.0g Glucose ...............................................................2.0g NaCl ....................................................................2.0g KH2PO4 ...............................................................1.0g MgSO4·7H2O ......................................................0.1g Egg yolk emulsion, 50%............................. 100.0mL pH 7.3 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Egg Yolk Emulsion, 50%: Composition per 100.0mL: Chicken egg yolks..................................................11 Whole chicken egg...................................................1 NaCl (0.9% solution) .................................... 50.0mL
Preparation of Egg Yolk Emulsion, 50%: Soak eggs with 1:100 dilution of saturated mercuric chloride solution for 1 min. Crack eggs and separate yolks from whites. Mix egg yolks with 1 chicken egg. Beat to form emulsion. Measure 50.0mL of egg yolk
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emulsion and add to 50.0mL of 0.9% NaCl solution. Mix thoroughly. Filter sterilize. Warm to 45°–50°C.
Preparation of Medium: Add components, except egg yolk emulsion, 50%, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Aseptically add 100.0mL of sterile egg yolk emulsion, 50%. Mix thoroughly. Pour into sterile Petri dishes in 15.0mL volumes.
Use: For the isolation and cultivation of Clostridium perfringens.
McClung-Toabe Agar, Modified Composition per liter: Proteose peptone no. 2......................................40.0g Agar ..................................................................20.0g Na2HPO4 .............................................................5.0g Glucose ...............................................................2.0g NaCl....................................................................2.0g KH2PO4...............................................................1.0g MgSO4·7H2O ......................................................0.1g Egg yolk emulsion, 50%............................. 100.0mL Hemin solution................................................ 1.0mL pH 7.6 ± 0.2 at 25°C
Egg Yolk Emulsion, 50%: Composition per 100.0mL: Chicken egg yolks.................................................. 11 Whole chicken egg ..................................................1 NaCl (0.9% solution) .................................... 50.0mL
Preparation of Egg Yolk Emulsion, 50%: Soak eggs with 1:100 dilution of saturated mercuric chloride solution for 1 min. Crack eggs and separate yolks from whites. Mix egg yolks with 1 chicken egg. Beat to form emulsion. Measure 50.0mL of egg yolk emulsion and add to 50.0mL of 0.9% NaCl solution. Mix thoroughly. Filter sterilize. Warm to 45°–50°C.
Hemin Solution: Composition per 100.0mL: Hemin .................................................................0.5g NaOH (1N solution)...................................... 20.0mL
Preparation of Hemin Solution: Add hemin to 20.0mL of 1N NaOH solution. Mix thoroughly. Bring volume to 100.0mL with distilled/deionized water.
Preparation of Medium: Add components, except egg yolk emulsion, 50%, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Aseptically add 100.0mL of sterile egg
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McClung-Toabe Agar, Modified
yolk emulsion, 50%. Mix thoroughly. Pour into sterile Petri dishes in 20.0mL volumes.
Use: For the cultivation of a wide variety of anaerobic bacteria. For the differentiation of anaerobic bacteria based on lecithinase production and lipase production. Bacteria that produce lecithinase appear as colonies surrounded by a zone of insoluble precipitate. Bacteria that produce lipase appear as colonies with a pearly iridescent sheen.
Use: For the cultivation of Clostridium species. For the differentiation of Clostridium species based on lecithinase production and lipase production. Bacteria that produce lecithinase appear as colonies surrounded by a zone of insoluble precipitate. Bacteria that produce lipase appear as colonies with a pearly iridescent sheen.
McClung-Toabe Agar, Modified Composition per liter:
McClung-Toabe Agar, Modified Composition per liter: Proteose peptone no. 2 ......................................40.0g Agar ..................................................................20.0g Na2HPO4 .............................................................5.0g Glucose ...............................................................2.0g NaCl ....................................................................2.0g KH2PO4 ...............................................................1.0g MgSO4·7H2O ......................................................0.1g Neomycin............................................................0.1g Egg yolk emulsion, 50%............................. 100.0mL Hemin solution................................................ 1.0mL pH 7.6 ± 0.2 at 25°C
Egg Yolk Emulsion, 50%: Composition per 100.0mL: Chicken egg yolks..................................................11 Whole chicken egg...................................................1 NaCl (0.9% solution) .................................... 50.0mL
Preparation of Egg Yolk Emulsion, 50%: Soak eggs with 1:100 dilution of saturated mercuric chloride solution for 1 min. Crack eggs and separate yolks from whites. Mix egg yolks with 1 chicken egg. Beat to form emulsion. Measure 50.0mL of egg yolk emulsion and add to 50.0mL of 0.9% NaCl solution. Mix thoroughly. Filter sterilize. Warm to 45°–50°C.
Hemin Solution: Composition per 100.0mL: Hemin..................................................................0.5g NaOH (1N solution)...................................... 20.0mL
Preparation of Hemin Solution: Add hemin to 20.0mL of 1N NaOH solution. Mix thoroughly. Bring volume to 100.0mL with distilled/deionized water.
Preparation of Medium: Add components, except egg yolk emulsion, 50%, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Aseptically add 100.0mL of sterile egg yolk emulsion, 50%. Mix thoroughly. Pour into sterile Petri dishes in 20.0mL volumes.
Proteose peptone no. 2......................................20.0g Agar ..................................................................20.0g Yeast extract........................................................5.0g Pancreatic digest of casein..................................5.0g NaCl....................................................................5.0g Sodium thioglycolate ..........................................1.0g Egg yolk emulsion, 50%............................... 80.0mL pH 7.6 ± 0.2 at 25°C
Egg Yolk Emulsion, 50%: Composition per 100.0mL: Chicken egg yolks.................................................. 11 Whole chicken egg ..................................................1 NaCl (0.9% solution) .................................... 50.0mL
Preparation of Egg Yolk Emulsion, 50%: Soak eggs with 1:100 dilution of saturated mercuric chloride solution for 1 min. Crack eggs and separate yolks from whites. Mix egg yolks with 1 chicken egg. Beat to form emulsion. Measure 50.0mL of egg yolk emulsion and add to 50.0mL of 0.9% NaCl solution. Mix thoroughly. Filter sterilize. Warm to 45°–50°C.
Preparation of Medium: Add components, except egg yolk emulsion, 50%, to distilled/deionized water and bring volume to 920.0mL. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Aseptically add 80.0mL of sterile egg yolk emulsion, 50%. Mix thoroughly. Pour into sterile Petri dishes in 20.0mL volumes.
Use: For the cultivation of Clostridium botulinum.
McClung-Toabe Egg Yolk Agar, CDC Modified (CDC Modified McClungToabe Egg Yolk Agar) Composition per liter: Pancreatic digest of casein................................40.0g Agar ..................................................................25.0g Na2HPO4 .............................................................5.0g Yeast extract........................................................5.0g Glucose ...............................................................2.0g NaCl....................................................................2.0g KH2PO4...............................................................1.0g
Membrane Lactose Glucuronide Agar
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Egg yolk emulsion, 50%............................. 100.0mL MgSO4·7H2O (5% solution) ........................... 0.2mL pH 7.3 ± 0.2 at 25°C
Preparation of Selective Supplement Solution: Add components to 4.0mL of distilled/deion-
Egg Yolk Emulsion, 50%: Composition per 100.0mL:
Phenolphthalein Biphosphate Tetrazolium Salt Solution: Composition per 10.0mL:
Chicken egg yolks..................................................11 Whole chicken egg...................................................1 NaCl (0.9% solution) .................................... 50.0mL
Preparation of Egg Yolk Emulsion, 50%: Soak eggs with 1:100 dilution of saturated mercuric chloride solution for 1 min. Crack eggs and separate yolks from whites. Mix egg yolks with 1 chicken egg. Beat to form emulsion. Measure 50.0mL of egg yolk emulsion and add to 50.0mL of 0.9% NaCl solution. Mix thoroughly. Filter sterilize. Warm to 45°–50°C.
Preparation of Medium: Add components—except egg yolk emulsion, 50%—to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Aseptically add 100.0mL of sterile egg yolk emulsion, 50%. Mix thoroughly. Pour into sterile Petri dishes in 15.0mL volumes.
Use: For the cultivation of a wide variety of anaerobic bacteria. For the differentiation of anaerobic bacteria based on lecithinase production, lipase production, and proteolytic ability. Bacteria that produce lecithinase appear as colonies surrounded by a zone of insoluble precipitate. Bacteria that produce lipase appear as colonies with a pearly iridescent sheen. Bacteria that produce proteolytic activity appear as colonies surrounded by a clear zone.
m-CP Medium Composition per liter: Tryptose ............................................................30.0g Yeast extract......................................................20.0g Agar ..................................................................15.0g Sucrose................................................................5.0g L-Cysteine·HCl·H2O ...........................................1.0g MgO4·7H2O ........................................................0.1g Bromcresol Purple ............................................0.04g Phenolphthalein biphosphate tetrazolium salt solution............................................. 10.0mL Selective supplement solution ........................ 4.0mL Indoxyl-β-D-glucoside solution ...................... 4.0mL Ferric chloride solution................................... 1.0mL pH 7.6 ± 0.2 at 25°C
Selective Supplement Solution: Composition per 4.0mL: D-Cycloserine......................................................0.4g
Polymyxin B sulfate.......................................25.0mg
ized water. Mix thoroughly. Filter sterilize.
Phenolphthalein biphosphate tetrazolium salt ...........................................................25.0mg
Preparation of Phenolphthalein Biphosphate Tetrazolium Salt Solution: Add phenolphthalein biphosphate tetrazolium salt to 10.0mL of distilled/ deionized water. Mix thoroughly. Filter sterilize.
Indoxyl-β-D-glucoside Solution: Composition per 10.0mL: Indoxyl-β-D-glucoside ......................................0.45g
Preparation of Indoxyl-β-D-glucoside Solution: Add indoxyl-β-D-glucoside to 10.0mL of distilled/deionized water. Mix thoroughly. Filter sterilize.
Feric Chloride Solution: Composition per 4.0mL: FeCl3·6H2O ....................................................30.0mg
Preparation of Feric Chloride Solution: Add FeCl3·6H2O to 4.0mL of distilled/deionized water. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components except selective supplement solution, phenolphthalein biphosphate tetrazolium salt solution, indoxyl-β-Dglucoside solution, and ferric chloride solution, to distilled/deionized water and bring volume to 981.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 4.0mL of selective supplement solution. Mix thoroughly. Aseptically add 10.0mL phenolphthalein biphosphate tetrazolium salt solution, 4.0mL indoxyl-β-D-glucoside solution, and 1.0mL ferric chloride solution. Mix thoroughly. Pour into sterile Petri dishes or aseptically distribute into tubes.
Use: A selective, chromogenic medium for the rapid identification and enumeration of Clostridium perfringens.
Membrane Lactose Glucuronide Agar (MLGA) Composition per liter: Peptone..................................................... 40.0g Lactose ..................................................... 30.0g Agar ......................................................... 10.0g Yeast extract............................................... 6.0g Sodium lauryl sulfate ................................. 1.0g Sodium pyruvate ........................................ 0.5g
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Methylene Blue Milk Medium
5-Bromo-4-chloro-3-indoxylβ-D-glucuronic acid ................................ 0.2g
Phenol Red................................................. 0.2g pH 7.4 ± 0.2 at 25°C
Source: This medium is available from Oxoid. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Pour into sterile Petri dishes.
Use: For the direct enumeration of E.coli and coliforms by the membrane filtration method. The chromogenic substrate 5-Bromo-4-chloro-3-indoxyl-β-D-glucuronic acid (BCIG), is cleaved by the enzyme β-glucuronidase and produces a blue chromophore that builds up within the bacterial cells. In addition, the incorporation of phenol red detects lactose fermentation and results in yellow colonies when acid is produced. Since coliform colonies are lactose positive, they will appear yellow on this medium and as E. coli colonies are both lactose and βglucuronidase positive, they will appear green.
Methylene Blue Milk Medium (MBM Medium) Composition per liter: Skim milk, dehydrated....................................100.0g Methylene Blue.................................................10.0g pH 6.4 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 20 min at 10 psi pressure–115°C.
Use: For the cultivation and differentiation of group D streptococci (enterococci) from other Streptococcus species.
MH IH Agar Composition per liter: Solution A ................................................... 490.0mL Solution B ................................................... 490.0mL Supplement solution ..................................... 20.0mL pH 6.9 ± 0.2 at 25°C
Solution A: Composition per 490.0mL: Beef infusion...................................................300.0g Acid hydrolysate of casein................................17.5g Agar ..................................................................17.0g Starch ..................................................................1.5g
Preparation of Solution A: Add components to distilled/deionized water and bring volume to
490.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C.
Solution B: Composition per 490.0mL: Hemoglobin ......................................................10.0g
Preparation of Solution B: Add hemoglobin to distilled/deionized water and bring volume to 490.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C.
Supplement Solution: Composition per liter: Glucose ...........................................................100.0g L-Cysteine·HCl..................................................25.9g L-Glutamine ......................................................10.0g L-Cystine .............................................................1.1g Adenine...............................................................1.0g Nicotinamide adenine dinucleotide ..................0.25g Vitamin B12 .........................................................0.1g Thiamine pyrophosphate ....................................0.1g Guanine·HCl .....................................................0.03g Fe(NO3)3·6H2O.................................................0.02g p-Aminobenzoic acid......................................0.013g Thiamine·HCl ..................................................3.0mg
Source: The supplement solution IsoVitaleX enrichment is available from BD Diagnostic Systems. This enrichment may be replaced by supplement VX from BD Diagnostic Systems.
Preparation of Supplement Solution: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
Preparation of Medium: Aseptically combine cooled, sterile solution A and cooled, sterile solution B. Mix thoroughly. Adjust pH to 6.9 with sterile 1N HCl or sterile 1N KOH. Aseptically add 20.0mL of sterile supplement solution. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation and differentiation of Legionella species.
Middlebrook 13A Medium Composition per 112.5mL: Casein hydrolysate..............................................0.1g Tween 80...........................................................0.02g Sodium polyanetholesulfonate........................0.025g Middlebrook 7H9 broth .............................. 100.0mL Middlebrook 13A enrichment....................... 12.5mL Catalase........................................................ 36,000U 14C-substrate ................................. 125µCi (185kBq) pH 6.6 ± 0.2 at 25°C
Middlebrook 7H9 Broth with Middlebrook OADC Enrichment Middlebrook 7H9 Broth: Composition per liter: Na2HPO4 .............................................................2.5g KH2PO4 ...............................................................1.0g Monosodium glutamate ......................................0.5g (NH4)2SO4...........................................................0.5g Sodium citrate .....................................................0.1g MgSO4·7H2O ....................................................0.05g Ferric ammonium citrate...................................0.04g CuSO4·5H2O ....................................................1.0mg Pyridoxine........................................................1.0mg ZnSO4·7H2O ....................................................1.0mg Biotin ...............................................................0.5mg CaCl2·2H2O......................................................0.5mg Glycerol .......................................................... 2.0mL
Preparation of Middlebrook 7H9 Broth: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly.
Middlebrook 13A Enrichment: Composition per 20.0mL: Bovine serum albumin ........................................3.0g
Preparation of Middlebrook 13A Enrichment: Add bovine serum albumin to distilled/deionized water and bring volume to 20.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: To 100.0mL of Middle-
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ment to other Middlebrook media for determining the antimicrobial susceptibility of mycobacteria.
Middlebrook 7H9 Broth with Middlebrook ADC Enrichment Composition per liter: Na2HPO4 .............................................................2.5g KH2PO4...............................................................1.0g Monosodium glutamate ......................................0.5g (NH4)2SO4 ..........................................................0.5g Sodium citrate.....................................................0.1g MgSO4·7H2O ....................................................0.05g Ferric ammonium citrate...................................0.04g CuSO4·5H2O ....................................................1.0mg Pyridoxine........................................................1.0mg ZnSO4·7H2O ....................................................1.0mg Biotin ...............................................................0.5mg CaCl2·2H2O .....................................................0.5mg Middlebrook ADC enrichment ................... 100.0mL Glycerol .......................................................... 2.0mL pH 6.6 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Middlebrook ADC Enrichment: Composition per 100.0mL: Bovine albumin fraction V .................................5.0g Glucose ...............................................................2.0g Catalase............................................................3.0mg
brook 7H9 broth, add remaining components, except Middlebrook 13A enrichment. Mix thoroughly. Filter sterilize. Aseptically distribute into bottles in 4.0mL volumes. Prior to inoculation, aseptically add 0.5mL of Middlebrook 13A enrichment to each bottle. Mix thoroughly.
Source: This enrichment is available as a prepared enrichment from BD Diagnostic Systems.
Use: For the cultivation of Mycobacterium species
and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
from the blood of patients suspected of having mycobacteremia.
Middlebrook ADC Enrichment (Middlebrook Albumin Dextrose Catalase Enrichment) Composition per 100.0mL: Bovine albumin fraction V .................................5.0g Glucose ...............................................................2.0g Catalase...........................................................0.003g
Source: This medium is available as a prepared enrichment from BD Diagnostic Systems.
Preparation of Enrichment: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation of Middlebrook ADC Enrichment: Add components to distilled/deionized water
Preparation of Medium: Add glycerol to 900.0mL of distilled/deionized water and add remaining components, except Middlebrook ADC enrichment. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 50°–55°C. Aseptically add 100.0mL of sterile Middlebrook ADC enrichment. Mix thoroughly. Distribute into sterile tubes or flasks.
Use: For the isolation, cultivation, and maintenance of Mycobacterium species, including Mycobacterium tuberculosis. Also used for determining the antimicrobial susceptibility of mycobacteria.
Middlebrook 7H9 Broth with Middlebrook OADC Enrichment
Use: For use as a supplement to other Middlebrook
Composition per liter:
media for the isolation, cultivation, and maintenance of Mycobacterium species. Also used as a supple-
Na2HPO4 .............................................................2.5g KH2PO4...............................................................1.0g
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Middlebrook 7H9 Broth with Middlebrook OADC Enrichment and Triton WR 1339
Monosodium glutamate ......................................0.5g (NH4)2SO4...........................................................0.5g Sodium citrate .....................................................0.1g MgSO4·7H2O ....................................................0.05g Ferric ammonium citrate...................................0.04g CuSO4·5H2O ....................................................1.0mg Pyridoxine........................................................1.0mg ZnSO4·7H2O ....................................................1.0mg Biotin ...............................................................0.5mg CaCl2·2H2O......................................................0.5mg Middlebrook OADC enrichment ................ 100.0mL Glycerol .......................................................... 2.0mL pH 6.6 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Middlebrook OADC Enrichment: Composition per 100.0mL: Bovine albumin fraction V .................................5.0g Glucose ...............................................................2.0g NaCl ..................................................................0.85g Oleic acid ..........................................................0.05g Catalase............................................................4.0mg
Source: This enrichment is available as a prepared enrichment from BD Diagnostic Systems.
Preparation of Middlebrook OADC Enrichment: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add glycerol to 900.0mL of distilled/deionized water and add remaining components, except Middlebrook OADC enrichment. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 50°–55°C. Aseptically add 100.0mL of sterile Middlebrook OADC enrichment. Mix thoroughly. Distribute into sterile tubes or flasks.
Use: For the isolation, cultivation, and maintenance of Mycobacterium species, including Mycobacterium tuberculosis. Also used for determining the antimicrobial susceptibility of mycobacteria.
Middlebrook 7H9 Broth with Middlebrook OADC Enrichment and Triton WR 1339 Composition per liter: Na2HPO4 .............................................................2.5g KH2PO4 ...............................................................1.0g Monosodium glutamate ......................................0.5g (NH4)2SO4...........................................................0.5g Sodium citrate .....................................................0.1g MgSO4·7H2O ....................................................0.05g Ferric ammonium citrate...................................0.04g
CuSO4·5H2O ....................................................1.0mg Pyridoxine........................................................1.0mg ZnSO4·7H2O ....................................................1.0mg Biotin ...............................................................0.5mg CaCl2·2H2O .....................................................0.5mg Middlebrook OADC enrichment with Triton WR 1339 ........................... 100.0mL Glycerol .......................................................... 2.0mL pH 6.6 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Middlebrook OADC Enrichment with Triton WR 1339: Composition per 100.0mL: Bovine albumin fraction V .................................5.0g Glucose ...............................................................2.0g NaCl..................................................................0.85g Triton WR 1339 ................................................0.25g Oleic acid ..........................................................0.05g Catalase............................................................4.0mg
Source: This enrichment is available as a prepared enrichment from BD Diagnostic Systems. Preparation of Middlebrook OADC Enrichment with Triton WR 1339: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add glycerol to 900.0mL of distilled/deionized water and add remaining components, except Middlebrook OADC enrichment with Triton WR-1339. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Aseptically add 100.0mL of sterile Middlebrook OADC enrichment with Triton WR-1339. Mix thoroughly. Distribute into sterile tubes or flasks.
Use: For the isolation, cultivation, and maintenance of Mycobacterium species, including Mycobacterium tuberculosis. Also used for determining the antimicrobial susceptibility of mycobacteria.
Middlebrook 7H9 Broth, Supplemented Composition per liter: Na2HPO4 .............................................................2.5g KH2PO4...............................................................1.0g Monosodium glutamate ......................................0.5g (NH4)2SO4 ..........................................................0.5g Tween 80.............................................................0.5g Sodium citrate.....................................................0.1g MgSO4·7H2O ....................................................0.05g Ferric ammonium citrate...................................0.04g Mycobactin J....................................................2.0mg CuSO4·5H2O ....................................................1.0mg
Middlebrook 7H10 Agar with Middlebrook OADC Enrichment Pyridoxine........................................................1.0mg ZnSO4·7H2O ....................................................1.0mg Biotin ...............................................................0.5mg CaCl2·2H2O......................................................0.5mg Dubos oleic albumin complex .................... 100.0mL Glycerol .......................................................... 2.0mL pH 6.6 ± 0.2 at 25°C
Source: Mycobactin J is available from Allied Laboratories, Inc.
Dubos Oleic Albumin Complex: Composition per 100.0mL: Bovine serum albumin, fraction V......................5.0g Oleic acid, sodium salt......................................0.05g NaCl (0.85% solution) ................................ 100.0mL
Preparation of Dubos Oleic Albumin Complex: Add bovine serum albumin and oleic acid to 100.0mL of NaCl solution. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except Dubos oleic albumin complex, to distilled/ deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile Dubos oleic albumin complex. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation and maintenance of Mycobacterium avium.
Middlebrook 7H10 Agar with Middlebrook ADC Enrichment Composition per liter: Agar ..................................................................15.0g Na2HPO4 .............................................................1.5g KH2PO4 ...............................................................1.5g (NH4)2SO4...........................................................0.5g L-Glutamic acid ...................................................0.5g Sodium citrate .....................................................0.4g Ferric ammonium citrate...................................0.04g MgSO4·7H2O ..................................................0.025g ZnSO4·7H2O ....................................................1.0mg CuSO4·5H2O ....................................................1.0mg Pyridoxine........................................................1.0mg Biotin ...............................................................0.5mg CaCl2·2H2O......................................................0.5mg Malachite Green.............................................0.25mg Middlebrook ADC enrichment ................... 100.0mL Glycerol .......................................................... 5.0mL pH 6.6 ± 0.2 at 25°C
Middlebrook ADC Enrichment: Composition per 100.0mL: Bovine albumin fraction V .................................5.0g Glucose ...............................................................2.0g Catalase...........................................................0.003g
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Source: The medium and enrichment are available as a prepared enrichment from BD Diagnostic Systems.
Preparation of Middlebrook ADC Enrichment: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add glycerol to 900.0mL of distilled/deionized water and add remaining components, except Middlebrook ADC enrichment. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 50°–55°C. Aseptically add 100.0mL of sterile Middlebrook ADC enrichment. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation, cultivation, and maintenance of Mycobacterium species, including Mycobacterium tuberculosis. Also used for determining the antimicrobial susceptibility of mycobacteria.
Middlebrook 7H10 Agar with Middlebrook OADC Enrichment (Middlebrook and Cohn 7H10 Agar) Composition per liter: Agar ..................................................................15.0g Na2HPO4 .............................................................1.5g KH2PO4...............................................................1.5g (NH4)2SO4 ..........................................................0.5g L-Glutamic acid...................................................0.5g Sodium citrate.....................................................0.4g Ferric ammonium citrate...................................0.04g MgSO4·7H2O ..................................................0.025g ZnSO4·7H2O ....................................................1.0mg CuSO4·5H2O ....................................................1.0mg Pyridoxine........................................................1.0mg Biotin ...............................................................0.5mg CaCl2·2H2O .....................................................0.5mg Malachite Green.............................................0.25mg Middlebrook OADC enrichment ................ 100.0mL Glycerol .......................................................... 5.0mL pH 6.6 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Middlebrook OADC Enrichment: Composition per 100.0mL: Bovine albumin fraction V .................................5.0g Glucose ...............................................................2.0g NaCl..................................................................0.85g Oleic acid ..........................................................0.05g Catalase............................................................4.0mg
308
Middlebrook 7H10 Agar with Middlebrook OADC Enrichment and Hemin
Source: This enrichment is available as a prepared enrichment from BD Diagnostic Systems.
Preparation of Middlebrook OADC Enrichment: Add components to distilled/deionized water
Preparation of Middlebrook OADC Enrichment: Add components to distilled/deionized water
and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Hemin Solution: Composition per 100.0mL:
Preparation of Medium: Add glycerol to
Hemin .................................................................1.0g NaOH (1N solution)...................................... 20.0mL
900.0mL of distilled/deionized water and add remaining components, except Middlebrook OADC enrichment. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 50°–55°C. Aseptically add 100.0mL of sterile Middlebrook OADC enrichment. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation, cultivation, and maintenance of Mycobacterium species, including Mycobacterium tuberculosis. Also used for determining the antimicrobial susceptibility of mycobacteria.
Middlebrook 7H10 Agar with Middlebrook OADC Enrichment and Hemin (Hemin Medium for Mycobacterium) Composition per liter: Agar ..................................................................15.0g Na2HPO4 .............................................................1.5g KH2PO4 ...............................................................1.5g (NH4)2SO4...........................................................0.5g L-Glutamic acid ...................................................0.5g Sodium citrate .....................................................0.4g Ferric ammonium citrate...................................0.04g MgSO4·7H2O ..................................................0.025g ZnSO4·7H2O ....................................................1.0mg CuSO4·5H2O ....................................................1.0mg Pyridoxine........................................................1.0mg Biotin ...............................................................0.5mg CaCl2·2H2O......................................................0.5mg Malachite Green.............................................0.25mg Middlebrook OADC enrichment ................ 100.0mL Glycerol .......................................................... 5.0mL Hemin solution................................................ 3.9mL pH 6.6 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Middlebrook OADC Enrichment: Composition per 100.0mL: Bovine albumin fraction V .................................5.0g Glucose ...............................................................2.0g NaCl ..................................................................0.85g Oleic acid ..........................................................0.05g Catalase............................................................4.0mg
Preparation of Hemin Solution: Add hemin to 20.0mL of 1N NaOH solution. Mix thoroughly. Bring volume to 100.0mL with distilled/deionized water.
Preparation of Medium: Add glycerol to 891.1mL of distilled/deionized water and add remaining components, except Middlebrook OADC enrichment. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 50°–55°C. Aseptically add 100.0mL of sterile Middlebrook OADC enrichment. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation, cultivation, and maintenance of Mycobacterium species, including Mycobacterium tuberculosis. For the cultivation and maintenance of Mycobacterium haemophilum. Also used for determining the antimicrobial susceptibility of mycobacteria.
Middlebrook 7H10 Agar with Middlebrook OADC Enrichment and Triton WR 1339 Composition per liter: Agar ..................................................................15.0g Na2HPO4 .............................................................1.5g KH2PO4...............................................................1.5g (NH4)2SO4 ..........................................................0.5g L-Glutamic acid...................................................0.5g Sodium citrate.....................................................0.4g Ferric ammonium citrate...................................0.04g MgSO4·7H2O ..................................................0.025g ZnSO4·7H2O ....................................................1.0mg CuSO4·5H2O ....................................................1.0mg Pyridoxine........................................................1.0mg Biotin ...............................................................0.5mg CaCl2·2H2O .....................................................0.5mg Malachite Green.............................................0.25mg Middlebrook OADC enrichment with Triton WR 1339 ........................... 100.0mL Glycerol .......................................................... 5.0mL pH 6.6 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Middlebrook 7H11 Agar, Selective Middlebrook OADC Enrichment with Triton WR 1339: Composition per 100.0mL: Bovine albumin fraction V .................................5.0g Glucose ...............................................................2.0g NaCl ..................................................................0.85g Triton WR 1339 ................................................0.25g Oleic acid ..........................................................0.05g Catalase............................................................4.0mg
Source: This enrichment is available as a prepared enrichment from BD Diagnostic Systems.
Preparation of Middlebrook OADC Enrichment with Triton WR 1339: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add glycerol to 900.0mL of distilled/deionized water and add remaining components, except Middlebrook OADC enrichment with Triton WR-1339. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Aseptically add 100.0mL of sterile Middlebrook OADC enrichment with Triton WR-1339. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation, cultivation, and maintenance of Mycobacterium species, including Mycobacterium tuberculosis. Also used for determining the antimicrobial susceptibility of mycobacteria.
Middlebrook 7H10 Agar with Streptomycin Composition per liter: Agar ..................................................................15.0g Na2HPO4 .............................................................1.5g KH2PO4 ...............................................................1.5g (NH4)2SO4...........................................................0.5g L-Glutamic acid ...................................................0.5g Sodium citrate .....................................................0.4g Ferric ammonium citrate...................................0.04g MgSO4·7H2O ..................................................0.025g ZnSO4·7H2O ....................................................1.0mg CuSO4·5H2O ....................................................1.0mg Pyridoxine........................................................1.0mg Biotin ...............................................................0.5mg CaCl2·2H2O......................................................0.5mg Malachite Green.............................................0.25mg Glycerol .......................................................... 5.0mL Streptomycin ................................................100.0mg pH 6.6 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
309
Preparation of Medium: Add glycerol to 1.0L of distilled/deionized water and add remaining components. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Aseptically add streptomycin. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes. Use: For the isolation, cultivation, and maintenance of Mycobacterium kansasii.
Middlebrook 7H11 Agar, Selective Composition per liter: Agar ..................................................................15.0g Na2HPO4 .............................................................1.5g KH2PO4...............................................................1.5g Pancreatic digest of casein..................................1.0g (NH4)2SO4 ..........................................................0.5g L–Glutamic acid ..................................................0.5g Sodium citrate.....................................................0.4g MgSO4·7H2O ....................................................0.05g Ferric ammonium citrate...................................0.04g Pyridoxine........................................................1.0mg ZnSO4·7H2O ....................................................1.0mg CuSO4·5H2O ....................................................1.0mg CaCl2·2H2O .....................................................0.5mg Malachite Green.............................................0.25mg D–Biotin ............................................................0.5µg Middlebrook OADC enrichment ................ 100.0mL Antibiotic solution ........................................ 10.0mL Glycerol .......................................................... 5.0mL pH 6.6 ± 0.2 at 25°C
Middlebrook OADC Enrichment: Composition per 100.0mL: Bovine albumin fraction V .................................5.0g Glucose ...............................................................2.0g NaCl..................................................................0.85g Oleic acid ..........................................................0.05g Catalase............................................................4.0mg
Source: This enrichment is available as a prepared enrichment from BD Diagnostic Systems. Preparation of Middlebrook OADC Enrichment: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Antibiotic Solution: Composition per 10.0mL: Carbenicillin ..................................................0.05mg Trimethoprim lactate......................................0.02mg Amphotericin B .............................................0.01mg Polymyxin B .............................................. 200,000U
310
Middlebrook 7H11 Agar with Middlebrook ADC Enrichment
Preparation of Antibiotic Solution: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add glycerol to 890.0mL of distilled/deionized water and add remaining components, except Middlebrook OADC enrichment and antibiotic solution. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Aseptically add 100.0mL of sterile Middlebrook OADC enrichment and 10.0mL of sterile antibiotic solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the selective isolation and cultivation of pathogenic mycobacteria from specimens potentially contaminated with bacteria and fungi.
Middlebrook 7H11 Agar with Middlebrook ADC Enrichment (Mycobacteria 7H11 Agar with Middlebrook ADC Enrichment) Composition per liter: Agar ..................................................................15.0g Na2HPO4 .............................................................1.5g KH2PO4 ...............................................................1.5g Pancreatic digest of casein..................................1.0g (NH4)2SO4...........................................................0.5g L-Glutamic acid...................................................0.5g Sodium citrate .....................................................0.4g MgSO4·7H2O ....................................................0.05g Ferric ammonium citrate...................................0.04g Pyridoxine........................................................1.0mg Malachite Green.............................................0.25mg D-Biotin............................................................ 0.5µg Middlebrook ADC enrichment ................... 100.0mL Glycerol .......................................................... 5.0mL pH 6.6 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Middlebrook ADC Enrichment: Composition per 100.0mL: Bovine albumin fraction V .................................5.0g Glucose ...............................................................2.0g Catalase...........................................................0.003g
maining components, except Middlebrook ADC enrichment. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 50°–55°C. Aseptically add 100.0mL of sterile Middlebrook ADC enrichment. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation of drug-resistant (isoniazid [INH]) strains of Mycobacterium tuberculosis. For the cultivation of particularly fastidious strains of tubercle bacilli that occur following treatment of tuberculosis patients with secondary antitubercular drugs. Generally, these strains fail to grow on 7H10 medium.
Middlebrook 7H11 Agar with Middlebrook OADC Enrichment (Mycobacteria 7H11 Agar with Middlebrook OADC Enrichment) Composition per liter: Agar ..................................................................15.0g Na2HPO4 .............................................................1.5g KH2PO4...............................................................1.5g Pancreatic digest of casein..................................1.0g (NH4)2SO4 ..........................................................0.5g L-Glutamic acid ..................................................0.5g Sodium citrate.....................................................0.4g MgSO4·7H2O ....................................................0.05g Ferric ammonium citrate...................................0.04g Pyridoxine........................................................1.0mg Malachite Green.............................................0.25mg D-Biotin.............................................................0.5µg Middlebrook OADC enrichment ................ 100.0mL Glycerol .......................................................... 5.0mL pH 6.6 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Middlebrook OADC Enrichment: Composition per 100.0mL: Bovine albumin fraction V .................................5.0g Glucose ...............................................................2.0g NaCl..................................................................0.85g Oleic acid ..........................................................0.05g Catalase............................................................4.0mg
enrichment from BD Diagnostic Systems.
Source: This enrichment is available as a prepared enrichment from BD Diagnostic Systems.
Preparation of Middlebrook ADC Enrichment: Add components to distilled/deionized water
Preparation of Middlebrook OADC Enrichment: Add components to distilled/deionized water
and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add glycerol to
Preparation of Medium: Add glycerol to
900.0mL of distilled/deionized water and add re-
900.0mL of distilled/deionized water and add re-
Source: This enrichment is available as a prepared
Middlebrook 7H12 Medium maining components, except Middlebrook OADC enrichment. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 50°–55°C. Aseptically add 100.0mL of sterile Middlebrook OADC enrichment. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation of drug-resistant (isoniazid [INH]) strains of Mycobacterium tuberculosis. For the cultivation of particularly fastidious strains of tubercle bacilli that occur following treatment of tuberculosis patients with secondary antitubercular drugs. Generally, these strains fail to grow on 7H10 medium.
311
Preparation of Middlebrook OADC Enrichment with Triton WR 1339: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add glycerol to 900.0mL of distilled/deionized water and add remaining components, except Middlebrook OADC enrichment with Triton WR-1339. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Aseptically add 100.0mL of sterile Middlebrook OADC enrichment with Triton WR-1339. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation of drug-resistant (isoniazid
Middlebrook 7H11 Agar with Middlebrook OADC Enrichment and Triton WR 1339 (Mycobacteria 7H11 Agar with Middlebrook OADC Enrichment and Triton WR 1339) Composition per liter: Agar ..................................................................15.0g Na2HPO4 .............................................................1.5g KH2PO4 ...............................................................1.5g Pancreatic digest of casein..................................1.0g (NH4)2SO4...........................................................0.5g L-Glutamic acid...................................................0.5g Sodium citrate .....................................................0.4g MgSO4·7H2O ....................................................0.05g Ferric ammonium citrate...................................0.04g Pyridoxine........................................................1.0mg Malachite Green.............................................0.25mg D-Biotin............................................................ 0.5µg Middlebrook OADC enrichment with Triton WR 1339............................ 100.0mL Glycerol .......................................................... 5.0mL pH 6.6 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Middlebrook OADC Enrichment with Triton WR 1339: Composition per 100.0mL: Bovine albumin fraction V .................................5.0g Glucose ...............................................................2.0g NaCl ..................................................................0.85g Triton WR 1339 ................................................0.25g Oleic acid ..........................................................0.05g Catalase............................................................4.0mg
Source: This enrichment is available as a prepared enrichment from BD Diagnostic Systems.
[INH]) strains of Mycobacterium tuberculosis. For the cultivation of particularly fastidious strains of tubercle bacilli that occur following treatment of tuberculosis patients with secondary antitubercular drugs. Generally, these strains fail to grow on 7H10 medium.
Middlebrook 7H12 Medium Composition per 102.5mL: Bovine serum albumin........................................0.5g Casein hydrolyslate.............................................0.1g Catalase........................................................... 4800U 14C-Palmitic acid ...........................................100µCi Middlebrook 7H9 broth .............................. 100.0mL Antibiotic solution .......................................... 2.5mL pH 6.8 ± 0.1 at 25°C
Middlebrook 7H9 Broth: Composition per liter: Na2HPO4 .............................................................2.5g KH2PO4...............................................................1.0g Monosodium glutamate ......................................0.5g (NH4)2SO4 ..........................................................0.5g Sodium citrate.....................................................0.1g MgSO4·7H2O ....................................................0.05g Ferric ammonium citrate...................................0.04g CuSO4·5H2O ....................................................1.0mg Pyridoxine........................................................1.0mg ZnSO4·7H2O ....................................................1.0mg Biotin ...............................................................0.5mg CaCl2·2H2O .....................................................0.5mg Glycerol .......................................................... 2.0mL
Preparation of Middlebrook 7H9 Broth: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly.
Antibiotic Solution: Composition per 5.0mL: Nalidixic acid......................................................0.2g Azlocillin ............................................................0.1g Amphotericin B ................................................0.05g
312
Middlebrook Medium
Trimethoprim ....................................................0.05g Polymyxin B ..............................................500,000U
Preparation of Antibiotic Solution: Add components to distilled/deionized water and bring volume to 5.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: To 100.0mL of Middlebrook 7H9 broth, add remaining components, except antibiotic solution. Mix thoroughly. Filter sterilize. Aseptically distribute into bottles in 4.0mL volumes. Prior to inoculation, aseptically add 0.1mL of antibiotic solution to each bottle. Mix thoroughly.
enrichment. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 50°–55°C. Aseptically add 100.0mL of sterile Middlebrook OADC enrichment. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation, cultivation, and maintenance of Mycobacterium species.
Middlebrook Medium with Mycobactin (DSMZ Medium 780)
Use: For the cultivation of Mycobacterium species
Composition per liter:
from the blood of patients suspected of having mycobacteremia.
Agar ..................................................................15.0g Na2HPO4 .............................................................1.5g KH2PO4...............................................................1.5g (NH4)2SO4 ..........................................................0.5g L-Glutamic acid...................................................0.5g Sodium citrate.....................................................0.4g Ferric ammonium citrate...................................0.04g MgSO4·7H2O ..................................................0.025g Mycobactin J....................................................2.0mg ZnSO4·7H2O ....................................................1.0mg CuSO4·5H2O ....................................................1.0mg Pyridoxine........................................................1.0mg Biotin ...............................................................0.5mg CaCl2·2H2O .....................................................0.5mg Malachite Green.............................................0.25mg Middlebrook ADC enrichment ................... 100.0mL Glycerol .......................................................... 5.0mL pH 6.6 ± 0.2 at 25°C
Middlebrook Medium (DSMZ Medium 645) Composition per liter: Agar ..................................................................15.0g Na2HPO4 .............................................................1.5g KH2PO4 ...............................................................1.5g (NH4)2SO4...........................................................0.5g L-Glutamic acid ...................................................0.5g Sodium citrate .....................................................0.4g Ferric ammonium citrate...................................0.04g MgSO4·7H2O ..................................................0.025g ZnSO4·7H2O ....................................................1.0mg CuSO4·5H2O ....................................................1.0mg Pyridoxine........................................................1.0mg Biotin ...............................................................0.5mg CaCl2·2H2O......................................................0.5mg Malachite Green.............................................0.25mg Middlebrook OADC enrichment ................ 100.0mL Glycerol .......................................................... 5.0mL pH 6.6 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Middlebrook OADC Enrichment: Composition per 100.0mL: Bovine albumin fraction V .................................5.0g Glucose ...............................................................2.0g Catalase...........................................................0.003g Distilled water............................................. 100.0mL
Source: This enrichment is available as a prepared enrichment from BD Diagnostic Systems.
Preparation of Middlebrook OADC Enrichment: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add glycerol to 900.0mL of distilled/deionized water and add remaining components, except Middlebrook OADC
Source: Mycobactin J is available from Allied Laboratories, Inc.
Middlebrook ADC Enrichment: Composition per 100.0mL: Bovine albumin fraction V .................................5.0g Glucose ...............................................................2.0g Catalase...........................................................0.003g Distilled water............................................. 100.0mL
Source: This medium and enrichment is available from BD Diagnostic Systems. Preparation of Middlebrook ADC Enrichment: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add glycerol to 900.0mL of distilled/deionized water and add remaining components, except Middlebrook ADC enrichment and mycobactin. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Aseptically add 100.0mL of sterile Middlebrook ADC enrichment and mycobactin. The mycobactin is dissolved
Minimum Essential Medium with Bicarbonate, Serum, and Antibiotics in 2.0mL ethanol. Be sure to add all of the mycobactin; wash with additional 2.0mL ethanol if needed. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation of Mycobacterium avium subsp. paratuberculosis.
Middlebrook OADC Enrichment (Middlebrook Oleic Albumin Dextrose Catalase Enrichment) Composition per 100.0mL: Bovine albumin fraction V .................................5.0g Glucose ...............................................................2.0g NaCl ..................................................................0.85g Oleic acid ..........................................................0.05g Catalase............................................................4.0mg
Source: This medium is available as a prepared enrichment from BD Diagnostic Systems.
Preparation of Enrichment: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize. Use: For use as a supplement to other Middlebrook media for the isolation, cultivation, and maintenance of Mycobacterium species. Also used as a supplement to other Middlebrook media for determining the antimicrobial susceptibility of mycobacteria.
313
MIL Medium (Motility Indole Lysine Medium) Composition per liter: Peptone .............................................................10.0g Pancreatic digest of casein................................10.0g L-Lysine·HCl .....................................................10.0g Yeast extract........................................................3.0g Agar ....................................................................2.0g Dextrose..............................................................1.0g Ferric ammonium citrate.....................................0.5g Bromcresol Purple ............................................0.02g pH 6.6 ± 0.2 at 25°C
Source: This medium is available as a premixed powder and prepared medium from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes in 5.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation and differentiation of members of the Enterobacteriaceae on the basis of motility, lysine decarboxylase activity, lysine deaminase activity, and indole production.
Minimum Essential Medium with Bicarbonate, Serum, and Antibiotics Composition per 1100.0mL:
Middlebrook OADC Enrichment with Triton WR 1339 (Middlebrook Oleic Albumin Dextrose Catalase Enrichment with Triton WR 1339) Composition per 100.0mL: Bovine albumin fraction V .................................5.0g Glucose ...............................................................2.0g NaCl ..................................................................0.85g Triton WR 1339 ................................................0.25g Oleic acid ..........................................................0.05g Catalase............................................................4.0mg
Source: This medium is available as a prepared enrichment from BD Diagnostic Systems.
Minimum essential medium ....................... 950.0mL Fetal bovine serum, heat inactivated .......... 100.0mL NaHCO3 solution .......................................... 40.0mL Penicillin-streptomycin solution................... 10.0mL pH 7.2 ± 0.2 at 25°C
Minimum Essential Medium (MEM): Composition per liter: Inorganic salt solution................................. 400.0mL Other component solution........................... 400.0mL Amino acid solution.................................... 100.0mL Vitamin solution.......................................... 100.0mL
Inorganic Salt Solution: Composition per 400.0mL:
Use: For use as a supplement to other Middlebrook
NaCl....................................................................6.8g KCl......................................................................0.4g CaCl2, anhydrous ................................................0.2g NaH2PO4·H2O...................................................0.14g MgSO4, anhydrous.......................................97.67mg
media for the isolation, cultivation, and maintenance of Mycobacterium species. Also used as a supplement to other Middlebrook media for determining the antimicrobial susceptibility of mycobacteria.
components to distilled/deionized water and bring volume to 400.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C.
Preparation of Enrichment: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation of Inorganic Salt Solution: Add
314
Mitis-Salivarius Agar
Other Component Solution: Composition per 400.0mL:
NaHCO3 Solution: Composition per 40.0mL:
D-Glucose............................................................1.0g
NaHCO3 ..............................................................2.0g
Phenol Red.....................................................10.0mg
Preparation of NaHCO3 Solution: Add
Preparation of Other Component Solution: Add components to distilled/deionized water and bring volume to 400.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C.
Amino Acid Solution: Composition per 100.0mL: L-Glutamine .................................................292.0mg L-Arginine·HCl ............................................126.1mg L-Lysine·HCl..................................................72.5mg L-Isoleucine....................................................52.0mg L-Leucine .......................................................52.0mg L-Tyrosine,
disodium salt...............................52.0mg L-Threonine....................................................48.0mg L-Valine ..........................................................46.0mg L-Histidine·HCl·H2O......................................42.0mg L-Phenylalanine .............................................32.0mg L-Cysteine·2HCl ............................................31.0mg L-Methionine..................................................15.0mg L-Glutamic acid..............................................14.7mg L-Aspartic acid ...............................................13.3mg L-Asparagine·H2O..........................................13.2mg L-Proline.........................................................11.5mg L-Serine ..........................................................10.5mg L-Tryptophan..................................................10.0mg L-Alanine .........................................................8.9mg Glycine.............................................................7.5mg
Preparation of Amino Acid Solution: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Vitamin Solution: Composition per 100.0mL: i-Inositol...........................................................2.0mg D-Ca pantothenate ............................................1.0mg Choline chloride...............................................1.0mg Folic acid..........................................................1.0mg Niacinamide .....................................................1.0mg Pyridoxal·HCl ..................................................1.0mg Thiamine·HCl ..................................................1.0mg Riboflavin ........................................................0.1mg
Preparation of Vitamin Solution: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation of Minimum Essential Medium (MEM): Aseptically combine 400.0mL of sterile inorganic salt solution, 400.0mL of sterile other component solution, 100.0mL of sterile amino acid solution, and 100.0mL of sterile vitamin solution.
NaHCO3 to distilled/deionized water and bring volume to 40.0mL. Mix thoroughly. Filter sterilize.
Penicillin-Streptomycin Solution: Composition per 10.0mL: Penicillin ...........................................................0.01g Streptomycin.....................................................0.01g
Preparation of Penicillin-Streptomycin Solution: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Aseptically combine 950.0mL of sterile minimum essential medium, 100.0mL of sterile heat inactivated fetal bovine serum, 40.0mL of sterile NaHCO3 solution, and 10.0mL of sterile penicillin-streptomycin solution. Adjust pH to 7.2 with humidified 10% CO2 in 90% air.
Use: For the cultivation of Encephalitozoon cuniculi, Encephalitozoon hellem, Encephalitozoon intestinalis, Naegleria fowleri, and Nosema corneum.
Mitis-Salivarius Agar Composition per liter: Sucrose..............................................................50.0g Agar ..................................................................15.0g Enzymatic digest of protein ..............................10.0g Proteose peptone...............................................10.0g K2HPO4...............................................................4.0g Dextrose..............................................................1.0g Trypan Blue ......................................................0.08g Crystal Violet ...................................................0.8mg Na2TeO3 solution ............................................ 1.0mL pH 7.0 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Na2TeO3 Solution: Composition per 10.0mL: Na2TeO3 ..............................................................0.1g
Preparation of Na2TeO3 Solution: Add
Na2TeO3 to 10.0mL of distilled/deionized water. Mix thoroughly. Filter sterilize.
Caution: Potassium tellurite is toxic. Preparation of Medium: Add components to distilled/deionized water and bring volume to 999.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool medium to 50°–55°C. Aseptically add
Motility GI Medium 1.0mL of the sterile Na2TeO3 solution to the cooled basal medium. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the selective isolation of Streptococcus mitis, Streptococcus salivarius, and other viridans streptococci and enterococci.
Møller Decarboxylase Broth Composition per liter: Amino acid........................................................10.0g Peptic digest of animal tissue..............................5.0g Beef extract .........................................................5.0g Glucose ...............................................................0.5g Bromcresol Purple ............................................0.01g Cresol Red........................................................5.0mg Pyridoxal..........................................................5.0mg pH 6.0 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Use L-lysine, L-arginine, or L-ornithine. Mix thoroughly. Gently heat until dissolved. Distribute into screw-capped tubes in 5.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C. A slight precipitate may form in the ornithine broth.
Use: For the differentiation of Gram-negative enteric bacteria based on the production of arginine dihydrolase, lysine decarboxylase, or ornithine decarboxylase.
Molybdate Agar Composition per101.5mL: Base............................................................. 100.0mL Phosphomolybdic acid solution ...................... 1.5mL pH 5.3 ± 0.2 at 25°C
Base: Composition per liter: Sucrose..............................................................40.0g Agar ..................................................................15.0g Meat peptone.....................................................10.0g
Preparation of Base: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.6. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C.
Phosphomolybdic Acid Solution: Composition per 100.0mL: P2O5·2OMoO3 ...................................................12.5g
Preparation of Phosphomolybdic Acid Solution: Add P2O5·2OMoO3 (phospho-12-molybdic ac-
id, 12–molybdophosphoric acid, or PMA) to sterile
315
distilled/deionized water. Mix thoroughly. Do not adjust pH.
Preparation of Medium: To 100.0mL of cooled sterile base, add 1.5mL of phosphomolybdic acid solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes. Use: For the isolation and presumptive identification of yeast, especially Candida species. Candida albicans appears as smooth, medium olive colonies with medium olive bottoms. Candida stellatoidea appears as shiny, light gray colonies with light gray bottoms. Candida tropicalis appears as smooth, shiny, dark blue/gray colonies with dark blue/gray bottoms. Candida krusei appears as smooth, dull white colonies with white bottoms. Saccharomyces cerevisiae appears as smooth, shiny light blue/dark blue colonies with dark blue/green bottoms.
Monsur Agar (Taurocholate Tellurite Gelatin Agar) Composition per liter: Gelatin...............................................................30.0g Agar ..................................................................15.0g Casein peptone..................................................10.0g NaCl..................................................................10.0g Sodium taurocholate ...........................................5.0g Na2CO3 ·H2O ......................................................1.0g K2TeO3 solution............................................ 10.0mL pH 8.5 ± 0.2 at 25°C
K2TeO3 Solution: Composition per 10.0mL: K2TeO3 ..............................................................0.02g
Preparation of K2TeO3 Solution: Add K2TeO3 to 10.0mL of distilled/deionized water. Mix thoroughly. Filter sterilize.
Caution: Potassium tellurite is toxic. Preparation of Medium: Add components, except K2TeO3 solution, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Add 10.0mL of sterile K2TeO3 solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation of Vibrio cholerae from fecal specimens.
Motility GI Medium Composition per liter: Gelatin...............................................................53.4g Heart infusion broth..........................................25.0g Agar ....................................................................3.0g pH 7.2 ± 0.2 at 25°C
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Motility Indole Ornithine Medium
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
um chloride to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components to
Preparation of Medium: Add components, ex-
cold distilled/deionized water and bring to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes in 20.0mL volumes or leave in tubes.
Use: For demonstrating the motility of microorganisms and for separating organisms in their motile phase.
cept 2,3,5-triphenyltetrazolium chloride solution, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 60°C. Aseptically add 10.0mL of the sterile 2,3,5-triphenyltetrazolium chloride solution. Mix thoroughly. Aseptically distribute into sterile tubes. Keep at 4°–8°C until used.
Use: For the determination of bacterial motility.
Motility Indole Ornithine Medium (MIO Medium) Composition per liter: Pancreatic digest of gelatin ...............................10.0g Pancreatic digest of casein..................................9.5g L-Ornithine·HCl ..................................................5.0g Yeast extract........................................................3.0g Agar ....................................................................2.0g Glucose ...............................................................1.5g Bromcresol Purple ............................................0.02g pH 6.6 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components to distilled/deionized water and bring to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the differentiation of Gram-negative enteric bacteria based on their motility, indole production, and ornithine decarboxylase activity.
Motility Medium S Composition per liter: Beef heart, solids from infusion......................500.0g Gelatin...............................................................30.0g Enzymatic hydrolyzate of protein.....................10.0g NaCl ....................................................................5.0g K2HPO4 ...............................................................2.0g KNO3 ..................................................................2.0g Agar ....................................................................1.0g 2,3,5-Triphenyltetrazolium chloride solution ..................................... 10.0mL pH 7.2 ± 0.2 at 25°C
2,3,5-Triphenyltetrazolium Chloride Solution: Composition per 10.0mL: 2,3,5-Triphenyltetrazolium chloride ...................0.1g
Preparation of 2,3,5-Triphenyltetrazolium Chloride Solution: Add 2,3,5-triphenyltetrazoli-
Motility Nitrate Agar Composition per liter: Beef heart, solids from infusion......................100.0g Tryptose ............................................................12.0g Agar ....................................................................3.0g NaCl....................................................................1.0g KNO3 ..................................................................1.0g Glucose ...............................................................0.5g pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes in 4.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation and observation of motility and nitrate reduction in a variety of Gram-negative bacteria.
Motility Nitrate Medium (FDA M101) Composition per liter: Beef heart, solids from infusion......................100.0g Tryptose ............................................................12.0g Agar ....................................................................3.0g NaCl....................................................................1.0g KNO3, nitrite free ...............................................1.0g pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into screw-capped tubes in 4.0mL volumes. Autoclave for 15 min at 15 psi pressure– 121°C.
Use: For the cultivation and differentiation of Gramnegative nonfermentative bacteria from cosmetics based on their motility and their ability to reduce nitrate to nitrite.
Motility Test and Maintenance Medium
Motility Nitrate Medium Composition per liter: Beef heart, solids from infusion......................100.0g Tryptose ............................................................12.0g Agar ....................................................................3.0g NaCl ....................................................................1.0g KNO3 ..................................................................1.0g
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes in 4.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation and observation of motility and nitrate reduction in a variety of Gram-negative nonfermentative bacteria isolated from cosmetics.
Motility Nitrate Medium, Buffered Composition per liter: Peptone................................................................5.0g Galactose.............................................................5.0g Agar ....................................................................3.0g Beef extract .........................................................3.0g Na2HPO4 .............................................................2.5g KNO3 ..................................................................1.0g Glycerin .......................................................... 5.0mL pH 7.3 ± 0.1 at 25°C
Preparation of Medium: Add components, except agar, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat until dissolved. Add agar. Gently heat until boiling. Distribute into tubes in 11.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C. If not used within 4 hr, heat tubes to 100°C for 10 min.
Use: For the cultivation and observation of the motility of Clostridium perfringens.
Motility Sulfide Medium Composition per liter: Gelatin...............................................................80.0g Proteose peptone ...............................................10.0g NaCl ....................................................................5.0g Agar ....................................................................4.0g Beef extract .........................................................3.0g Sodium citrate .....................................................2.0g L-Cystine .............................................................0.2g Ferrous ammonium citrate ..................................0.2g pH 7.3 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring
317
to boiling. Distribute into tubes in 4–5.0mL volumes. Autoclave for 15 min at 10 psi pressure–116°C.
Use: For the determination of bacterial motility and the ability of bacteria to produce H2S from L-cystine. For the differentiation of Gram-negative bacteria of the Enterobacteriaceae.
Motility Test and Maintenance Medium Composition per liter: Peptone .............................................................10.0g NaCl....................................................................5.0g Agar ....................................................................4.0g Beef extract.........................................................3.0g 2,3,5-Triphenyltetrazolium chloride .................0.05g
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into screw-capped tubes in 8.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation, maintenance, and observation of the motility of Listeria monocytogenes.
Motility Test and Maintenance Medium Composition per liter: Agar ....................................................................9.0g Tryptose ..............................................................8.0g NaCl....................................................................5.0g Pancreatic digest of gelatin.................................2.5g Beef extract.........................................................1.5g pH 7.2 ± 0.1 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes in 7.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°– 50°C. Pass the cooled tubes into an anaerobic chamber containing 85% N2 + 10% H2 + 5% CO2.
Use: For the cultivation, maintenance, and observation of the motility in a variety of anaerobic bacteria.
Motility Test and Maintenance Medium Composition per liter: Peptone .............................................................10.0g NaCl....................................................................5.0g Agar ....................................................................4.0g Beef extract.........................................................3.0g pH 7.4 ± 0.1 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix
318
Motility Test and Maintenance Medium, Gilardi
thoroughly. Distribute into screw-capped tubes in 8.0mL volumes. Autoclave for 15 min at 15 psi pressure– 121°C.
2,3,5-Triphenyltetrazolium Chloride Solution: Composition per 10.0mL:
Use: For the cultivation, maintenance, and observa-
2,3,5-Triphenyltetrazolium chloride ...................0.1g
tion of motility in members of the Enterobacteriaceae.
Preparation of 2,3,5-Triphenyltetrazolium Chloride Solution: Add 2,3,5-triphenyltetrazoli-
Motility Test and Maintenance Medium, Gilardi
um chloride to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Composition per liter: Pancreatic digest of casein................................10.0g NaCl ....................................................................5.0g Agar ....................................................................3.0g Yeast extract........................................................3.0g pH 7.2 ± 0.1 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into screw-capped tubes in 3.5mL volumes. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation, maintenance, and observation of motility in nonfermenting Gram–negative bacteria.
Motility Test and Maintenance Medium, Tatum Composition per liter: Tryptose ..............................................................8.0g NaCl ....................................................................5.0g Agar ....................................................................4.0g Pancreatic digest of gelatin .................................2.5g Beef extract .........................................................1.5g pH 6.9 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into screw-capped tubes in 8.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation, maintenance, and observation of motility in nonfermenting Gram–negative bacteria.
Motility Test Medium Composition per liter: Pancreatic digest of gelatin ...............................10.0g NaCl ....................................................................5.0g Agar ....................................................................4.0g Beef extract .........................................................3.0g pH 7.3 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 995.0mL. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 5.0mL of sterile 2,3,5-triphenyltetrazolium chloride solution. Mix thoroughly. Aseptically distribute into sterile tubes.
Use: For detection of the motility of Gram-negative enteric bacteria.
Motility Test Medium Composition per liter: Tryptose ............................................................10.0g NaCl....................................................................5.0g Agar ....................................................................5.0g pH 7.2 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Distribute into tubes in 4–5.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C. Cool tubes quickly in an upright position.
Use: For the determination of bacterial motility.
Motility Test Medium, Semisolid Composition per liter: Peptone .............................................................10.0g NaCl....................................................................5.0g Agar ....................................................................4.0g Beef extract.........................................................3.0g pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Distribute into screw-capped tubes in 8.0mL or 20.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes in 20.0mL volumes or leave in tubes.
Use: For the cultivation and observation of motility in a variety of bacteria, especially Salmonella species.
Mucate Broth
MRS Agar (DeMan, Rogosa, Sharpe Agar)
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MRVP Broth (Methyl Red- Voges-Proskauer Broth)
Composition per liter:
Composition per liter:
Glucose .............................................................18.5g Agar ..................................................................13.5g Pancreatic digest of gelatin ...............................10.0g Beef extract .........................................................8.0g Yeast extract........................................................4.0g Sodium acetate....................................................3.0g K2HPO4 ...............................................................2.0g Ammonium citrate ..............................................2.0g Polysorbate 80.....................................................1.0g MgSO4·7H2O ......................................................0.2g MnSO4·4H2O ....................................................0.05g pH 6.2 ± 0.2 at 25°C
Glucose ...............................................................5.0g KH2PO4...............................................................5.0g Pancreatic digest of casein..................................3.5g Peptic digest of animal tissue .............................3.5g pH 6.9 ± 0.2 at 25°C
Source: This medium is available as a premixed
production (Methyl Red test) and acetoin production (Voges-Proskauer reaction).
powder from BD Diagnostic Systems.
Source: Available as a premixed powder from BD Diagnostic Systems and as a prepared medium from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the differentiation of bacteria based on acid
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the isolation and cultivation of Lactobacillus species from clinical specimens.
MRS Broth (DeMan, Rogosa, Sharpe Broth) Composition per liter: Glucose .............................................................18.5g Pancreatic digest of gelatin ...............................10.0g Beef extract .........................................................8.0g Yeast extract........................................................4.0g Sodium acetate....................................................3.0g K2HPO4 ...............................................................2.0g Ammonium citrate ..............................................2.0g Polysorbate 80.....................................................1.0g MgSO4·7H2O ......................................................0.2g MnSO4·4H2O ....................................................0.05g pH 6.2 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
MRVP Medium (Methyl Red Voges-Proskauer Medium) Composition per liter: Glucose ...............................................................5.0g Peptone ...............................................................5.0g Phosphate buffer .................................................5.0g pH 7.5 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the differentiation of bacteria based on acid production (Methyl Red test) and acetoin production (Voges-Proskauer reaction).
Mucate Broth Composition per liter: Mucic acid ........................................................10.0g Peptone .............................................................10.0g Bromthymol Blue ...........................................0.024g pH 7.4 ± 0.1 at 25°C.
Preparation of Medium: Add components to
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Add 5N NaOH while stirring until mucic acid dissolves. Distribute into screw-capped tubes in 5.0mL volumes. Autoclave for 10 min at 15 psi pressure–121°C.
Use: For the isolation and cultivation of Lactobacil-
Use: For the isolation and cultivation of enteroviru-
lus species from clinical specimens.
lent Escherichia coli and Shigella species.
Preparation of Medium: Add components to
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Mucate Control Broth
Mucate Control Broth Composition per liter:
Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Peptone..............................................................10.0g Bromthymol Blue ...........................................0.024g pH 7.4 ± 0.1 at 25°C
Component B: Composition per 490.0mL:
Preparation of Medium: Add components to
Preparation of Component B: Add hemoglobin
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into screw-capped tubes in 5.0mL volumes. Autoclave for 10 min at 15 psi pressure–121°C.
Use: For the isolation and cultivation of enterovirulent Escherichia coli and Shigella species.
Mueller-Hinton Agar Composition per liter: Beef infusion...................................................300.0g Acid hydrolysate of casein................................17.5g Agar ..................................................................17.0g Starch ..................................................................1.5g pH 7.4 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems and Oxoid Unipath. Preparation of Medium: Add components to distilled/deionized water and bring to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the isolation of pathogenic Neisseria species. For antimicrobial susceptibility testing of a variety of bacterial species. For the cultivation and maintenance of Moraxella osloensis and Neisseria meningitidis.
Mueller-Hinton Agar with IsoVitaleX and Hemoglobin
Hemoglobin ......................................................10.0g to distilled/deionized water and bring to 490.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
IsoVitaleX Enrichment: Composition per liter: Glucose ...........................................................100.0g L-Cysteine·HCl..................................................25.9g L-Glutamine ......................................................10.0g L-Cystine .............................................................1.1g Adenine...............................................................1.0g Nicotinamide adenine dinucleotide ..................0.25g Vitamin B12 .........................................................0.1g Thiamine pyrophosphate ....................................0.1g Guanine·HCl .....................................................0.03g Fe(NO3)3·6H2O.................................................0.02g p-Aminobenzoic acid......................................0.013g Thiamine·HCl ..................................................3.0mg
Source: The supplement solution IsoVitaleX enrichment is available from BD Diagnostic Systems. This enrichment may be replaced by supplement VX from BD Diagnostic Systems.
Preparation of IsoVitaleX Enrichment: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize. Warm to 45°–50°C.
Preparation of Medium: Aseptically combine 490.0mL of component A, 490.0mL of component B, and 20.0mL of IsoVitaleX enrichment. Mix thoroughly. Adjust pH to 6.9. Pour into sterile Petri dishes in 20.0mL volumes.
Composition per liter:
Use: For the isolation and cultivation of Legionella
Component A.............................................. 490.0mL Component B .............................................. 490.0mL IsoVitaleX enrichment .................................. 20.0mL pH 6.9 ± 0.2 at 25°C
pneumophila.
Composition per liter:
Component A: Composition per 490.0mL:
Acid hydrolysate of casein................................17.5g Beef extract.........................................................3.0g Starch ..................................................................1.5g pH 7.3 ± 0.1 at 25°C
Beef infusion...................................................300.0g Acid hydrolysate of casein................................17.5g Agar ..................................................................17.0g Starch ..................................................................1.5g
Preparation of Component A: Add components to distilled/deionized water and bring to 490.0mL. Mix thoroughly. Gently heat and bring to boiling.
Mueller-Hinton Broth
Source: This medium is available as a premixed powder from BD Diagnostic Systems and Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring to 1.0L. Mix thor-
Muller-Kauffmann Tetrathionate Broth oughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 10 min at 10 psi pressure–115°C. Do not overheat.
321
Use: For the cultivation of a wide variety of micro-
Papaic digest of soyabean meal ..........................5.0g NaCl....................................................................5.0g 4-Methylumbelliferyl-β-D-glucuronide ..............0.1g pH 7.3 ± 0.2 at 25°C
organisms. For antimicrobial susceptibility testing.
Source: This medium is available from Fluka, Sigma-Aldrich.
Mueller-Hinton Chocolate Agar Beef infusion...................................................300.0g Acid hydrolysate of casein................................17.5g Agar ..................................................................17.0g Starch ..................................................................1.5g Sheep blood................................................... 50.0mL pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components, except sheep blood, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile sheep blood. Mix thoroughly. Gently heat to 70°C for 10 min. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation and maintenance of Neisseria gonorrhoeae and Neisseria meningitidis. For antimicrobial susceptibility testing of fastidious microorganisms.
Mueller-Hinton II Agar Composition per liter: Acid hydrolysate of casein................................17.5g Agar ..................................................................17.0g Beef extract .........................................................2.0g Starch ..................................................................1.5g pH 7.3 ± 0.1 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components to distilled/deionized water and bring to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For antimicrobial disc diffusion susceptibility testing by the Bauer-Kirby method of a variety of bacteria. This medium supplemented with 5% sheep blood is recommended for use in antimicrobial susceptibility testing of Streptococcus pneumoniae and Haemophilus influenzae.
MUG Tryptone Soya Agar Composition per liter: Agar ..................................................................15.0g Casein enzymic hydrolysate .............................15.0g
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 50°C. Pour into sterile Petri dishes.
Use: For cultivation of fastidious and nonfastidious microorganisms by fluorogenic method.
Muller-Kauffmann Tetrathionate Broth Composition per 1028.0mL: Na2S2O3 ............................................................40.7g CaCO3 ...............................................................25.0g Pancreatic digest of casein..................................7.0g Ox bile ..............................................................4.75g Soya peptone.......................................................2.3g NaCl....................................................................2.3g Iodine solution .............................................. 19.0mL Brilliant Green solution .................................. 9.5mL
Iodine Solution: Composition per 100.0mL: Iodine ................................................................20.0g KI ......................................................................25.0g
Preparation of Iodine Solution: Add the KI to approximately 5.0mL of distilled/deionized water. Mix thoroughly. Add the iodine. Gently heat to dissolve. Bring volume to 100.0mL with distilled/deionized water. Filter sterilize. Brilliant Green Solution: Composition per 100.0mL: Brilliant Green ....................................................0.1g
Preparation of Brilliant Green Solution: Add the Brilliant Green to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Gently heat while stirring and bring to boiling. Continue boiling for 30 min while stirring until dye has dissolved. Filter sterilize. Store protected from light.
Preparation of Medium: Add components, except iodine solution and Brilliant Green solution, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Do not autoclave. Cool to 45°C. Prior to use, add 19.0mL of iodine solution and 9.5mL of Brilliant Green solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
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MWY Medium
Use: For the isolation and cultivation of Salmonella species from specimens with a mixed flora.
Peptone ...............................................................5.0g Beef extract.........................................................3.0g pH 7.9 ± 0.1 at 25°C
MWY Medium (Wadowsky and Yee Medium, Modified)
Preparation of Medium: Add components to
Composition per liter: Agar ..................................................................13.0g Yeast extract......................................................10.0g Glycine................................................................3.0g ACES buffer (2-[(2-Amino-2-oxoethyl)amino]-ethane sulfonic acid) ........................2.0g Charcoal, activated..............................................2.0g α-Ketoglutarate...................................................0.2g Fe4(P2O7)3·9H2O...............................................0.05g Bromcresol Purple ............................................0.01g Bromcresol Blue ...............................................0.01g Antibiotic inhibitor ....................................... 10.0mL L-Cysteine·HCl·H2O solution........................ 10.0mL pH 6.9 ± 0.2 at 25°C
Antibiotic Inhibitor: Composition per 10.0mL: Anisomycin.......................................................0.16g Cefamandole ....................................................4.0mg Vancomycin .....................................................1.0mg Polymyxin B ..............................................130,000U
Preparation of Antibiotic Inhibitor: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. L-Cysteine·HCl·H2O
Solution: Composition per 10.0mL: L-Cysteine·HCl·H2O..........................................0.08g
Preparation of L-Cysteine·HCl·H2O Solution:
Add L-cysteine·HCl·H2O to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except L-cysteine and antibiotic inhibitor, to distilled/ deionized water and bring volume to 980.0mL. Mix thoroughly. Adjust medium to pH 6.9 with 1N KOH. Heat gently and bring to boiling for 1 min. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°– 55°C. Add 10.0mL of the sterile L-cysteine·HCl·H2O solution and 10.0mL of the sterile antibiotic solution. Mix thoroughly. Pour into sterile Petri dishes with constant agitation to keep charcoal in suspension.
Use: For the selective isolation and cultivation of Legionella pneumophila and other Legionella species.
Mycin Assay Agar
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the microbiological assay of antibiotics in pharmaceutical products, body fluids, and other sample materials.
Mycobacterium Agar Composition per liter: Agar ..................................................................12.0g Na2HPO4·12H2O.................................................2.5g Typtic digest of casein ........................................2.0g Proteose peptone no.3.........................................2.0g Yeast extract........................................................2.0g Sodium citrate.....................................................1.5g KH2PO4...............................................................1.0g MgSO4·7H2O ......................................................0.6g Glycerol ........................................................ 50.0mL pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.0. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of Actinomyces israelii, Mycobacterium species, and Nocardia farcinica.
Mycobactin Medium Serum Agar Medium: Composition per liter: Noble agar.........................................................15.0g Casamino acids ...................................................2.5g Na2HPO4, anhydrous ..........................................2.5g Sodium citrate.....................................................1.5g KH2PO4...............................................................1.0g MgSO4·7H2O ......................................................0.6g Asparagine ..........................................................0.3g Crude mycobactin.............................................0.16g Chloramphenicol...............................................0.05g Primaricine (myprozine)...................................0.05g Penicillin .................................................... 100,000U Bovine serum, 56°C-inactivated................. 200.0mL Tween 80 (1% solution)................................ 50.0mL Glycerol ........................................................ 25.0mL pH 7.2 ± 0.2 at 25°C
Composition per liter:
Preparation of Crude Mycobactin: Grow My-
Glucose .............................................................15.0g
cobacterium phlei in 600.0mL of mycobactin pro-
Mycobactosel™ Agar duction broth for 2 weeks at 37°C. Autoclave the culture for 15 min at 15 psi pressure–121°C. Filter the cells and wash with distilled/deionized water. Dry cells under CaCl2. Treat 100.0g of dried culture with three successive acetone extractions—500.0mL of acetone for 30 min in a 1.0L flask fitted with a reflux condenser. Evaporate the acetone to dryness. Extract the residue in a Soxhlet apparatus with petroleum ether for 18–20 hr at 40°–60°C. A hard red residue will remain. Dissolve the residue in warm absolute ethanol. Centrifuge for 30 min at 2250 rpm to remove debris. Evaporate the supernatant to dryness. Grind the residue to a powder of crude mycobactin.
Source: Purified mycobactin is available from Allied Labs, Inc., 2520 Hunt St., Ames, IA 50010.
Mycobactin Production Broth: Composition per 600.0mL: Solution B ................................................... 500.0mL Solution A ................................................... 100.0mL
Preparation of Mycobactin Production Broth: Aseptically mix the cooled sterile solution A and solution B.
Solution A: Composition per 100.0mL:
323
Mycobactosel™ Agar Composition per liter: Agar ..................................................................13.5g Bovine albumin fraction V .................................5.0g Glucose ...............................................................2.0g Na2HPO4 .............................................................1.5g KH2PO4...............................................................1.5g Pancreatic digest of casein..................................1.0g NaCl..................................................................0.85g (NH4)2SO4 ..........................................................0.5g Monosodium glutamate ......................................0.5g Sodium citrate.....................................................0.4g MgSO4·7H2O ....................................................0.05g Ferric ammonium citrate...................................0.04g Pyridoxine........................................................1.0mg ZnSO4·7H2O ....................................................1.0mg CuSO4·5H2O ....................................................1.0mg Biotin ...............................................................0.5mg CaCl2·H2O .......................................................0.5mg Malachite Green.............................................0.25mg Antibiotic solution ........................................ 10.0mL Catalase solution........................................... 10.0mL Glycerol .......................................................... 5.0mL Oleic acid ...................................................... 0.06mL pH 6.6 ± 0.2 at 25°C
L-Asparagine .......................................................5.0g
Source: This medium is available as a prepared me-
Na2HPO4 .............................................................2.0g KH2PO4 ...............................................................1.0g Glycerol ........................................................ 30.0mL
dium from BD Diagnostic Systems.
Preparation of Solution A: Add components to
Cycloheximide..................................................0.36g Nalidixic acid....................................................0.02g Lincomycin ......................................................2.0mg
distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Antibiotic Solution: Composition per 10.0mL:
Preparation of Antibiotic Solution: Add com-
Solution B: Composition per 500.0mL:
ponents to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Glucose .............................................................10.0g MgSO4··7H2O .....................................................0.2g
Catalase Solution: Composition per 10.0mL:
Preparation of Solution B: Add components to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Catalase............................................................3.0mg
Preparation of Medium: Add components, ex-
Preparation of Medium: Add components, ex-
cept penicillin, chloramphenicol, primaricine, and bovine serum, to distilled/deionized water and bring volume to 800.0mL. Mix thoroughly. Gently heat with a minimum of heat. Autoclave for 15 min at 10 psi pressure–116°C. Cool to 50°C. Aseptically add penicillin, chloramphenicol, primaricine, and sterile bovine serum. Mix thoroughly. Adjust pH to 7.2. Distribute into sterile tubes or flasks.
cept antibiotic solution and catalase solution, to distilled/deionized water and bring volume to 980.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile antibiotic solution and sterile catalase solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation and maintenance of Mycobac-
Use: For the selective isolation of mycobacteria
terium avium and Mycobacterium paratuberculosis.
from specimens containing mixed flora.
Preparation of Catalase Solution: Add catalase to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
324
Mycobactosel L-J Medium
Mycobactosel L-J Medium Composition per liter: Potato flour .......................................................30.0g L-Asparagine .......................................................3.6g KH2PO4, anhydrous ............................................2.5g Sodium citrate .....................................................0.6g MgSO4·7H2O ....................................................0.24g Homogenized whole egg ................................... 1.0L Malachite Green solution.............................. 20.0mL Glycerol ........................................................ 12.0mL Antibiotic solution ........................................ 10.0mL pH 7.0 ± 0.2 at 25°C
Source: This medium is available as a prepared medium from BD Diagnostic Systems.
Homogenized Whole Egg: Composition per liter: Whole eggs ......................................................18–24
Preparation of Whole Egg: Use fresh eggs, less than 1 week old. Scrub the shells with soap. Let stand in a soap solution for 30 min. Rinse in running water. Soak eggs in 70% ethanol for 15 min. Break the eggs into a sterile container. Homogenize by shaking. Filter through four layers of sterile cheesecloth into a sterile graduated cylinder. Measure out 1.0L.
Malachite Green Solution: Composition per 20.0mL: Malachite Green..................................................0.4g
Preparation of Malachite Green Solution: Add Malachite Green to sterile distilled/deionized water and bring volume to 20.0mL in a sterile container. Mix thoroughly.
Antibiotic Solution: Composition per 10.0mL: Cycloheximide ..................................................0.64g Nalidixic acid ..................................................0.056g Lincomycin ......................................................3.2mg
Preparation of Antibiotic Solution: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components—except whole egg, Malachite Green solution, and antibiotic solution—to distilled/deionized water and bring volume to 600.0mL. Mix thoroughly. Autoclave for 30 min at 15 psi pressure–121°C. Cool to room temperature. Add the homogenized whole egg, Malachite Green solution, and antibiotic solution. Distribute into sterile tubes in 8.0mL volumes. Coagulate medium in a slanted position at 85°C (moist heat) for 50 min.
Use: For the isolation and cultivation of Mycobacterium species from clinical specimens.
Mycobiotic Agar (Cycloheximide Chloramphenicol Agar) Composition per liter: Agar ..................................................................15.0g Enzymatic hydrolysate of soybean meal ..........10.0g Glucose .............................................................10.0g Cycloheximide....................................................0.5g Chloramphenicol...............................................0.05g pH 6.5 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Cool tubes quickly in a slanted position.
Use: For the selective isolation and cultivation of pathogenic fungi.
Mycological Agar Composition per liter: Agar ..................................................................15.0g Enzymatic hydrolysate of soybean meal ..........10.0g Glucose .............................................................10.0g pH 7.0 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the selective isolation, cultivation, and maintenance of pathogenic fungi.
Mycological Agar with Low pH Composition per liter: Agar ..................................................................15.0g Enzymatic hydrolysate of soybean meal ..........10.0g Glucose .............................................................10.0g pH 4.8 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Mycoplasma Agar Use: For the selective isolation, cultivation, and maintenance of pathogenic fungi.
Mycological Broth Composition per liter: Glucose .............................................................40.0g Enzymatic hydrolysate of soybean meal ..........10.0g pH 7.0 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of fungi.
Mycophil™ Broth Composition per liter: Glucose .............................................................40.0g Pancreatic digest of casein..................................5.0g Peptic digest of animal tissue..............................5.0g pH 7.0 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–118°C. Do not overheat.
Use: For the isolation and cultivation of a wide variety of fungi.
Mycoplasma Agar (ATCC Medium 555) Composition per 103.0mL:
325
Preparation of Hartley’s Digest Broth: Finely mince the ox heart. Add the meat to 5.0L of distilled/ deionized water. Gently heat and bring to 80°C. Add the 5.0L of Na2CO3 solution. Cool to 45°C. Add pancreatin and maintain at 45°C for 4 hr while stirring. Add the HCl and steam at 100°C for 30 min. Cool to room temperature. Adjust pH to 8.0 with 1N NaOH. Gently heat and bring to boiling. Continue boiling for 25 min. Filter while hot. Cool to room temperature. Adjust pH to 7.5. Autoclave for 15 min at 15 psi pressure–121°C. Pig Serum: Composition per 100.0mL: Pig serum .................................................... 100.0mL
Preparation of Pig Serum: Adjust pH of pig serum to 4.4 with sterile 1N HCl. Do not let pH go below 4.2. Let serum stand at 4°C for 18-20h. Adjust pH to 7.0 with sterile 1N NaOH. Centrifuge at 9000 rpm for 20 min. Discard pellet. Filter supernatant solution through a 0.2µm membrane. Store at −70°C.
Enzymatic Hydrolysate of Lactalbumin: Composition per 100.0mL: Enzymatic hydrolysate of lactalbumin ...............5.0g
Preparation of Enzymatic Hydrolysate of Lactalbumin: Add enzymatic hydrolysate of lactalbumin to 100.0mL of phosphate buffered saline, 1X, pH 7.0.
Phosphate Buffered Saline Solution, 1X: Composition per liter: NaCl....................................................................8.0g Na2HPO4·7H2O.................................................2.16g KCl......................................................................0.2g KH2PO4...............................................................0.2g MgCl2·6H2O .......................................................0.1g CaCl2 ...................................................................0.1g
Hanks’ Balanced Salt Solution, 10X: Composition per liter:
Noble agar...........................................................0.7g Hartley’s digest broth.................................... 30.0mL Pig serum ...................................................... 20.0mL Enzymatic hydrolysate of lactalbumin ......... 10.0mL Hanks’ balanced salt solution, 10X ................ 4.0mL Fresh yeast extract solution............................. 2.0mL Phenol Red (0.25% solution) .......................... 1.0mL pH 7.4 ± 0.2 at 25°C
NaCl..................................................................80.0g Glucose .............................................................10.0g KCl......................................................................4.0g CaCl2 ...................................................................1.4g MgCl2·6H2O .......................................................1.0g MgSO4·7H2O ......................................................1.0g Na2HPO4·7H2O...................................................0.9g KH2PO4...............................................................0.6g
Hartley’s Digest Broth: Composition per 10.0L:
Preparation of Hanks’ Balanced Salt Solution, 10X: Add components to distilled/deionized
Ox heart........................................................3,000.0g Pancreatin..........................................................50.0g Na2CO3 , anhydrous (0.8% solution) ................. 5.0L HCl, concentrated ......................................... 80.0mL pH 7.5 ± 0.2 at 25°C
water and bring volume to 1.0L. Mix thoroughly.
Preparation of Medium: Combine components, except agar, in the following order: Hanks’ balanced salt solution, 10X, Phenol Red, Hartley’s digest broth, pig serum, enzymatic hydrolysate of lactalbu-
326
Mycoplasma Agar Base
min, and fresh yeast extract solution. Mix thoroughly. Adjust pH to 7.4 with 1N NaOH. Filter sterilize through a 0.2µm membrane. Add 0.7g of Noble agar to 36.0mL of distilled/deionized water. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 56°C. Warm basal medium to 56°C. Aseptically combine the two solutions. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation of Mycoplasma species.
Mycoplasma Agar Base (PPLO Agar Base) Composition per 1300.0mL: Agar ..................................................................14.0g Pancreatic digest of casein..................................7.0g NaCl ....................................................................5.0g Beef extract .........................................................3.0g Yeast extract........................................................3.0g Beef heart, solids from infusion..........................2.0g Horse serum ................................................ 260.0mL Fresh yeast extract solution........................... 65.0mL pH 7.8 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Fresh Yeast Extract Solution: Composition per 100.0mL: Baker’s yeast, live, pressed, starch-free............25.0g
Yeast extract........................................................3.0g Beef heart, solids from infusion..........................2.0g Thallous acetate ..................................................0.7g Penicillin ...................................................... 70,000U Horse serum ................................................ 260.0mL Fresh yeast extract solution .......................... 65.0mL pH 7.8 ± 0.2 at 25°C
Caution: Thallous acetate is a poison. Fresh Yeast Extract Solution: Composition per 100.0mL: Baker’s yeast, live, pressed, starch-free............25.0g
Preparation of Fresh Yeast Extract Solution: Add the live Baker’s yeast to 100.0mL of distilled/ deionized water. Autoclave for 90 min at 15 psi pressure–121°C. Allow to stand. Remove supernatant solution. Adjust pH to 6.6–6.8. Preparation of Medium: Add components—except horse serum, special yeast extract, thallous acetate, and penicillin—to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C. To each of 70.0mL of cooled, sterile basal medium, add 20.0mL of sterile horse serum, 10.0mL of special yeast extract, 50.0mg of thallous acetate, and 5000U of penicillin. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Preparation of Fresh Yeast Extract Solution: Add the live Baker’s yeast to 100.0mL of distilled/ deionized water. Autoclave for 90 min at 15 psi pressure–121°C. Allow to stand. Remove supernatant solution. Adjust pH to 6.6–6.8.
Use: For the preparation of media for the cultivation
Preparation of Medium: Add components, ex-
Agar ..................................................................10.0g Bacteriological peptone ....................................10.0g Beef extract.......................................................10.0g NaCl....................................................................5.0g Special mineral supplement................................0.5g Mycoplasma supplement G......................... 250.0mL pH 7.8 ± 0.2 at 25°C
cept horse serum and fresh yeast extract, to distilled/ deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C. To each 75.0mL of cooled, sterile basal medium, add 20.0mL of sterile horse serum and 5.0mL of special yeast extract. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the preparation of media for the cultivation of Mycoplasma.
Mycoplasma Agar with Increased Selectivity Composition per 1300.0mL: Agar ..................................................................14.0g Pancreatic digest of casein..................................7.0g NaCl ....................................................................5.0g Beef extract .........................................................3.0g
of Mycoplasma species.
Mycoplasma Agar with Supplement G Composition per liter:
Source: This medium is available as a premixed powder from Oxoid Unipath.
Mycoplasma Supplement G: Composition per 20.0mL: Thallous acetate .............................................25.0mg Horse serum .................................................. 20.0mL Yeast extract (25% solution)......................... 10.0mL Penicillin ...................................................... 20,000U
Preparation of Mycoplasma Supplement G: Add components to distilled/deionized water and bring volume to 20.0mL. Mix thoroughly. Filter sterilize.
Caution: Thallous acetate is a poison.
Mycoplasma Broth Preparation of Medium: Add components, except Mycoplasma supplement G, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into flasks in 80.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C. Aseptically add 20.0mL of sterile Mycoplasma supplement G to each 80.0mL of basal medium. Mix thoroughly.
Use: For the growth of Mycoplasma species.
Mycoplasma Agar with Supplement P Composition per liter:
327
Use: For the growth of Mycoplasma species.
Mycoplasma Broth (ATCC Medium 555) Composition per 103.0mL: Hartley’s digest broth.................................... 30.0mL Pig serum ...................................................... 20.0mL Enzymatic hydrolysate of lactalbumin ......... 10.0mL Hanks’ balanced salt solution, 10X ................ 4.0mL Fresh yeast extract solution ............................ 2.0mL Phenol Red (0.25% solution).......................... 1.0mL pH 7.4 ± 0.2 at 25°C
Agar ..................................................................10.0g Bacteriological peptone ....................................10.0g Beef extract .......................................................10.0g NaCl ....................................................................5.0g Special mineral supplement ................................0.5g Mycoplasma supplement P ......................... 250.0mL pH 7.8 ± 0.2 at 25°C
Hartley’s Digest Broth: Composition per 10.0L:
Source: This medium is available as a premixed powder from Oxoid Unipath.
Preparation of Hartley’s Digest Broth: Finely mince the ox heart. Add the meat to 5.0L of distilled/ deionized water. Gently heat and bring to 80°C. Add the 5.0L of Na2CO3 solution. Cool to 45°C. Add pancreatin and maintain at 45°C for 4 hr while stirring. Add the HCl and steam at 100°C for 30 min. Cool to room temperature. Adjust pH to 8.0 with 1N NaOH. Gently heat and bring to boiling. Continue boiling for 25 min. Filter while hot. Cool to room temperature. Adjust pH to 7.5. Autoclave for 15 min at 15 psi pressure–121°C.
Mycoplasma Supplement P: Composition per 20.0mL: Glucose ...............................................................0.3g Mycoplasma broth base ..................................0.145g Thallous acetate ...............................................8.0mg Phenol Red.......................................................1.2mg Methylene Blue chloride..................................0.3mg Penicillin ......................................................12,000U Horse serum .................................................... 6.0mL Yeast extract (25% solution) ........................... 3.0mL
Preparation of Mycoplasma Supplement P: Add components to distilled/deionized water and bring volume to 20.0mL. Mix thoroughly. Filter sterilize.
Caution: Thallous acetate is a poison. Fresh Yeast Extract Solution: Composition per 100.0mL: Baker’s yeast, live, pressed, starch-free............25.0g
Preparation of Fresh Yeast Extract Solution: Add the live Baker’s yeast to 100.0mL of distilled/ deionized water. Autoclave for 90 min at 15 psi pressure–121°C. Allow to stand. Remove supernatant solution. Adjust pH to 6.6–6.8.
Preparation of Medium: Add components, except Mycoplasma supplement P, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into bottles in 1.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C. Cool to room temperature. Aseptically add 2.0mL of sterile Mycoplasma supplement P to each bottle.
Ox heart .......................................................3,000.0g Pancreatin .........................................................50.0g Na2CO3 , anhydrous (0.8% solution) ................. 5.0L HCl, concentrated ......................................... 80.0mL pH 7.5 ± 0.2 at 25°C
Pig Serum: Composition per 100.0mL: Pig serum .................................................... 100.0mL
Preparation of Pig Serum: Adjust pH of pig serum to 4.4 with sterile 1N HCl. Do not let pH go below 4.2. Let serum stand at 4°C for 18-20h. Adjust pH to 7.0 with sterile 1N NaOH. Centrifuge at 9000 rpm for 20 min. Discard pellet. Filter supernatant solution through a 0.2µm membrane. Store at −70°C.
Enzymatic Hydrolysate of Lactalbumin: Composition per 100.0mL: Enzymatic hydrolysate of lactalbumin ...............5.0g
Preparation of Enzymatic Hydrolysate of Lactalbumin: Add enzymatic hydrolysate of lactalbumin to 100.0mL of phosphate buffered saline, 1X, pH 7.0.
Phosphate Buffered Saline Solution, 1X: Composition per liter: NaCl....................................................................8.0g Na2HPO4·7H2O.................................................2.16g KCl......................................................................0.2g KH2PO4...............................................................0.2g
328
Mycoplasma Broth Base
MgCl2·6H2O .......................................................0.1g CaCl2 ...................................................................0.1g
Preparation of Buffered Saline Solution, 1X: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly.
Hanks’ Balanced Salt Solution, 10X: Composition per liter: NaCl ..................................................................80.0g Glucose .............................................................10.0g KCl......................................................................4.0g CaCl2 ...................................................................1.4g MgCl2·6H2O .......................................................1.0g MgSO4·7H2O ......................................................1.0g Na2HPO4·7H2O...................................................0.9g KH2PO4 ...............................................................0.6g
Preparation of Hanks’ Balanced Salt Solution, 10X: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly.
Preparation of Medium: Combine components in the following order: Hanks’ balanced salt solution, 10X, Phenol Red, Hartley’s digest broth, pig serum, enzymatic hydrolysate of lactalbumin, and fresh yeast extract solution. Mix thoroughly. Add 36.0mL of distilled/deionized water. Adjust pH to 7.4 with 1N NaOH. Filter sterilize through a 0.2µm membrane. Store at 4°C for up to 3 weeks.
NaCl....................................................................5.0g Beef extract.........................................................3.0g Yeast extract........................................................3.0g Beef heart, solids from infusion..........................2.0g Horse serum ................................................ 260.0mL Fresh yeast extract solution .......................... 65.0mL pH 7.8 ± 0.2 at 25°C
Fresh Yeast Extract Solution: Composition per 100.0mL: Baker’s yeast, live, pressed, starch-free............25.0g
Preparation of Fresh Yeast Extract Solution: Add the live Baker’s yeast to 100.0mL of distilled/ deionized water. Autoclave for 90 min at 15 psi pressure–121°C. Allow to stand. Remove supernatant solution. Adjust pH to 6.6–6.8. Preparation of Medium: Add components, except horse serum and fresh yeast extract, to distilled/ deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C. To each 75.0mL of cooled, sterile basal medium, add 20.0mL of sterile horse serum and 5.0mL of fresh yeast extract. Mix thoroughly. Aseptically distribute into sterile tubes.
Use: For the isolation and cultivation of Mycoplasma species.
Use: For the cultivation of Mycoplasma species.
Mycoplasma Broth with Supplement G Mycoplasma Broth Base (PPLO Broth Base without Crystal Violet) Composition per liter: Pancreatic digest of casein..................................7.0g NaCl ....................................................................5.0g Beef extract .........................................................3.0g Yeast extract........................................................3.0g Beef heart, solids from infusion..........................2.0g pH 7.8 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Gently heat and bring to boiling. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: Used as a basal medium that should be enriched for the isolation and cultivation of Mycoplasma species.
Composition per liter: Bacteriological peptone ....................................10.0g Beef extract.......................................................10.0g NaCl....................................................................5.0g Special mineral supplement, Oxoid Unipath ......0.5g Mycoplasma supplement G......................... 250.0mL pH 7.8 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath.
Mycoplasma Supplement G: Composition per 20.0mL: Thallous acetate .............................................25.0mg Horse serum .................................................. 20.0mL Yeast extract (25% solution)......................... 10.0mL Penicillin ...................................................... 20,000U
Preparation of Mycoplasma Supplement G: Add components to distilled/deionized water and bring volume to 20.0mL. Mix thoroughly. Filter sterilize.
Caution: Thallous acetate is a poison.
Mycoplasma Broth, Supplemented Composition per liter: Pancreatic digest of casein..................................7.0g
Preparation of Medium: Add components, except Mycoplasma supplement G, to distilled/deionized water and bring volume to 1.0L. Mix
Mycoplasma pneumoniae Isolation Medium thoroughly. Gently heat and bring to boiling. Distribute into flasks in 80.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C. Aseptically add 20.0mL of sterile Mycoplasma supplement G to each 80.0mL of basal medium. Mix thoroughly.
Use: For the growth of Mycoplasma species.
Mycoplasma Broth with Supplement P Composition per liter: Bacteriological peptone ....................................10.0g Beef extract .......................................................10.0g NaCl ....................................................................5.0g Special mineral supplement, Oxoid Unipath ......0.5g Mycoplasma supplement P ......................... 250.0mL pH 7.8 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath.
Mycoplasma Supplement P: Composition per 20.0mL: Glucose ...............................................................0.3g Mycoplasma broth base ..................................0.145g Thallous acetate ...............................................8.0mg Phenol Red.......................................................1.2mg Methylene Blue chloride..................................0.3mg Penicillin ......................................................12,000U Horse serum .................................................... 6.0mL Yeast extract (25% solution) ........................... 3.0mL
Preparation of Mycoplasma Supplement P: Add components to distilled/deionized water and bring volume to 20.0mL. Mix thoroughly. Filter sterilize.
Caution: Thallous acetate is a poison. Preparation of Medium: Add components, except Mycoplasma supplement P, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into bottles in 1.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C. Cool to room temperature. Aseptically add 2.0mL of sterile Mycoplasma supplement P to each bottle.
Use: For the cultivation of Mycoplasma species.
Mycoplasma Horse Serum Broth (ATCC Medium 1959) Mycoplasma broth base .............................. 660.0mL Horse serum ................................................ 200.0mL Yeast extract solution .................................. 100.0mL Phenol Red (0.1%)........................................ 20.0mL Glucose solution ........................................... 10.0mL NaOH (1N solution)...................................... 6.25mL Arginine solution ............................................ 5.0mL
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Mycoplasma Broth Base: Composition per liter: Pancreatic digest of casein..................................7.0g NaCl....................................................................5.0g Beef extract.........................................................3.0g Yeast extract........................................................3.0g Beef heart, solids from infusion..........................2.0g
Preparation of Mycoplasma Broth Base: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Yeast Extract Solution: Composition per 100.0mL: Baker’s yeast, live, pressed, starch-free............25.0g
Preparation of Fresh Yeast Extract Solution: Add the live Baker’s yeast to 100.0mL of distilled/ deionized water. Autoclave for 90 min at 15 psi pressure–121°C. Allow to stand. Remove supernatant solution. Adjust pH to 6.6–6.8. Glucose Solution: Composition per 10.0mL: Glucose ...............................................................5.0g
Preparation of Glucose Solution: Add glucose to 10.0mL of distilled/deionized water. Mix thoroughly. Filter sterilize.
Arginine Solution: Composition per 10.0mL: L-Arginine...........................................................4.2g
Preparation of Arginine Solution: Add arginine to 10.0mL of distilled/deionized water. Mix thoroughly. Filter sterilize.
Preparation of Medium: Combine 660.0mL Mycoplasma broth base, 20.0mL Phenol Red, and 6.25mL 1N NaOH. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C. Aseptically add 5.0mL sterile arginine solution, 100.0mL sterile yeast extract solution, 10.0mL sterile glucose solution, and 200.0mL filter sterilized horse serum. Mix thoroughly. Aseptically distribute into sterile tubes or flasks. Use: For the preparation of media for the cultivation of Mycoplasma spp.
Mycoplasma pneumoniae Isolation Medium Composition per 1200.0mL: Beef heart for infusion ......................................50.0g Peptone .............................................................10.0g NaCl....................................................................5.0g Water........................................................... 900.0mL
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Mycoplasmal Agar
Yeast extract solution .................................. 100.0mL α-Gamma horse serum, unheated ............... 200.0mL pH 7.6–7.8 at 25°C
Carbohydrate Solution: Composition per 50.0mL:
Yeast Extract Solution: Composition per 10.0mL:
Preparation of Carbohydrate Solution: Add
Yeast, active dry Baker’s ................................250.0g
Preparation of Yeast Extract Solution: Add yeast to 1.0L of distilled/deionized water. Mix thoroughly. Gently heat and bring to boiling. Filter through Whatman no. 2 filter paper. Adjust the pH of the filtrate to 8.0 with NaOH. Distribute into tubes in 10.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C. Store at −20°C.
Preparation of Medium: Add components, ex-
cept yeast extract solution and α-gamma horse serum, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C. Aseptically add sterile yeast extract solution and α-gamma horse serum. Mix thoroughly. Aseptically distribute into sterile tubes.
Use: For the isolation and cultivation of Mycoplasma pneumoniae.
Mycoplasmal Agar Composition per liter: Papaic digest of soy meal..................................20.0g Agarose .............................................................10.0g NaCl ....................................................................5.0g Phenol Red (2% solution) ............................... 1.0mL pH 7.3 ± 0.2 at 25°C
Preparation of Medium: Add components, except agarose, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.3 with 1N NaOH. Add agarose. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure– 121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the isolation and cultivation of human mycoplasmas and ureaplasmas.
Neisseria Medium Composition per liter: Biosate ..............................................................10.0g Polypeptone ......................................................10.0g NaCl ....................................................................5.0g Myosate...............................................................3.0g Agar ....................................................................1.5g Phenol Red......................................................0.017g Carbohydrate solution................................... 50.0mL pH 7.4–7.6 at 25°C
Carbohydrate.....................................................10.0g glucose, sucrose, or maltose to distilled/deionized water and bring volume to 50.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except carbohydrate solution, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile carbohydrate solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation of Neisseria species.
Neisseria meningitidis Medium Composition per liter: Beef infusion...................................................300.0g Acid hydrolysate of casein................................17.5g Agar ..................................................................17.0g Starch ..................................................................1.5g Antibiotic solution ........................................ 10.0mL pH 7.4 ± 0.2 at 25°C
Antibiotic Solution: Composition per 10.0mL: Vancomycin .....................................................3.0mg Colistin.............................................................7.5mg Nystatin........................................................ 12,500U
Preparation of Antibiotic Solution: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except antibiotic solution, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile antibiotic solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the selective isolation and cultivation of Neisseria meningitidis.
Nelson Culture Medium for Naegleria Composition per 100.0mL: Glucose .............................................................0.17g Panmede............................................................0.17g Na2HPO4 ........................................................14.2mg KH2PO4..........................................................13.6mg NaCl...............................................................12.0mg CaCl2·2H2O .....................................................0.4mg MgSO4·7H2O ...................................................0.4mg Bovine serum, heat-inactivated fetal ............ 10.0mL
Neomycin Blood Agar Source: Panmede is available from Paines and Byrne Ltd., Greenford, England, and Harrisons and Crosfield, Inc., Bronxville, NY.
Preparation of Medium: Add components, except bovine serum, to distilled/deionized water and bring volume to 90.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C. Aseptically add 10.0mL of sterile, heat-inactivated fetal bovine serum. Mix thoroughly. Aseptically distribute into sterile tubes or flasks. Use immediately.
Use: For the cultivation of Naegleria fowleri and Paratetramitus jugosus.
Nelson Culture Medium for Naegleria Composition per 100.0mL: Glucose .............................................................0.17g Liver infusion....................................................0.17g Na2HPO4 ........................................................14.2mg KH2PO4 ..........................................................13.6mg NaCl ...............................................................12.0mg CaCl2·2H2O......................................................0.4mg MgSO4·7H2O ...................................................0.4mg Bovine serum, heat-inactivated fetal ............ 10.0mL
Preparation of Medium: Add components, except bovine serum, to distilled/deionized water and bring volume to 90.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C. Aseptically add 10.0mL of sterile, heat-inactivated fetal bovine serum. Mix thoroughly. Aseptically distribute into sterile tubes or flasks. Use immediately.
Use: For the cultivation of Naegleria fowleri and Paratetramitus jugosus.
Nelson Medium for Naegleria fowleri Composition per liter: Glucose ...............................................................1.0g Ox liver digest.....................................................1.0g Page’s amoeba saline ......................................... 1.0L Fetal calf serum, inactivated ......................... 20.0mL
Page’s Amoeba Saline: Composition per liter: Na2HPO4 .........................................................0.142g KH2PO4 ...........................................................0.136g NaCl ..................................................................0.12g MgSO4·7H2O ...................................................4.0mg CaCl2·2H2O......................................................4.0mg
Preparation of Page’s Amoeba Saline: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Preparation of Medium: Add the glucose and ox liver digest to 1.0L of Page’s amoeba saline. Mix thoroughly. Distribute into screw-capped tubes in
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10.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C. Aseptically add 0.2mL of sterile fetal calf serum to each tube. Mix thoroughly.
Use: For the cultivation of Naegleria fowleri.
Neomycin Agar, Modified Composition per liter: Agar ..................................................................15.0g Peptone ...............................................................6.0g Pancreatic digest of casein..................................4.0g Yeast extract........................................................3.0g Beef extract.........................................................1.5g Glucose ...............................................................1.0g Methanol ....................................................... 20.0mL Neomycin solution........................................ 10.0mL pH 7.0 ± 0.2 at 25°C
Neomycin Solution: Composition per 10.0mL: Neomycin sulfate ................................................1.0g
Preparation of Neomycin Solution: Add neomycin sulfate to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except methanol and neomycin solution, to distilled/ deionized water and bring volume to 970.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Filter sterilize methanol. To cooled, sterile basal medium, aseptically add sterile methanol and sterile neomycin solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation and maintenance of Bordetella bronchiseptica.
Neomycin Blood Agar Composition per liter: Pancreatic digest of casein................................14.5g Agar ..................................................................14.0g Papaic digest of soybean meal............................5.0g NaCl....................................................................5.0g Growth factors ....................................................1.5g Sheep blood, defibrinated ............................. 50.0mL Neomycin solution........................................ 10.0mL pH 7.3 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Neomycin Solution: Composition per 10.0mL: Neomycin sulfate ..............................................0.03g
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Neomycin Luria Agar
Preparation of Neomycin Solution: Add neomycin sulfate to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except sheep blood and neomycin solution, to distilled/ deionized water and bring volume to 940.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile sheep blood and sterile neomycin solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation and cultivation of group A streptococci (Streptococcus pyogenes) and group B streptococci (Streptococcus agalactiae) from throat cultures and other clinical specimens.
NaCl....................................................................5.0g Yeast extract........................................................2.0g Beef extract.........................................................1.0g Sucrose solution............................................ 20.0mL Neomycin...................................................... 10.0mL pH 7.0 ± 0.1 at 25°C
Sucrose Solution: Composition per 100.0mL: Sucrose................................................................2.5g
Preparation of Sucrose Solution: Add sucrose to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Neomycin Solution: Composition per 10.0mL: Neomycin sulfate .........................................500.0mg
Neomycin Luria Agar Composition per liter: Agar ..................................................................15.0g Pancreatic digest of casein................................10.0g Yeast extract........................................................5.0g NaCl ....................................................................0.5g Glucose solution ........................................... 20.0mL Neomycin...................................................... 10.0mL pH 7.0 ± 0.1 at 25°C
Preparation of Neomycin Solution: Add neomycin sulfate to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except
Glucose Solution: Composition per 100.0mL:
sucrose solution and neomycin solution, to distilled/ deionized water and bring volume to 970.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Aseptically add 20.0mL of sterile sucrose solution and 10.0mL of sterile neomycin solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Glucose .............................................................10.0g
Use: For the cultivation of Pseudomonas aerugi-
Preparation of Glucose Solution: Add glucose
nosa.
to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Neomycin Solution: Composition per 10.0mL: Neomycin sulfate ...........................................12.0mg
Preparation of Neomycin Solution: Add neomycin sulfate to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except glucose solution and neomycin solution, to distilled/ deionized water and bring volume to 970.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Aseptically add 20.0mL of sterile glucose solution and 10.0mL of sterile neomycin solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation of Escherichia coli.
Neomycin Medium No. 1 Composition per liter: Agar ..................................................................15.0g Peptone................................................................5.0g
Neopeptone Glucose Agar Composition per liter: Agar ..................................................................20.0g Glucose .............................................................10.0g Neopeptone .........................................................5.0g pH 6.5 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Adjust pH to 6.5. Pour into sterile Petri dishes or leave in tubes.
Use: For the maintenance of stock cultures of a variety of microorganisms.
Neopeptone Glucose Rose Bengal Aureomycin® Agar Composition per liter: Agar ..................................................................20.0g Neopeptone .........................................................5.0g Glucose ...............................................................1.0g
New York City Medium
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Tetracycline solution....................................... 5.0mL Rose Bengal solution ...................................... 3.5mL pH 6.5 ± 0.2 at 25°C
Glucose solution ........................................... 10.0mL Antibiotic VCNT solution .............................. 5.0mL pH 7.4 ± 0.2 at 25°C
Tetracycline Solution: Composition per 150.0mL:
NYC Basal Medium: Composition per 640.0mL:
Tetracycline.........................................................1.0g
Preparation of Tetracycline Solution: Add tetracycline to distilled/deionized water and bring volume to 150.0mL. Mix thoroughly. Filter sterilize.
Rose Bengal Solution: Composition per 100.0mL: Rose Bengal ........................................................1.0g
Preparation of Rose Bengal Solution: Add Rose Bengal to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except tetracycline solution, to distilled/deionized water and bring volume to 995.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 5.0mL of sterile tetracycline solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation and cultivation of a wide variety of fungal species.
Neopeptone Infusion Agar Composition per liter: Beef heart, infusion from ................................500.0g Neopeptone .......................................................20.0g Agar ..................................................................20.0g NaCl ....................................................................5.0g Sheep blood, defibrinated ............................. 50.0mL pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components, except sheep blood, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile sheep blood. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation of a wide variety of fastidious microorganisms.
Solution 1.................................................... 400.0mL Solution 3.................................................... 200.0mL Solution 2...................................................... 40.0mL
Preparation of NYC Basal Medium: Combine solution 1, solution 2, and solution 3. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Solution 1: Composition per 400.0mL: Agar ..................................................................20.0g
Preparation of Solution 1: Add agar to distilled/ deionized water and bring volume to 400.0mL. Mix thoroughly. Melt agar in autoclave for 10 min at 0 psi pressure–100°C. Cool to 45°–50°C.
Solution 2: Composition per 40.0mL: Cornstarch...........................................................1.0g
Preparation of Solution 2: Add cornstarch to distilled/deionized water and bring volume to 40.0mL. Mix thoroughly. Warm to 45°–50°C. Solution 3: Composition per 200.0mL: Proteose peptone no. 3......................................15.0g NaCl....................................................................5.0g K2HPO4...............................................................4.0g KH2PO4...............................................................1.0g
Preparation of Solution 3: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Cool to 45°–50°C.
Horse Blood Cells: Composition per 200.0mL: Horse blood cells, sedimented ........................ 6.0mL
Preparation of Horse Blood Cells: Cow blood may be used instead of horse blood but do not use sheep blood. Use cells freshly packed by sedimentation. Do not pack by centrifugation. Aseptically add 6.0mL of sedimented blood cells to 200.0mL of sterile distilled/deionized water. Mix thoroughly.
Composition per liter:
Horse Plasma, Citrated: Composition per 6.0L:
NYC basal medium..................................... 640.0mL Horse blood cells ........................................ 200.0mL Horse plasma, citrated................................. 120.0mL Yeast dialysate............................................... 25.0mL
Preparation of Horse Plasma, Citrated: Place 600.0mL of sterile citrate solution into a receiving
New York City Medium
Horse blood............................................... 5400.0mL Citrate solution............................................ 600.0mL
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New York City Medium, Modified
bottle. Draw horse blood to the 6.0L mark. Allow cells to sediment out. Aseptically remove plasma.
Citrate Solution: Composition per liter: Sodium citrate .................................................150.0g NaCl ................................................................81.13g
Preparation of Citrate Solution: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
Glucose Solution: Composition per 10.0mL: D-Glucose ............................................................5.0g
Preparation of Glucose Solution: Add
Glucose solution ........................................... 10.0mL Antibiotic LCNT solution............................... 5.0mL pH 7.4 ± 0.2 at 25°C
NYC Basal Medium: Composition per 840.0mL: Horse blood............................................... 5400.0mL Solution 1.................................................... 600.0mL Solution 3.................................................... 200.0mL Solution 2...................................................... 40.0mL
Preparation of NYC Basal Medium: Combine solution 1, solution 2, and solution 3. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
D-glucose to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Autoclave for 10 min at 10 psi pressure–115°C. Cool to 45°–50°C.
Solution 1: Composition per 600.0mL:
Yeast Dialysate: Composition per 2500.0mL:
deionized water and bring volume to 600.0mL. Mix thoroughly. Melt agar in autoclave for 10 min at 0 psi pressure–100°C. Cool to 45°–50°C.
Baker’s yeast, fresh.........................................908.0g
Preparation of Yeast Dialysate: Add fresh bak-
Agar ..................................................................20.0g
Preparation of Solution 1: Add agar to distilled/
Solution 2: Composition per 40.0mL:
er’s yeast to 2500.0mL of distilled/deionized water. Mix thoroughly. Autoclave for 10 min at 15 psi pressure–121°C. Cool to 25°C. Put into dialysis tubing. Dialyze against 2.0L of distilled/deionized water for 48h at 4°C.
Preparation of Solution 2: Add cornstarch to distilled/deionized water and bring volume to 40.0mL. Mix thoroughly. Warm to 45°–50°C.
Antibiotic VCNT Solution: Composition per 5.0mL:
Solution 3: Composition per 200.0mL:
Colistin.............................................................7.5mg Trimethorprim lactate ......................................3.0mg Vancomycin·HCl..............................................2.0mg Nystatin............................................................12.5U
Cornstarch...........................................................1.0g
Proteose peptone no. 3......................................15.0g NaCl....................................................................5.0g K2HPO4...............................................................4.0g KH2PO4...............................................................1.0g
Preparation of Antibiotic Solution: Add com-
Preparation of Solution 3: Add components to
ponents to distilled/deionized water and bring volume to 5.0mL. Mix thoroughly. Filter sterilize.
distilled/deionized water and bring volume to 200.0mL. Mix thoroughly. Gently heat and bring to boiling. Cool to 45°–50°C.
Preparation of Medium: Have all solutions prepared and at 45°–50°C. Aseptically combine components. Mix thoroughly. Pour into sterile Petri dishes.
Use: For the isolation and cultivation of pathogenic
Glucose Solution: Composition per 10.0mL: D-Glucose ............................................................5.0g
Neisseria species. Used as a transport medium for urogenital and other clinical specimens. For the isolation and presumptive identification of Mycoplasmatales, including large-colony species (Mycoplasma pneumoniae) and T–mycoplasmas from urogenital specimens.
Preparation of Glucose Solution: Add glucose to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Autoclave for 10 min at 10 psi pressure–115°C. Cool to 45°–50°C.
New York City Medium, Modified
Baker’s yeast, fresh.........................................908.0g
Composition per liter: NYC basal medium..................................... 840.0mL α-Gamma horse serum (Flow Labs)........... 120.0mL Yeast dialysate............................................... 25.0mL
Yeast Dialysate: Composition per 2500.0mL: Preparation of Yeast Dialysate: Add fresh Baker’s yeast to 2500.0mL of distilled/deionized water. Mix thoroughly. Autoclave for 10 min at 15 psi pressure–121°C. Cool to 25°C. Put into dialysis tubing.
Nitrate Broth Dialyze against 2.0L of distilled/deionized water for 48h at 4°C.
Antibiotic LCNT Solution: Composition per 5.0mL: Colistin.............................................................7.5mg Lincomycin·HCl ..............................................4.0mg Trimethorprim lactate ......................................3.0mg Nystatin............................................................12.5U
Preparation of Antibiotic LCNT Solution: Add the components to distilled/deionized water and bring volume to 5.0mL. Mix thoroughly. Filter sterilize the solution.
Preparation of Medium: Have all solutions prepared and at 45°–50°C. Aseptically combine components. Mix thoroughly. Pour into sterile Petri dishes.
Use: For the isolation and cultivation of pathogenic Neisseria species. Used as a transport medium for urogenital and other clinical specimens. For the isolation and presumptive identification of Mycoplasmatales, including large-colony species (Mycoplasma pneumoniae) and T–mycoplasmas from urogenital specimens.
NIH Agar Composition per liter: Pancreatic digest of casein................................15.0g Agar ..................................................................15.0g Glucose ...............................................................5.5g Yeast extract........................................................5.0g NaCl ....................................................................2.5g L-Cystine ...........................................................0.05g pH 7.1 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
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L-Cystine .............................................................0.5g
Sodium thioglycolate ..........................................0.5g pH 7.1 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For sterility testing of biological products that are turbid or otherwise cannot be cultivated in fluid thioglycolate broth because of its viscosity.
Nitrate Agar Composition per liter: Agar ..................................................................12.0g Peptone ...............................................................5.0g Beef extract.........................................................3.0g KNO3 ..................................................................1.0g pH 6.8 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes. Autoclave for 15 min at 15 psi pressure–121°C. Allow tubes to cool in a slanted position.
Use: For the differentiation of aerobic and facultative Gram-negative microorganisms based on their ability to reduce nitrate. Test for nitrates with sulfanilic acid and α-naphthylamine reagents. Bacteria that reduce nitrate to nitrite turn the reagents red or pink.
Nitrate Broth (International Streptomyces Project Medium 8) (ISP Medium 8) (ATCC Medium 872)
Use: For the cultivation and maintenance of micro-
Composition per liter:
organisms isolated from sterility testing of biological products. Also used as a solid medium for sterility testing.
Peptone ...............................................................5.0g Beef extract.........................................................3.0g KNO3 ..................................................................1.0g pH 7.0 ± 0.2 at 25°C
NIH Thioglycolate Broth
Source: This medium is available as a premixed
Composition per liter:
powder from BD Diagnostic Systems.
Pancreatic digest of casein................................15.0g Glucose ...............................................................5.5g Yeast extract........................................................5.0g NaCl ....................................................................2.5g
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
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Nitrate Broth
Use: For the differentiation of aerobic and facultative Gram-negative microorganisms based on their ability to reduce nitrate. Test for nitrates with sulfanilic acid and α-naphthylamine reagents. Bacteria that reduce nitrate to nitrite turn the reagents red or pink.
Nitrate Broth Composition per liter: Pancreatic digest of gelatin ...............................20.0g KNO3 ..................................................................2.0g pH 7.2 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the differentiation of aerobic and facultative Gram-negative microorganisms based on their ability to reduce nitrate. Test for nitrates with sulfanilic acid and α-naphthylamine reagents. Bacteria that reduce nitrate to nitrite turn the reagents red or pink.
Nitrate Broth, Campylobacter Composition per liter: Beef heart, solids from infusion......................500.0g Tryptose ............................................................10.0g NaCl ....................................................................5.0g KNO3 ..................................................................2.0g pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.0. Distribute 4.0mL volumes into test tubes that contain inverted Durham tubes. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the differentiation of Campylobacter species based on their ability to reduce nitrate.
Nitrate Reduction Broth Composition per liter: Pancreatic digest of gelatin .................................5.0g Beef extract .........................................................3.0g KNO3 ..................................................................1.0g pH 6.9 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into test tubes that contain an inverted Durham tube. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the differentiation of members of the Pseudomonadaceae based on their ability to reduce
nitrate to nitrite or form N2 gas. Test for nitrates with sulfanilic acid and α-naphthylamine reagents. Bacteria that reduce nitrate to nitrite turn the reagents red or pink.
Nitrate Reduction Broth Composition per liter: Pancreatic digest of casein................................13.0g NaCl....................................................................5.0g Yeast extract........................................................5.0g Heart muscle, solids from infusion.....................2.0g KNO3 or NaNO3 .................................................2.0g pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into test tubes that contain an inverted Durham tube. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the differentiation of a variety of Gramnegative bacteria based on their ability to reduce nitrate to nitrite or form N2 gas. Test for nitrates with sulfanilic acid and α-naphthylamine reagents. Bacteria that reduce nitrate to nitrite turn the reagents red or pink.
Nitrate Reduction Broth Composition per liter: Pancreatic digest of casein................................13.0g NaCl....................................................................5.0g Yeast extract........................................................5.0g Heart muscle, solids from infusion.....................2.0g KNO3 or NaNO3 .................................................2.0g pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Dispense in 3.0mL amounts into screw-capped tubes, add inverted vials, and autoclave at 121°C for 15 min.
Use: For the differentiation of a variety of nonfermenting Gram-negative bacteria based on their ability to reduce nitrate to nitrite or form N2 gas. Test for nitrates with sulfanilic acid and α-naphthylamine reagents. Bacteria that reduce nitrate to nitrite turn the reagents red or pink.
Nitrate Reduction Broth, Clark Composition per liter: Peptone .............................................................20.0g KNO3 or NaNO3 .................................................2.0g
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into test tubes that contain an inverted Durham tube. Autoclave for 15 min at 15 psi pressure–121°C.
NOS Medium, Modified Use: For the differentiation of a variety of Gramnegative bacteria based on their ability to reduce nitrate to nitrite or form N2 gas. Test for nitrates with sulfanilic acid and α-naphthylamine reagents. Bacteria that reduce nitrate to nitrite turn the reagents red or pink.
Nitrate Reduction Broth for Pseudomonas and Related Genera Composition per liter: Peptone................................................................5.0g NaCl ....................................................................5.0g Yeast extract........................................................2.0g Beef extract .........................................................1.0g NaNO3.................................................................0.1g pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into test tubes that contain an inverted Durham tube. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the differentiation of members of the Pseudomonadaceae based on their ability to reduce nitrate to nitrite or form N2 gas. Test for nitrates with sulfanilic acid and α-naphthylamine reagents. Bacteria that reduce nitrate to nitrite turn the reagents red or pink.
NNN Medium (Novy, MacNeal, and Nicole Medium) Composition per liter: Agar ....................................................................7.0g NaCl ....................................................................3.0g Rabbit blood, defibrinated .......................... 150.0mL
Preparation of Medium: Add components, except rabbit blood, to distilled/deionized water and bring volume to 850.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C. Aseptically add sterile rabbit blood. Mix thoroughly. Aseptically distribute into sterile tubes in 5.0mL volumes. Allow tubes to cool in a slanted position at 4°C.
337
flasks. Autoclave for 15 min at 15 psi pressure– 121°C.
Use: For the cultivation of Salmonella species and monkey kidney cells in tissue culture.
Nonnutrient Agar Plates Composition per liter: Agar ..................................................................15.0g Page’s amoeba saline ......................................... 1.0L
Page’s Amoeba Saline: Composition per liter: Na2HPO4 .........................................................0.142g KH2PO4...........................................................0.136g NaCl..................................................................0.12g MgSO4·7H2O ...................................................4.0mg CaCl2·2H2O .....................................................4.0mg
Preparation of Page’s Amoeba Saline: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Preparation of Medium: Add agar to 1.0L of Page’s amoeba saline. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 60°C. Pour into sterile Petri dishes in 20.0mL volumes. Store at 4°C for up to 3 months. Use: For the isolation and cultivation of pathogenic free-living amoebae.
NOS Medium, Modified Composition per 100.67mL: Basal medium ............................................... 94.0mL NaHCO3 solution .......................................... 2.67mL TPP/VFA mixture ........................................... 2.0mL Rabbit serum, heat inactivated........................ 2.0mL pH 7.4 ± 0.2 at 25°C
Basal Medium: Composition per 94.0mL:
Milk, nonfat dry ..............................................100.0g pH 6.8 ± 0.2 at 25°C
Pancreatic digest of casein..................................1.0g Pancreatic digest of gelatin...............................0.48g Yeast extract......................................................0.25g Brain heart, solids from infusion ........................0.2g Peptic digest of animal tissue .............................0.2g D-Glucose ............................................................0.2g NaCl..................................................................0.17g Glucose ...............................................................0.1g L-Cysteine·HCl·H2O............................................0.1g Na2HPO4 .........................................................0.085g Sodium thioglycolate ........................................0.05g L-Asparagine ...................................................0.025g Resazurin (0.1% w/v solution) ....................... 0.1mL
Preparation of Medium: Add 100.0g of nonfat
Preparation of Basal Medium: Add compo-
dry milk to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or
nents to distilled/deionized water and bring volume to 94.0mL. Mix thoroughly. Gently heat and bring to
Use: For the cultivation and maintenance of Leishmania species and Trypanosoma cruzi.
Nonfat Dry Milk, Reconstituted Composition per liter:
338
NOS Spirochete Medium
boiling. Gas under O2-free 85% N2 + 10% CO2 + 5% H2. Stopper and wire flask closed. Autoclave for 20 min at 15 psi pressure–121°C. Cool to 45°–50°C.
NaHCO3 Solution: Composition per 10.0mL: NaHCO3 ............................................................0.75g
Preparation of NaHCO3 Solution: Add the NaHCO3 to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. TPP/VFA Mixture: Composition per 10.9mL: Thiamine pyrophosphate (0.2% solution)....... 1.5mL VFA solution................................................... 1.0mL
Preparation of TPP/VFA Mixture: Add components to distilled/deionized water and bring volume to 10.9mL. Mix thoroughly. Filter sterilize. Store at −20°C.
VFA Solution: Composition per 100.0mL: NaOH (0.1N solution)................................... 98.0mL Isobutyric acid................................................. 0.5mL 2-Methylbutyric acid....................................... 0.5mL Isovaleric acid ................................................. 0.5mL Valeric acid ..................................................... 0.5mL
Preparation of VFA Solution: Add volatile fatty acids to 98.0mL of NaOH solution. Mix thoroughly. Filter sterilize. Store at 4°C.
Preparation of Medium: Open the flask containing 94.0mL of cooled sterile basal medium while flushing with O2-free 85% N2 + 10% CO2 + 5% H2. Aseptically add sterile NaHCO3 solution, sterile TPP/VFA mixture, and filter-sterilized rabbit serum. Mix thoroughly.
Use: For the cultivation and maintenance of Treponema vincentii and other Treponema species.
NOS Spirochete Medium Composition per 1045.0mL: Basal medium .................................................... 1.0L NaHCO3 (10% solution) ............................... 20.0mL Rabbit serum, heat inactivated...................... 20.0mL Thiamine pyrophosphate (0.2% solution)....... 3.0mL VFA solution................................................... 2.0mL pH 7.4 ± 0.2 at 25°C
Basal Medium: Composition per liter: Pancreatic digest of casein................................10.0g Pancreatic digest of gelatin ...............................4.85g Noble agar...........................................................3.0g Yeast extract........................................................2.5g Brain heart, solids from infusion ........................2.0g
Peptic digest of animal tissue .............................2.0g Glucose ...............................................................2.0g NaCl..................................................................1.65g Glucose ...............................................................1.0g L-Cysteine·HCl·H2O............................................1.0g Na2HPO4 ...........................................................0.85g Sodium thioglycolate ..........................................0.5g L-Asparagine .....................................................0.25g
Preparation of Basal Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Gas under O2-free 80% N2 + 10% CO2 + 10% H2. Stopper and wire flask closed. Autoclave for 20 min at 15 psi pressure–121°C. Cool to 45°–50°C.
VFA Solution: Composition per 100.0mL: KOH (0.1N solution) .................................... 98.0mL Isobutyric acid ................................................ 0.5mL 2-Methylbutyric acid ...................................... 0.5mL Isovaleric acid................................................. 0.5mL Valeric acid ..................................................... 0.5mL
Preparation of VFA Solution: Add volatile fatty acids to 98.0mL of KOH solution. Mix thoroughly. Filter sterilize. Store at 4°C.
Preparation of Medium: Combine 20.0mL of NaHCO3 solution, 20.0mL of rabbit serum, 3.0mL of thiamine pyrophosphate solution, and 2.0mL of VFA solution. Mix thoroughly. Filter sterilize. Open the flask containing 1.0L of cooled, sterile basal medium while flushing with O2-free 85% N2 + 10% CO2 + 5% H2. Aseptically add the filter-sterilized mixture. Mix thoroughly. Aseptically and anaerobically distribute into sterile tubes or flasks.
Use: For the cultivation and maintenance of Treponema denticola and Treponema socranskii.
Novobiocin Agar Composition per liter: Agar ..................................................................15.0g Peptone ...............................................................5.0g NaCl....................................................................5.0g Yeast extract........................................................2.0g Beef extract.........................................................1.0g Novobiocin solution...................................... 10.0mL
Novobiocin Solution: Composition per 10.0mL: Novobiocin ....................................................10.0mg
Preparation of Novobiocin Solution: Add novobiocin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except novobiocin solution, to distilled/deionized water
Nutrient Agar with Dihydrostreptomycin and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Aseptically add 10.0mL of sterile novobiocin solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation of Staphylococcus aureus.
Nutrient Agar (LMG Medium 160) Composition per liter: Agar ....................................................................3.0g Lab-Lemco beef extract ......................................1.0g Peptone................................................................1.0g NaCl ....................................................................0.5g pH 7.3 ± 0.2 at 25°C
339
Mix thoroughly. Gently heat while stirring and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation of a wide variety of bacteria.
Nutrient Agar with Formate, Fumarate, and Horse Blood (LMG Medium 250) Composition per liter:
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Agar ..................................................................15.0g Peptone .............................................................. 5.0g NaCl....................................................................5.0g Fumaric acid .......................................................3.0g Sodium formate ..................................................2.0g Yeast extract........................................................2.0g Lab-Lemco beef extract......................................1.0g Horse blood, sterile defibrinated................... 50.0mL pH 7.2 ± 0.2 at 25°C
Use: For the cultivation of heterotrophic bacteria.
Preparation of Medium: Add components, ex-
Preparation of Medium: Add components to
Nutrient Agar Composition per liter: Agar ..................................................................15.0g Peptone................................................................5.0g NaCl ....................................................................5.0g Yeast extract........................................................2.0g Beef extract .........................................................1.0g pH 7.4 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath.
cept horse blood, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Adjust pH to 7.2. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°C. Aseptically add 50.0mL sterile defibrinated horse blood. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation and maintenance of Campylobacter rectus and Campylobacter gracilis.
Nutrient Agar No. 2
Preparation of Medium: Add components to
Composition per liter:
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Agar ..................................................................20.0g Meat extract ......................................................10.0g Peptone .............................................................10.0g NaCl....................................................................5.0g pH 7.0 ± 0.2 at 25°C
Use: For the cultivation and maintenance of a wide
Preparation of Medium: Add components to
variety of microorganisms.
Nutrient Agar (ATCC Medium 3) Composition per liter: Agar ..................................................................15.0g Pancreatic digest of gelatin .................................5.0g Beef extract .........................................................3.0g pH 6.8 ± 0.2 at 25°C
Source: This medium is available as a premixed
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of a wide variety of bacteria.
Nutrient Agar with Dihydrostreptomycin
powder from BD Diagnostic Systems.
Composition per liter:
Preparation of Medium: Add components to
Agar ..................................................................15.0g Pancreatic digest of gelatin.................................5.0g
distilled/deionized water and bring volume to 1.0L.
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Nutrient Agar with Horse Serum
Beef extract .........................................................3.0g Dihydrostreptomycin solution ...................... 10.0mL pH 6.8 ± 0.2 at 25°C
Source: Nutrient agar is available as a premixed
Source: Nutrient agar is available as a premixed
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
powder from BD Diagnostic Systems.
Dihydrostreptomycin Solution: Composition per 10.0mL: Dihydrostreptomycin ......................................0.625g
Preparation of Dihydrostreptomycin Solution: Add dihydrostreptomycin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except dihydrostreptomycin solution, to distilled/ deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile dihydrostreptomycin solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation and maintenance of Escherichia coli, Micrococcus luteus, Shigella species, and Vibrio cholerae.
Nutrient Agar with Horse Serum (LMG Medium 38) Composition per liter: Agar ..................................................................15.0g Peptone............................................................... 5.0g NaCl ....................................................................5.0g Yeast extract........................................................2.0g Lab-Lemco beef extract ......................................1.0g Horse serum ................................................ 100.0mL pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components, except horse serum, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool medium to 45-50°C. Aseptically add 100.0mL of sterile horse serum. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation of fastidious bacteria.
Nutrient Agar with 0.5% NaCl Composition per liter: Agar ..................................................................15.0g NaCl ....................................................................5.0g Pancreatic digest of gelatin .................................5.0g Beef extract .........................................................3.0g pH 6.8 ± 0.2 at 25°C
powder from BD Diagnostic Systems.
Preparation of Medium: Add components to
Use: For the cultivation and maintenance of Pseudomonas aeruginosa, Shigella dysenteriae, Shigella flexneri, Vibrio species, and Yersinia species.
Nutrient Agar with 2% NaCl Composition per liter: NaCl..................................................................20.0g Agar ..................................................................15.0g Pancreatic digest of gelatin.................................5.0g Beef extract.........................................................3.0g pH 6.8 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of Vibrio parahaemolyticus and Vibrio vulnificus.
Nutrient Agar with Yeast Extract Composition per liter: Yeast extract......................................................20.0g Agar ..................................................................15.0g Pancreatic digest of gelatin.................................5.0g Beef extract.........................................................3.0g pH 6.8 ± 0.2 at 25°C
Source: Nutrient agar is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of Bacillus anthracis and Comamonas testosteroni.
Nutrient Broth Composition per liter: Peptone ...............................................................5.0g NaCl....................................................................5.0g
N-Z Amine A Medium with Soluble Starch and Glucose Yeast extract........................................................2.0g Beef extract .........................................................1.0g pH 7.4 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath.
341
Use: For the cultivation of a variety of fastidious and nonfastidious microorganisms.
Nutrient Gelatin Composition per liter:
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Gelatin.............................................................120.0g Pancreatic digest of gelatin.................................5.0g Beef extract.........................................................3.0g pH 6.8 ± 0.2 at 25°C
Use: For the cultivation of a wide variety of nonfas-
Source: This medium is available as a premixed
Preparation of Medium: Add components to
tidious microorganisms.
Nutrient Broth Composition per liter: Pancreatic digest of gelatin .................................5.0g Beef extract .........................................................3.0g pH 6.9 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of a wide variety of nonfastidious microorganisms.
Nutrient Broth No. 2 Composition per liter: Beef extract .......................................................10.0g Peptone..............................................................10.0g NaCl ....................................................................5.0g pH 7.5 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of a variety of fastidious and nonfastidious microorganisms.
Nutrient Broth, Standard II Composition per liter: Special peptone ...................................................8.6g NaCl ....................................................................6.4g pH 7.5 ± 0.1 at 37°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
powder from BD Diagnostic Systems and Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring to 50°C. Distribute into tubes. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation and differentiation of bacteria based on their ability to liquefy gelatin.
N-Z Amine A™ Glycerol Agar Composition per liter: Agar ..................................................................15.0g N-Z-Amine A......................................................5.0g Beef extract.........................................................1.0g Glycerol ........................................................ 70.0mL pH 6.5–7.0 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the isolation and cultivation of Actinomadura species, Actinopolyspora species, Excellospora species, and Microspora species.
N-Z Amine A Medium with Soluble Starch and Glucose Composition per liter: Soluble starch....................................................20.0g Agar ..................................................................15.0g Glucose .............................................................10.0g Yeast extract........................................................5.0g N-Z-Amine A......................................................5.0g CaCO3 .................................................................1.0g
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
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NZY Agar
Use: For the cultivation and maintenance of Actinomadura species.
NZY Agar Composition per liter: Agar ..................................................................20.0g N-Z- Amine A...................................................10.0g NaCl ....................................................................5.0g Yeast extract........................................................5.0g MgCl2·6H2O .......................................................2.0g
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes. Autoclave for 15 min at 15 psi pressure–121°C. Allow tubes to cool in a slanted position.
Use: For the cultivation and maintenance of a variety of microorganisms.
Salicin ...............................................................10.0g Inositol ..............................................................10.0g Peptone .............................................................10.0g Adonitol ..............................................................8.0g NaCl....................................................................5.0g Tryptone..............................................................5.0g Proteose peptone.................................................3.0g Bile salts no. 3...................................................1.25g Indoxyl-β-D-galactopyranoside ........................0.12g 5-Bromo-4-chloro-3-indoxylβ-D-galactopyranoside................................0.12g Phenol Red..........................................................0.1g Isopropyl-β-D-thiogalactopyranoside .................0.1g Novobiocin solution........................................ 1.0mL Tellurite solution ............................................. 1.0mL pH 6.8 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BIOSYNTH International, Inc.
NZY Agar Composition per liter: Agar ..................................................................11.0g N-Z-Amine A....................................................10.0g NaCl ....................................................................5.0g Yeast extract........................................................5.0g MgCl2·6H2O .......................................................2.0g
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes.
Use: For the cultivation and enumeration of a variety of microorganisms.
NZY Broth Composition per liter: N-Z-Amine A....................................................10.0g NaCl ....................................................................5.0g Yeast extract........................................................5.0g MgCl2·6H2O .......................................................2.0g
Preparation of Medium: Add components to
Novobiocin Solution: Composition per 10.0mL: Novobiocin .........................................................0.1g
Preparation of Novobiocin Solution: Add novobiocin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Tellurite Solution: Composition per 10.0mL: K2TeO3 ..............................................................0.01g
Preparation of Tellurite Solution: Add K2TeO3
to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Caution: Potassium tellurite is toxic. Preparation of Medium: Add components, except novobiocin solution and tellurite solution, to distilled/deionized water and bring volume to 998.0mL. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 50°C. Aseptially add 1.0mL sterile novobiocin solution and 1.0 sterile tellurite solution. Mix thoroughly. Pour into sterile Petri dishes.
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the detection of Escherichia coli O157:H7. E.coli O157:H7 grow with blue-black colonies and E.coli non-O157 with green-yellow colonies.
Use: For the cultivation of a variety of microorgan-
O157:H7 ID Agar
isms.
Composition per liter:
O157:H7(+) Plating Medium
Proprietary
Composition per liter:
Source: This medium is available from bioMérieux.
Agar ..................................................................15.0g Sorbitol..............................................................12.0g
Use: A new chromogenic medium for the detection of Escherichia coli O157:H7.
Önöz Salmonella Agar
Oatmeal Agar Composition per 750.0mL: Oatmeal, instant for babies ...............................40.0g Agar ....................................................................5.0g
Preparation of Medium: Add agar to distilled/ deionized water and bring volume to 500.0mL. Mix thoroughly. Gently heat and bring to boiling. Add instant oatmeal for babies to distilled/deionized water and bring volume to 250.0mL. Mix thoroughly. Add the oatmeal solution to the melted agar solution. Mix thoroughly. Autoclave for 15 min at 15 psi pressure– 121°C. Pour into sterile Petri dishes or aseptically distribute into sterile tubes.
Use: For the cultivation of fungi.
Oatmeal Agar (ATCC 551) Composition per liter: Oatmeal.............................................................60.0g Agar ..................................................................12.5g pH 6.0 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For cultivation of fungi and actinomycetes, particularly for macrospore formation.
Oatmeal Agar (OA) Composition per liter: Agar ..................................................................12.0g Oatmeal, rolled oats ..........................................10.0g Glycerin .......................................................... 5.0mL Lactic acid....................................................... 0.2mL
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation of many filamentous fungi.
Ogawa TB Medium Composition per 300.0mL: KH2PO4 ...............................................................1.0g Homogenized whole egg ............................ 200.0mL
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Glycerol .......................................................... 6.0mL Malachite Green (2% solution)....................... 6.0mL pH 6.5 ± 0.2 at 25°C
Homogenized Whole Egg: Composition per liter: Whole eggs ......................................................18–24
Preparation of Homogenized Whole Egg: Use fresh eggs, less than 1 week old. Scrub the shells with soap. Let stand in a soap solution for 30 min. Rinse in running water. Soak eggs in 70% ethanol for 15 min. Break the eggs into a sterile container. Homogenize by shaking. Filter through four layers of sterile cheesecloth into a sterile graduated cylinder. Measure out 1.0L.
Preparation of Medium: Add components, except homogenized whole egg, to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 200.0mL of sterile homogenized whole egg. Mix thoroughly. Aseptically distribute into sterile screw-capped tubes in 7.0mL volumes. Inspissate at 85°–90°C (moist heat) for 60 min.
Use: For the isolation and cultivation of Mycobacterium species, except for Mycobacterium leprae.
Oleic Albumin Complex Composition per liter: Bovine albumin fraction V ...............................50.0g NaCl....................................................................8.5g Oleic acid ........................................................ 0.6mL
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
Use: For use in media employed for the cultivation of mycobacteria.
Önöz Salmonella Agar Composition per liter: Agar ..................................................................15.0g Sucrose..............................................................13.0g Lactose.............................................................. 11.5g Trisodium citrate–5,5–hydrate............................9.3g Meat peptone ......................................................6.8g Beef extract.........................................................6.0g L–Phenylalanine ..................................................5.0g Na2S2O3·5H2O ..................................................4.25g Bile salt mixture..............................................3.825g Yeast extract........................................................3.0g Na2HPO4·2H2O...................................................1.0g Ferric citrate........................................................0.5g Metachrome Yellow..........................................0.47g
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ONPG Broth
MgSO4·7H2O ......................................................0.4g Aniline Blue......................................................0.25g Neutral Red .....................................................0.022g Brilliant Green ............................................0.00166g pH 7.1 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the isolation and cultivation of Salmonella from feces.
ONPG Broth Composition per liter: Peptone water.............................................. 750.0mL ONPG solution............................................ 250.0mL pH 7.2–7.4 at 25°C
ONPG Solution: Composition per 250.0mL: ONPG (o-Nitrophenyl-βD-galactopyranoside) ....................................1.5g Sodium phosphate buffer (0.01M, pH 7.5) ......................... 250.0mL
Preparation of ONPG Solution: Add ONPG to 250.0mL of sodium phosphate buffer. Mix thoroughly. Filter sterilize.
Peptone Water: Composition per 750.0mL: Peptone................................................................7.5g NaCl ..................................................................3.75g
Preparation of Peptone Water: Add components to distilled/deionized water and bring volume to 750.0mL. Mix thoroughly. Gently heat and bring to boiling. Adjust pH to 8.0–8.4. Continue boiling for 10 min. Filter through Whatman no. 1 filter paper. Readjust pH of filtrate to 7.2–7.4. Autoclave for 20 min at 10 psi pressure–115°C. Cool to 25°C.
Preparation of Medium: Aseptically combine the sterile ONPG solution with the cooled, sterile peptone water. Mix thoroughly. Aseptically distribute into tubes in 2.5–3.0mL volumes. Store at 4°C for up to 1 month.
Use: For the differentiation of a variety of Gram-
negative bacteria based on production of β-galactosidase. For the differentiation of lactose-delayed bacteria from lactose-negative bacteria. For the differentiation of Pseudomonas cepacia (positive) and Pseudomonas maltophila (positive) from other Pseudomonas species (negative). Bacteria that produce β-galactosidase turn the medium yellow.
OR Indicator Agar (Oxidation-Reduction Indicator Agar) Composition per liter: Agar ..................................................................15.0g Sodium glycerol phosphate...............................10.0g Sodium thioglycolate ..........................................1.7g CaCl2·2H2O ........................................................0.1g Methylene Blue................................................6.0mg
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For use as an indicator of oxygen-free conditions in anaerobic culture chambers.
Oral Fusobacterium Medium Composition per liter: Agar ..................................................................15.0g Proteose peptone...............................................10.0g Na2HPO4 .............................................................5.0g Glucose ...............................................................5.0g Beef extract.........................................................3.0g Soluble starch......................................................2.0g NaNO3 ................................................................1.0g Yeast extract........................................................1.0g L-Cysteine·HCl·H2O ...........................................0.5g Ethyl Violet solution ..................................... 10.0mL Bacitracin solution ........................................ 10.0mL pH 7.6 ± 0.2 at 25°C
Ethyl Violet Solution: Composition per 10.0mL: Ethyl Violet.......................................................0.04g
Preparation of Ethyl Violet Solution: Add Ethyl Violet to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Bacitracin Solution: Composition per 10.0mL: Bacitracin.........................................................1.0mg
Preparation of Bacitracin Solution: Add bacitracin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except Ethyl Violet solution and bacitracin solution, to distilled/deionized water and bring volume to 980.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C. Aseptically add sterile Ethyl Violet solution and bacitracin solution. Mix
Ornithine Broth with NaCl thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the selective isolation and cultivation of oral Fusobacterium species, especially Fusobacterium nucleatum.
Oral Treponema Medium Composition per 1250.0mL: Veal heart, fresh ground ...................................1.0Kg Thiopeptone ......................................................20.0g NaCl ..................................................................10.0g Ionagar no. 2 .......................................................2.0g Glutathione (1% solution)........................... 100.0mL Rabbit serum or ascitic fluid....................... 100.0mL Eggs, whole fresh.....................................................2 pH 6.8–7.0 at 25°C
Preparation of Medium: Add agar to 50.0mL of distilled/deionized water. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C. In a separate flask, add finely ground veal heart to 1.0L of distilled/deionized water. Add remaining components, except glutathione, rabbit serum, and agar. Gently heat and bring to 70°C. Adjust pH to 7.4. Gently heat and bring to 100°C. Continue heating at 100°C for 2h. Skim off fat. Filter through glass wool. Adjust pH to 7.6. Gently heat and bring to 100°C. Maintain at 100°C for 30 min. Store at 4°C for 18h. Sterilize in an Arnold sterilizer for 30 min at 100°C on two consecutive days. Cool to 45°–50°C. Aseptically add rabbit serum, glutathione solution, and sterile cooled agar solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the isolation and cultivation of Treponema denticola and Treponema oralis.
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Preparation of Medium: Add components, except organic acid solution, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile organic acid solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation and differentiation of members of the Enterobacteriaceae based on their ability to utilize different organic acids as carbon source. Bacteria that utilize tartrate, citrate, or mucate turn the medium yellow.
Ornithine Broth Composition per liter: L-Ornithine..........................................................5.0g
Peptone or gelysate .............................................5.0g Yeast extract........................................................3.0g Glucose ...............................................................1.0g Bromcresol Purple ............................................0.02g pH 6.5 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH so that is will be 6.5 ± 0.2 after sterilization. Distribute into 16 × 150mm screw-capped tubes in 5.0mL volumes. Autoclave medium with loosely capped tubes for 10 min at 15 psi pressure– 121°C. Screw the caps on tightly for storage and after inoculation.
Use: For the cultivation and differentiation of bacteria based on their ability to decarboxylate the amino acid ornithine. Bacteria that decarboxylate ornithine turn the medium turbid purple.
Ornithine Broth with NaCl Composition per liter: L-Ornithine..........................................................5.0g
Organic Acid Medium KP (Organic Acid Medium, Kauffmann and Petersen) Composition per liter: Gelatin...............................................................10.0g Bromthymol Blue ...........................................0.024g Organic acid solution .................................. 100.0mL pH 7.4 ± 0.2 at 25°C
Organic Acid Solution: Composition per 100.0mL: Organic acid ......................................................10.0g
Preparation of Organic Acid Solution: Add organic acid to distilled/deionized water and bring volume to 100.0mL. Sodium potassium D-tartrate, sodium citrate, or mucic acid may be used. Mix thoroughly.
Peptone or gelysate .............................................5.0g Yeast extract........................................................3.0g Glucose ...............................................................1.0g Bromcresol Purple ............................................0.02g pH 6.5 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH so that is will be 6.5 ± 0.2 after sterilization. Distribute into 16 × 150mm screw-capped tubes in 5.0mL volumes. Autoclave medium with loosely capped tubes for 10 min at 15 psi pressure– 121°C. Screw the caps on tightly for storage and after inoculation.
Use: For the cultivation and differentiation of Vibrio spp. based on their ability to decarboxylate the amino acid ornithine. Bacteria that decarboxylate ornithine turn the medium turbid purple.
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Oxford Agar
Oxford Agar (Listeria Selective Agar, Oxford) Composition per liter: Special peptone .................................................23.0g LiCl ...................................................................15.0g Agar ..................................................................10.0g NaCl ....................................................................5.0g Cornstarch...........................................................1.0g Esculin ................................................................1.0g Ferric ammonium citrate.....................................0.5g Antibiotic inhibitor ....................................... 10.0mL pH 7.0 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath. Antibiotic Inhibitor: Composition per 10.0mL: Cycloheximide ....................................................0.4g Colistin sulfate ..................................................0.02g Fosfomycin .......................................................0.01g Acriflavine .......................................................5.0mg Cefotetan ..........................................................2.0mg Ethanol (50% solution) ................................. 10.0mL
Antibiotic Inhibitor: Composition per 10.0mL: Moxalactam ....................................................0.015g Colistin sulfate ..................................................0.01g
Preparation of Antibiotic Inhibitor: Add components to distilled /deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except antibiotic inhibitor, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 10 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 10.0mL of sterile antibiotic inhibitor. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation and cultivation of Listeria monocytogenes from specimens containing a mixed bacterial flora.
Oxidation-Fermentation Medium (OF Medium)
Preparation of Antibiotic Inhibitor: Add anti-
Composition per liter:
biotics to 10.0mL of ethanol. Mix thoroughly. Filter sterilize.
NaCl....................................................................5.0g Agar ....................................................................2.5g Pancreatic digest of casein..................................2.0g K2HPO4...............................................................0.3g Bromthymol Blue .............................................0.03g Carbohydrate solution................................. 100.0mL pH 6.8 ± 0.1 at 25°C
Preparation of Medium: Add components, except antibiotic inhibitor, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 10.0mL of sterile antibiotic inhibitor. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation and cultivation of Listeria monocytogenes from specimens containing a mixed bacterial flora.
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Carbohydrate Solution: Composition per 100.0mL: Carbohydrate.....................................................10.0g
Oxford Agar, Modified (Listeria Selective Agar, Modified Oxford) (MOX Agar) Composition per liter: Special peptone .................................................23.0g LiCl ...................................................................15.0g Agar ..................................................................12.0g NaCl ....................................................................5.0g Cornstarch...........................................................1.0g Esculin ................................................................1.0g Ferric ammonium citrate.....................................0.5g Antibiotic inhibitor ....................................... 10.0mL pH 7.0 ± 0.2 at 25°C
Preparation of Carbohydrate Solution: Add carbohydrate to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except carbohydrate solution, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 100.0mL of sterile carbohydrate solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For differentiating Gram-negative bacteria based upon determining the oxidative and fermentative metabolism of carbohydrates.
Oxidative-Fermentative Medium
Oxidation-Fermentation Medium, Hugh-Leifson’s (Hugh-Leifson’s Oxidation Fermentation Medium) Composition per liter: NaCl ....................................................................5.0g Agar ....................................................................3.0g Peptone................................................................2.0g K2HPO4 ...............................................................0.3g Carbohydrate solution................................. 100.0mL Bromthymol Blue solution (0.2% )............... 15.0mL pH 7.1 ± 0.2 at 25°C
Carbohydrate Solution: Composition per 100.0mL: Carbohydrate.....................................................10.0g
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Preparation of Carbohydrate Solution: Add carbohydrate to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except carbohydrate solution, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 100.0mL of sterile carbohydrate solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For differentiating bacteria based upon determining the oxidative and fermentative metabolism of carbohydrates. Bacteria that ferment the carbohydrate turn the medium yellow.
Preparation of Carbohydrate Solution: Add carbohydrate to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except carbohydrate solution, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 100.0mL of sterile carbohydrate solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For differentiating Gram-negative bacteria, such as Vibrio species, based upon determining the oxidative and fermentative metabolism of carbohydrates. Bacteria that ferment the carbohydrate turn the medium yellow.
Oxidation-Fermentation Medium, King’s (King’s OF Medium) Composition per liter:
Oxidative-Fermentative Medium (OF Medium) Composition per liter: NaCl....................................................................5.0g Agar ....................................................................2.0g Pancreatic digest of casein..................................2.0g K2HPO4...............................................................0.3g Bromthymol Blue .............................................0.08g Carbohydrate solution................................. 100.0mL pH 6.8 ± 0.1 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems and Oxoid Unipath.
Carbohydrate Solution: Composition per 100.0mL: Carbohydrate.....................................................10.0g
Base solution............................................... 900.0mL Carbohydrate solution................................. 100.0mL pH to 7.3 ± 0.2
Preparation of Carbohydrate Solution: Add
Base Solution: Composition per liter:
Preparation of Medium: Add components, ex-
Agar ....................................................................3.0g Pancreatic digest of casein..................................2.0g Carbohydrate solution................................. 100.0mL Phenol Red (1.5% solution) ............................ 2.0mL
Preparation of Base Solution: Add carbohydrate to distilled/deionized water and bring volume to 1.0L. Mix thoroughly.
Carbohydrate Solution: Composition per 100.0mL: Carbohydrate.....................................................10.0g
carbohydrate to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize. cept carbohydrate solution, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 100.0mL of sterile carbohydrate solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For differentiating bacteria based upon determining the oxidative and fermentative metabolism of carbohydrates. Bacteria that ferment the carbohydrate turn the medium yellow.
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Oxidative-Fermentative Glucose Medium, Semisolid
Oxidative-Fermentative Glucose Medium, Semisolid (OF Glucose Medium, Semisolid) Composition per liter: Glucose .............................................................10.0g NaCl ....................................................................5.0g Agar ....................................................................2.0g Pancreatic digest of casein..................................2.0g K2HPO4 ...............................................................0.3g Bromthymol Blue dye.......................................0.08g pH 6.8 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For differentiating Gram-negative bacteria based upon determining the oxidative and fermentative metabolism of glucose. Bacteria that ferment glucose turn the medium yellow.
Oxidative-Fermentative Glucose Medium, Semisolid, with NaCl (OF Glucose Medium, Semisolid with NaCl) Composition per liter: NaCl ..................................................................20.0g Glucose .............................................................10.0g Agar ....................................................................2.0g Pancreatic digest of casein..................................2.0g K2HPO4 ...............................................................0.3g Bromthymol Blue dye.......................................0.08g pH 6.8 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For differentiating Vibrio species based upon determining the oxidative and fermentative metabolism of glucose. Bacteria that ferment glucose turn the medium yellow.
Oxidative-Fermentative Test Medium (OF Test Medium) Composition per liter: NaCl ....................................................................5.0g Agar ....................................................................3.0g Peptone................................................................2.0g K2HPO4 ...............................................................0.3g
Bromthymol Blue .............................................0.03g Carbohydrate solution................................. 100.0mL
Carbohydrate Solution: Composition per 100.0mL: Carbohydrate.....................................................10.0g
Preparation of Carbohydrate Solution: Add carbohydrate to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except carbohydrate solution, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes in 3.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 0.3mL of sterile carbohydrate solution to each tube. Mix thoroughly.
Use: For the cultivation and differentiation of a variety of microorganisms based on their ability to ferment a specific carbohydrate. Bacteria that ferment the specific carbohydrate turn the medium yellow.
P Agar Composition per liter: Agar ..................................................................15.0g Peptone .............................................................10.0g NaCl....................................................................5.0g Yeast extract........................................................5.0g Glucose ...............................................................1.0g pH 7.5 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation of Staphylococcus species.
Pagano Levin Agar Composition per liter: Glucose .............................................................40.0g Agar ..................................................................15.0g Peptone .............................................................10.0g Yeast extract........................................................1.0g Neomycin............................................................0.5g 2,3,5-Triphenyltetrazolium chloride ...................0.1g pH 6.0 ± 0.1 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components, except neomycin and 2,3,5-triphenyltetrazolium chloride, to distilled/deionized water and bring volume to
PALCAM Agar 1.0L. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add neomycin and 2,3,5-triphenyltetrazolium chloride. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes. Allow tubes to cool in a slanted position.
Use: For the isolation, cultivation, and differentiation of Candida species. Candida albicans appears as smooth, shiny, cream-light pink colonies.
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tubes. Inspissate tubes in a slanted position at 80°– 90°C (moist heat) for 30 min.
Use: For the isolation and cultivation of Corynebacterium spp.
PALCAM Agar (Polymyxin Acriflavine LiCl Ceftazidime Esculin Mannitol Agar) Composition per liter:
Pai Medium Composition per liter: Homogenized whole egg ............................ 666.0mL NaCl (0.85% solution) ................................ 334.0mL pH 6.75 ± 0.2 at 25°C
Homogenized Whole Egg: Composition per liter: Whole eggs ...................................................... 18-24
Preparation of Homogenized Whole Egg: Use fresh eggs, less than 1 week old. Scrub the shells with soap. Let stand in a soap solution for 30 min. Rinse in running water. Soak eggs in 70% ethanol for 15 min. Break the eggs into a sterile container. Homogenize by shaking. Filter through four layers of sterile cheesecloth into a sterile graduated cylinder. Measure out 1.0L. Preparation of Medium: Combine components. Mix thoroughly. Aseptically distribute into sterile tubes. Inspissate tubes in a slanted position at 80°– 90°C (moist heat) for 30 min.
Use: For the maintenance of stock cultures of Salmonella typhi and other Salmonella species.
Pai Medium Composition per 1620.0mL: Glucose ...............................................................5.0g Homogenized whole egg ................................... 1.0L Glycerol ...................................................... 120.0mL pH 6.75 ± 0.2 at 25°C
Homogenized Whole Egg: Composition per liter:
Peptone .............................................................23.0g LiCl ...................................................................15.0g Agar ..................................................................10.0g Mannitol............................................................10.0g NaCl....................................................................5.0g Yeast extract........................................................3.0g Starch ..................................................................1.0g Esculin ................................................................0.8g Ferric ammonium citrate.....................................0.5g Glucose ...............................................................0.5g Phenol Red........................................................0.08g PALCAM selective supplement.................... 10.0mL pH 7.2 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath.
PALCAM Selective Supplement: Composition per 10.0mL: Ceftazidime....................................................20.0mg Polymyxin B ..................................................10.0mg Acriflavine·HCl ...............................................5.0mg
Preparation of PALCAM Selective Supplement: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Egg Yolk Emulsion: Composition: Chicken egg yolks.................................................. 11 Whole chicken egg ..................................................1
Preparation of Egg Yolk Emulsion: Soak eggs
Whole eggs ......................................................18–24
with 1:100 dilution of saturated mercuric chloride solution for 1 min. Crack eggs and separate yolks from whites. Mix egg yolks with 1 chicken egg.
Preparation of Homogenized Whole Egg:
Preparation of Medium: Add components, ex-
Use fresh eggs, less than 1 week old. Scrub the shells with soap. Let stand in a soap solution for 30 min. Rinse in running water. Soak eggs in 70% ethanol for 15 min. Break the eggs into a sterile container. Homogenize by shaking. Filter through four layers of sterile cheesecloth into a sterile graduated cylinder. Measure out 1.0L.
Preparation of Medium: Combine components. Mix thoroughly. Aseptically distribute into sterile
cept PALCAM selective supplement, to distilled/ deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile PALCAM selective supplement. Mix thoroughly. The addition of 25.0mL of egg yolk emulsion may aid in the recovery of damaged Listeria. Pour into sterile Petri dishes or distribute into sterile tubes.
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Pasteurella haemolytica Selective Medium
Use: For the selective isolation, cultivation, and differentiation of Listeria monocytogenes and other Listeria species.
Peptic digest of animal tissue ...........................10.0g NaCl....................................................................5.0g Glucose ...............................................................1.0g Peptic digest of blood ................................... 50.0mL
Pasteurella haemolytica Selective Medium
Preparation of Tryptose Agar with Peptic Digest of Blood: Add components to distilled/
Composition per 1010.0mL: Tryptose agar with peptic digest of blood.......... 1.0L Antibiotic solution ........................................ 10.0mL pH 7.2 ± 0.2 at 25°C
Tryptose Agar With Peptic Digest of Blood: Composition per liter: Agar ..................................................................15.0g Pancreatic digest of casein................................10.0g Peptic digest of animal tissue............................10.0g NaCl ....................................................................5.0g Glucose ...............................................................1.0g Peptic digest of blood ................................... 50.0mL
Preparation of Tryptose Agar With Peptic Digest of Blood: Add components to distilled/ deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add peptic digest of blood. Mix thoroughly.
Antibiotic Solution: Composition per 10.0mL: Actidione (cycloheximide) .................................0.1g Novobiocin.......................................................2.0mg Neomycin.........................................................1.5mg
Preparation of Antibiotic Solution: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: To 1.0L of cooled, sterile tryptose agar with peptic digest of blood, aseptically add 10.0mL of sterile antibiotic solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the selective cultivation of Pasteurella haemolytica.
Pasteurella multocida Selective Medium Composition per 1020.0mL: Tryptose agar with peptic digest of blood .. 1.0L Antibiotic solution ........................................ 10.0mL K2TeO3 solution ............................................ 10.0mL pH 7.2 ± 0.2 at 25°C
Tryptose Agar With Peptic Digest of Blood: Composition per liter: Agar ..................................................................15.0g Pancreatic digest of casein................................10.0g
deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add peptic digest of blood. Mix thoroughly.
Antibiotic Solution: Composition per 10.0mL: Actidione (cycloheximide) .................................0.1g Novobiocin .......................................................0.01g Erythrocin ........................................................5.0mg
Preparation of Antibiotic Solution: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
K2TeO3 Solution: Composition per 10.0mL: K2TeO3 .............................................................5.0mg
Preparation of K2TeO3 Solution: Add K2TeO3
to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Caution: Potassium tellurite is toxic. Preparation of Medium: To 1.0L of cooled, sterile tryptose agar with peptic digest of blood, aseptically add 10.0mL of sterile antibiotic solution and 10.0mL of sterile K2TeO3 solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the selective cultivation of Pasteurella multocida.
PDM-114 Medium Composition per liter: Base solution............................................... 770.0mL Bovine serum, heat inactivated................... 100.0mL Solution A..................................................... 50.0mL Solution B ..................................................... 50.0mL Special 107 vitamin mix ............................... 30.0mL pH 6.8 ± 0.2 at 25°C
Base Solution: Composition per 770.0mL: Pancreatic digest of casein................................20.0g NaCl................................................................... 2.0g L-Cysteine·HCl ...................................................1.0g Ascorbic acid ..................................................... 0.2g Ammonium chloride.........................................0.16g Adenine..........................................................73.0mg Guanosine ......................................................59.0mg
Peptone Iron Agar Adenosine 5´-monophosphate .......................52.0mg Uracil .............................................................37.0mg Cytosine ........................................................ 30.0mg Ferric ammonium citrate................................22.8mg Adenosine 5´-diphosphate .............................16.6mg Adenosine 5´-triphosphate...............................7.6mg
Preparation of Base Solution: Add components to distilled/deionized water and bring volume to 770.0mL. Mix thoroughly. Adjust pH to 6.8 with NaOH. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to room temperature.
Solution A: Composition per 50.0.0mL: Glucose .............................................................10.0g
Preparation of Solution A: Add glucose to distilled/deionized water and bring volume to 50.0mL. Mix thoroughly. Filter sterilize.
Solution B: Composition per 50.0.0mL:
351
Solution 4 Vitamins: Composition per liter: Vitamin B12 ....................................................10.0mg Calcium D-(+)-pantothenate ............................2.3mg Choline chloride.............................................1.25mg Riboflavin ........................................................0.7mg Vitamin A, crystallized alcohol .....................0.25mg Calciferol (vitamin D2) ..................................0.25mg i-Inositol.......................................................0.125mg p-Aminobenzoic acid...................................0.125mg Niacin.........................................................0.0625mg Niacinamide...............................................0.0625mg Pyridoxal·HCl ............................................0.0625mg Pyridoxine·HCl ..........................................0.0625mg α-Tocopherol phosphate, disodium salt ......0.025mg Biotin ...........................................................0.025mg Folic acid .....................................................0.025mg Menadione (vitamin K3) ..............................0.025mg Thiamine·HCl ..............................................0.025mg
Preparation of Solution 4 Vitamins: Add com-
K2HPO4 ...............................................................1.0g KH2PO4 ...............................................................0.6g
ponents to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
Preparation of Solution B: Add components to
Preparation of Special 107 Vitamin Mix:
distilled/deionized water and bring volume to 50.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to room temperature.
Special 107 Vitamin Mix: Composition per 120.0.0mL: Solution 4 vitamins ..................................... 100.0mL Solution 2........................................................ 1.2mL Solution 1........................................................ 0.4mL Solution 3........................................................ 0.4mL
Solution 1: Composition per 100.0.0mL:
Preparation of Medium: Aseptically combine 770.0mL of sterile base solution, 100.0mL of heatinactivated bovine serum, 50.0mL of sterile solution A, 50.0mL of sterile solution B, and 30.0mL of sterile special 107 vitamin mix. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation of Entamoeba histolytica.
Absolute ethanol ......................................... 100.0mL DL-6,8-Thioctic acid, oxidized ....................100.0mg
Preparation of Solution 1: Add
Aseptically combine 0.4mL of sterile solution 1, 1.2mL of sterile solution 2, 0.4mL of sterile solution 3, and 100.0mL of sterile solution 4 vitamins. Bring volume to 120.0mL with sterile distilled/deionized water.
DL-6,8-thioctic
acid to absolute ethanol and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Solution 2: Vitamin B12 ....................................................40.0mg
Preparation of Solution 2: Add vitamin B12 to
distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Solution 3: Tween 80...........................................................50.0g Absolute ethanol ......................................... 100.0mL
Preparation of Solution 3: Add Tween 80 to absolute ethanol and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Peptone Iron Agar Composition per liter: Agar ..................................................................15.0g Peptone .............................................................15.0g Proteose peptone.................................................5.0g Sodium glycerophosphate...................................1.0g Ferric ammonium citrate.....................................0.5g Na2S2O3 ............................................................0.08g pH 6.7 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes. Autoclave for 15 min at 15 psi pressure– 121°C. Allow tubes to cool in an upright position.
352
Peptone Meat Extract Soil Extract Agar
Use: For the cultivation and differentiation of microorganisms based on their ability to produce H2S. Microorganisms that produce H2S turn the medium black.
Peptone Meat Extract Soil Extract Agar (PFE Agar) Composition per liter: Agar ..................................................................12.0g Proteose peptone no. 3 ........................................5.0g Meat extract ........................................................3.0g Tap water..................................................... 850.0mL Soil extract .................................................. 150.0mL Glycerol ........................................................ 20.0mL pH 7.0 ± 0.2 at 25°C
Soil Extract: Composition per liter: Garden soil, air dried ......................................400.0g
Preparation of Soil Extract: Pass 400.0g of airdried garden soil through a coarse sieve. Add soil to 960.0mL of tap water. Mix thoroughly. Autoclave for 60 min at 15 psi pressure–121°C. Cool to room temperature. Allow residue to settle. Decant supernatant solution. Filter through Whatman filter paper. Distribute into bottles in 200.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C. Store at room temperature until clear.
Preparation of Medium: Add components to tap
with distilled/deionized water. Autoclave for 12 min at 8 psi pressure–112°C. Pour into sterile Petri dishes or distribute into screw-capped tubes.
Use: For the selective isolation and cultivation of Gardnerella vaginalis.
Peptone Water Composition per liter: Peptone .............................................................10.0g NaCl....................................................................5.0g pH 7.2 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems and Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of nonfastidious microorganisms, for carbohydrate fermentation tests, and for performing the indole test.
Peptone Water with Andrade’s Indicator Composition per liter:
water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure– 121°C. Pour into sterile Petri dishes or leave in tubes.
Peptone .............................................................10.0g NaCl....................................................................5.0g Andrade’s indicator..................................... 100.0mL Carbohydrate solution................................... 20.0mL pH 7.4 ± 0.2 at 25°C
Use: For the cultivation and maintenance of Mycobac-
Source: This medium is available as a premixed
terium avium, Mycobacterium gastri, Mycobacterium kansasii, Mycobacterium marinum, Mycobacterium scrofulaceum, and Mycobacterium terrae.
powder from Oxoid Unipath.
Peptone Starch Dextrose Agar (PSD Agar) (Dunkelberg Agar) Composition per liter: Proteose peptone no. 3 ......................................20.0g Agar ..................................................................15.0g Soluble starch....................................................10.0g Glucose ...............................................................2.0g Na2HPO4 .............................................................1.0g NaH2PO4 .............................................................1.0g pH 6.8 ± 0.2 at 25°C
Andrade’s Indicator: Composition per 100.0mL: NaOH (1N solution) ..................................... 16.0mL Acid Fuchsin......................................................0.1 g
Caution: Acid Fuchsin is a potential carcinogen and care must be taken to avoid inhalation of the powdered dye and contact with the skin.
Carbohydrate Solution: Composition per 20.0mL: Carbohydrate..............................................5.0–10.0g
Preparation of Carbohydrate Solution: Add carbohydrate to distilled/deionized water and bring volume to 20.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add starch to approxi-
Preparation of Medium: Add components, ex-
mately 100.0mL of cold distilled/deionized water. Mix thoroughly. Add starch solution to 400.0mL of boiling distilled/deionized water. Add remaining components. Mix thoroughly. Bring volume to 1.0L
cept carbohydrate solution, to distilled/deionized water and bring volume to 980.0mL. Mix thoroughly. Adjust pH to 7.4 if necessary. Distribute into tubes containing an inverted Durham tube. Fill each tube
Pfizer Selective Enterococcus Agar with 9.8mL of medium. Autoclave for 15 min at 15 psi pressure–121°C. Aseptically add 0.2mL of sterile carbohydrate solution to each tube.
Use: For use in carbohydrate fermentation tests. Fermentation is determined by the production of acid— broth turns pink—and formation of gas—bubble trapped in Durham tube.
Peptone Yeast Trypticase Agar (ATCC Medium 118)
353
another sterile container. Measure out 121.0mL. Aseptically add homogenized whole egg and egg yolk to cooled sterile basal medium. Mix thoroughly. Aseptically distribute into sterile tubes. Inspissate at 85°–90°C (moist heat) for 45 min.
Use: For the isolation and cultivation of Mycobacterium species from clinical specimens.
Petragnani Medium Composition per 2285.0mL:
Agar ..................................................................15.0g Peptone................................................................6.0g Trypticase (pancreatic digest of casein)..............4.0g Yeast extract........................................................3.0g Beef extract .........................................................1.5g Glucose ...............................................................1.0g pH 7.0 ± 0.2 at 25°C
Potato ..............................................................500.0g Potato flour .......................................................36.0g Malachite Green..................................................1.2g Whole egg................................................. 1200.0mL Whole milk ................................................. 900.0mL Egg yolk...................................................... 115.0mL Glycerol ........................................................ 70.0mL pH 7.2 ± 0.2 at 25°C
Preparation of Medium: Add components to
Source: This medium is available as a prepared me-
Composition per liter:
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation of a variety of heterotrophic bacteria.
Petragnani Medium Composition per 2398.0mL: Skim milk........................................................100.0g Potato flour .......................................................36.4g L-Asparagine .......................................................5.1g Pancreatic digest of casein..................................5.1g Malachite Green..................................................1.2g Whole egg ................................................. 1277.0mL Egg yolk...................................................... 121.0mL Glycerol ........................................................ 60.0mL pH 7.0 ± 0.2 at 25°C
Source: This medium is available as a prepared medium from BD Diagnostic Systems.
Preparation of Medium: Add components—except whole egg, egg yolk, and glycerol—to distilled/ deionized water and bring volume to 940.0mL. Mix thoroughly. Add glycerol. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Scrub the eggshells with soap. Let stand in a soap solution for 30 min. Rinse in running water. Soak eggs in 70% ethanol for 15 min. Break the eggs into a sterile container. Homogenize by shaking. Filter through four layers of sterile cheesecloth into a sterile graduated cylinder. Measure out 1277.0mL. Add separated egg yolks to
dium from BD Diagnostic Systems.
Preparation of Medium: Peel and dice potato. Add potato to 500.0mL of distilled/deionized water. Gently heat and bring to boiling. Continue boiling for 30 min. Filter solids through two layers of cheesecloth. Combine potato solids with remaining components, except whole egg, egg yolk, and glycerol. Mix thoroughly. Add glycerol. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Scrub the eggshells with soap. Let stand in a soap solution for 30 min. Rinse in running water. Soak eggs in 70% ethanol for 15 min. Break the eggs into a sterile container. Homogenize by shaking. Filter through four layers of sterile cheesecloth into a sterile graduated cylinder. Measure out 1200.0mL. Add separated egg yolks to another sterile container. Measure out 115.0mL. Aseptically add homogenized whole egg and egg yolk to cooled sterile basal medium. Mix thoroughly. Aseptically distribute into sterile tubes. Inspissate at 85°–90°C (moist heat) for 45 min. Use: For the isolation and cultivation of Mycobacterium species from clinical specimens.
Pfizer Selective Enterococcus Agar (PSE Agar) Peptone C..........................................................17.0g Agar ..................................................................15.0g Bile....................................................................10.0g NaCl....................................................................5.0g Yeast extract........................................................5.0g Peptone B............................................................3.0g Esculin ................................................................1.0g Sodium citrate.....................................................1.0g
354
PGA
Ferric ammonium citrate.....................................0.5g NaN3 .................................................................0.25g pH 7.1 ± 0.2 at 25°C
Caution: Sodium azide is toxic. Azides also react with metals and disposal must be highly diluted.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the selective isolation, cultivation, and enumeration of Enterococcus species by the multiple tube technique.
PGA (Potato Glucose Agar) Composition per liter: Potatoes...........................................................500.0g Glucose .............................................................20.0g Agar ..................................................................15.0g Yeast extract........................................................5.0g
L-Glutamic
acid...................................................0.5g MgSO4·7H2O ....................................................0.45g Maltose ...............................................................0.2g L-Cystine .............................................................0.2g DL-Tryptophan.....................................................0.1g Solution 3.................................................... 100.0mL Solution 2........................................................ 2.0mL Calcium pantothenate (0.1% solution) ........... 0.5mL pH 6.8 ± 0.2 at 25°C
Solution 3: Composition per 500.0mL: Maltose ...........................................................200.0g CaCl2 ...................................................................1.5g Calcium pantothenate (0.1% solution) ........... 3.0mL FeSO4 (1% in 1N HCl) ................................... 0.2mL
Preparation of Solution 3: Add components to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Autoclave for 15 min at 7 psi pressure–111°C. Cool to 45°–50°C.
Solution 2: Composition per 100.0mL: β-Alanine........................................................ 0.115g
Preparation of Medium: Slice potatoes with skin. Place 500.0g of potatoes in 1.0L of distilled/ deionized water. Gently heat and bring to boiling. Allow to boil for 20 min. Filter through Whatman filter paper. Add agar and other components to filtrate. Bring volume to 1.0L with distilled/deionized water. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Nicotinic acid.................................................. 0.115g CuSO4·5H2O .....................................................0.05g ZnSO4·7H2O ...................................................0.045g MnCl2·4H2O ...................................................0.015g Pimelic acid .....................................................7.5mg HCl, concentrated ........................................... 3.0mL
Use: For the cultivation of numerous filamentous
Preparation of Medium: Add components, except
fungi.
PGP Broth (Peptone Glycerol Phosphate Broth) Composition per liter: Peptone................................................................5.0g K2HPO4 ...............................................................2.0g Glycerol ........................................................ 10.0mL
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation and maintenance of Serratia marcescens.
PGT Medium
Preparation of Solution 2: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. solution 3, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Adjust pH to 6.8 with 50% KOH. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile solution 3. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation and maintenance of Corynebacterium diphtheriae.
Phenol Red Agar Composition per liter: Agar ..................................................................15.0g Pancreatic digest of casein................................10.0g NaCl....................................................................5.0g Phenol Red......................................................0.018g Carbohydrate solution................................... 20.0mL pH 7.4 ± 0.2 at 25°C
Composition per liter:
Source: This medium is available as a premixed
Casamino acids .................................................30.0g
powder from BD Diagnostic Systems.
Phenol Red Lactose Agar Carbohydrate Solution: Composition per 20.0mL:
355
Carbohydrate..............................................5.0–10.0g
Phenol Red......................................................0.018g Carbohydrate solution................................... 20.0mL pH 7.4 ± 0.2 at 25°C
Preparation of Carbohydrate Solution: Add
Source: This medium is available as a premixed
carbohydrate to distilled/deionized water and bring volume to 20.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except carbohydrate solution, to distilled/deionized water and bring volume to 980.0mL. Mix thoroughly. Adjust pH to 7.4 if necessary. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 20.0mL of sterile carbohydrate solution. Pour into sterile Petri dishes or distribute into sterile tubes. Allow tubes to cool in a slanted position.
Use: For the determination of fermentation reactions. Bacteria that can ferment the added carbohydrate turn the medium yellow.
Phenol Red Agar Composition per liter: Agar ..................................................................15.0g Proteose peptone no. 3 ......................................10.0g NaCl ....................................................................5.0g Beef extract .........................................................1.0g Phenol Red......................................................0.025g Carbohydrate solution................................... 20.0mL pH 7.4 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
powder from BD Diagnostic Systems.
Carbohydrate Solution: Composition per 20.0mL: Carbohydrate..............................................5.0–10.0g
Preparation of Carbohydrate Solution: Add carbohydrate to distilled/deionized water and bring volume to 20.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except carbohydrate solution, to distilled/deionized water and bring volume to 980.0mL. Mix thoroughly. Adjust pH to 7.4 if necessary. Distribute into tubes containing an inverted Durham tube. Fill each tube with 9.8mL of medium. Autoclave for 15 min at 13 psi pressure–118°C. Cool to 45°–50°C. Aseptically add 0.2mL of sterile carbohydrate solution to each tube.
Use: For the determination of fermentation reactions in the differentiation of microorganisms. Fermentation is determined by the production of acid—broth turns yellow—and formation of gas—bubble trapped in Durham tube.
Phenol Red Glucose Broth Composition per liter:
Carbohydrate..............................................5.0–10.0g
Pancreatic digest of casein................................10.0g Glucose ...............................................................5.0g NaCl....................................................................5.0g Phenol Red......................................................0.018g pH 7.3 ± 0.2 at 25°C
Preparation of Carbohydrate Solution: Add
Source: This medium is available as a premixed
carbohydrate to distilled/deionized water and bring volume to 20.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components to
Carbohydrate Solution: Composition per 20.0mL:
Preparation of Medium: Add components, except carbohydrate solution, to distilled/deionized water and bring volume to 980.0mL. Mix thoroughly. Adjust pH to 7.4 if necessary. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 20.0mL of sterile carbohydrate solution. Pour into sterile Petri dishes or distribute into sterile tubes. Allow tubes to cool in a slanted position.
Use: For the determination of fermentation reactions. Bacteria that can ferment the added carbohydrate turn the medium yellow.
Phenol Red Broth Composition per liter: Pancreatic digest of casein................................10.0g NaCl ....................................................................5.0g
powder from BD Diagnostic Systems. distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.3 if necessary. Distribute into tubes containing an inverted Durham tube. Fill each tube with 10.0mL of medium. Autoclave for 15 min at 13 psi pressure–118°C.
Use: For determination of the ability of a microorganism to ferment glucose. Fermentation is determined by the production of acid—broth turns yellow—and formation of gas—bubble trapped in Durham tube.
Phenol Red Lactose Agar Composition per liter: Agar ..................................................................15.0g Lactose..............................................................10.0g Proteose peptone no. 3......................................10.0g
356
Phenol Red Lactose Broth
NaCl ....................................................................5.0g Beef extract .........................................................1.0g Phenol Red.....................................................25.0mg pH 7.4 ± 0.2 at 25°C
thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 13 psi pressure–118°C. Pour into sterile Petri dishes or leave in tubes. Allow tubes to cool in a slanted position.
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Use: For determination of the ability of a microor-
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 13 psi pressure–118°C. Pour into sterile Petri dishes or leave in tubes. Allow tubes to cool in a slanted position.
Use: For determination of the ability of a microorganism to ferment lactose. Fermentation is determined by the production of acid—medium turns yellow.
Phenol Red Lactose Broth Composition per liter: Pancreatic digest of casein................................10.0g Lactose ................................................................5.0g NaCl ....................................................................5.0g Phenol Red......................................................0.018g pH 7.3 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.3 if necessary. Distribute into tubes containing an inverted Durham tube. Fill each tube with 10.0mL of medium. Autoclave for 15 min at 13 psi pressure–118°C.
Use: For determination of the ability of a microor-
ganism to ferment mannitol. Fermentation is determined by the production of acid—medium turns yellow.
Phenol Red Mannitol Broth Composition per liter: Pancreatic digest of casein................................10.0g D-Mannitol..........................................................5.0g NaCl....................................................................5.0g Phenol Red......................................................0.018g pH 7.3 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.3 if necessary. Distribute into tubes containing an inverted Durham tube. Fill each tube with 10.0mL of medium. Autoclave for 15 min at 13 psi pressure–118°C.
Use: For determination of the ability of a microorganism to ferment mannitol. Fermentation is determined by the production of acid—broth turns yellow—and formation of gas—bubble trapped in Durham tube.
Phenol Red Sucrose Broth Composition per liter:
ganism to ferment lactose. Fermentation is determined by the production of acid—broth turns yellow—and formation of gas—bubble trapped in Durham tube.
Pancreatic digest of casein................................10.0g NaCl....................................................................5.0g Sucrose................................................................5.0g Phenol Red......................................................0.018g pH 7.3 ± 0.2 at 25°C
Phenol Red Mannitol Agar
Source: This medium is available as a premixed
Composition per liter: Agar ..................................................................15.0g Mannitol............................................................10.0g Proteose peptone no. 3 ......................................10.0g NaCl ....................................................................5.0g Beef extract .........................................................1.0g Phenol Red.....................................................25.0mg pH 7.4 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix
powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.3 if necessary. Distribute into tubes containing an inverted Durham tube. Fill each tube with 10.0mL of medium. Autoclave for 15 min at 13 psi pressure–118°C.
Use: For determination of the ability of a microorganism to ferment sucrose. Fermentation is determined by the production of acid—broth turns yellow—and formation of gas—bubble trapped in Durham tube.
Phenylethanol Agar
Phenol Red Tartrate Agar Composition per liter: Agar ..................................................................15.0g Peptone..............................................................10.0g Potassium tartrate..............................................10.0g NaCl ....................................................................5.0g Phenol Red......................................................0.024g pH 7.6 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components to cold distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 13 psi pressure–118°C. Pour into sterile Petri dishes or leave in tubes. Allow tubes to cool in an upright position.
Use: For the differentiation of Gram-negative bacteria of the intestinal groups, particularly members of the Salmonella (paratyphoid) group based on their ability to ferment tartrate.
Phenol Red Tartrate Broth Composition per liter:
357
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Distribute into tubes or flasks. Autoclave for 10 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the differentiation of enteric Gram-negative bacilli on the basis of their ability to produce phenylpyruvic acid from phenylalanine. After appropriate incubation of bacteria, ferric chloride reagent is added on the agar. Formation of a green color in 1– 5 min indicates the production of phenylpyruvic acid.
Phenylalanine Malonate Broth Composition per liter: Sodium malonate ................................................3.0g DL-Phenylalanine ................................................2.0g NaCl....................................................................2.0g (NH4)2SO4 ..........................................................2.0g Yeast extract........................................................1.0g K2HPO4...............................................................0.6g KH2PO4...............................................................0.4g Bromthymol Blue ...........................................0.025g pH 7.3 ± 0.2 at 25°C
Pancreatic digest of casein................................10.0g Potassium tartrate..............................................10.0g Agar ....................................................................5.0g NaCl ....................................................................5.0g Phenol Red......................................................0.024g pH 7.6 ± 0.2 at 25°C
Source: This medium is available as a premixed
Preparation of Medium: Add components to
Use: For the differentiation of Gram-negative enter-
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the differentiation of Gram-negative bacteria of the intestinal groups, particularly members of the Salmonella (paratyphoid) group based on their ability to ferment tartrate.
Phenylalanine Agar (Phenylalanine Deaminase Medium) Composition per liter: Agar ..................................................................12.0g NaCl ....................................................................5.0g Yeast extract........................................................3.0g DL-Phenylalanine.................................................2.0g Na2HPO4 .............................................................1.0g pH 7.3 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 10 min at 10 psi pressure–115°C. ic bacilli on the basis of malonate utilization and formation of pyruvic acid from phenylalanine.
Phenylethanol Agar Composition per liter: Agar ..................................................................15.0g Tryptose ............................................................10.0g NaCl....................................................................5.0g Beef extract.........................................................3.0g Phenylethanol .....................................................2.5g pH 7.3 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
358
Phenylethanol Blood Agar
Use: For the isolation of staphylococci and streptococci from specimens containing a mixed flora.
Thiamine Pyrophosphate Solution: Composition per 10.0mL: Thiamine pyrophosphate ..................................0.05g
Phenylethanol Blood Agar Composition per liter: Agar ..................................................................15.0g Tryptose ............................................................10.0g NaCl ....................................................................5.0g Beef extract .........................................................3.0g Phenylethanol......................................................2.5g Blood, defibrinated ....................................... 50.0mL pH 7.3 ± 0.2 at 25°C
Preparation of Medium: Add components, except blood, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 13 psi pressure–118°C. Cool to 45°–50°C. Aseptically add sterile defibrinated blood. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation of staphylococci and streptococci from specimens containing a mixed flora.
PHYG Medium Composition per 110.1mL: Beef heart, solids from infusion........................10.0g Polypeptone ........................................................2.0g Gelatin.................................................................1.0g Glucose ...............................................................1.0g Yeast extract........................................................1.0g NaHCO3 ..............................................................0.5g Tryptose ..............................................................0.2g Agar ..................................................................0.16g NaCl ....................................................................0.1g L-Cysteine·HCl·H2O .........................................0.09g (NH4)2SO4.........................................................0.05g Resazurin .......................................................0.16mg Salts solution................................................. 50.0mL Rabbit serum, inactivated ............................. 10.0mL Thiamine pyrophosphate solution................... 0.1mL pH 7.2–7.5 at 25°C
Salts Solution: Composition per 400.0mL: K2HPO4 ...............................................................0.9g NaCl ....................................................................0.8g KH2PO4 ...............................................................0.4g MnCl2·4H2O .....................................................0.16g MgSO4 ..............................................................0.08g
Preparation of Salts Solution: Add components to distilled/deionized water and bring volume to 400.0mL. Mix thoroughly.
Preparation of Thiamine Pyrophosphate Solution: Add thiamine pyrophosphate to distilled/ deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except rabbit serum and thiamine pyrophosphate solution, to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C. Aseptically add 10.0mL of sterile rabbit serum and 0.1mL of sterile thiamine pyrophosphate solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation of treponemes.
Pike Streptococcal Broth Composition per liter: Pancreatic digest of casein................................10.0g Tryptose ............................................................10.0g Yeast extract......................................................10.0g Glucose ...............................................................0.2g NaN3 ...............................................................0.065g Crystal Violet ...................................................2.0mg Rabbit blood, defibrinated ............................ 50.0mL pH 7.4 ± 0.2 at 25°C
Caution: Sodium azide is toxic. Azides also react with metals and disposal must be highly diluted.
Preparation of Medium: Add components, except rabbit blood, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Distribute into flasks in 100.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 5.0mL of sterile rabbit blood to each flask. Mix thoroughly.
Use: For the isolation and enrichment of hemolytic streptococci from throat swabs and other clinical specimens. After incubation of bacteria for 18–24h in this medium, they may be isolated by streaking the culture onto blood agar plates.
Pine and Drouhet’s Histoplasma Yeast Phase Medium Composition per liter: Casein hydrolysate-vitaminglucose base.......................................... 500.0mL Agar starch base.......................................... 500.0mL
Pine and Drouhet’s Histoplasma Yeast Phase Medium
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Casein Hydrolysate-Vitamin-Glucose Base: Composition per 500.0mL:
Nicotinamide.......................................................0.1g Biotin .............................................................10.0mg
Glucose .............................................................10.0g Citric acid..........................................................10.0g L-Cysteine·HCl ...................................................1.0g L-Asparagine.......................................................1.0g Glutathione, reduced...........................................0.5g L-Tryptophan ....................................................0.02g Solution 1.................................................... 250.0mL Solution 2...................................................... 10.0mL Solution 3...................................................... 40.0mL Solution 4...................................................... 10.0mL Solution 5........................................................ 1.0mL Solution 6........................................................ 0.1mL Solution 7........................................................ 0.1mL
Preparation of Solution 4: Add components to
Solution 1: Composition per liter: KH2PO4 ...............................................................8.0g (NH4)2SO4...........................................................8.0g MgSO4·7H2O ....................................................0.86g CaCl2 .................................................................0.08g
Preparation of Solution 1: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Store at 5°C.
Solution 2: Composition per liter: FeSO4·7H2O........................................................5.7g MnCl2·6H2O .......................................................0.8g Na2MoO4·2H2O ................................................0.15g HCl, concentrated ........................................... 1.0mL
Preparation of Solution 2: Add the concentrated HCl to 100.0mL of distilled/deionized water. Add FeSO4·7H2O, MnCl2·6H2O, and Na2MoO4·2H2O, in that order. Make sure each salt is completely dissolved before adding the next. Mix thoroughly. Bring volume to 1.0L with distilled/deionized water. Mix thoroughly. Store at 5°C. Solution is good until a red precipitate forms.
Solution 3 Composition per 100.0mL: Acid hydrolysate of casein, vitamin free.......10.0g Preparation of Solution 3: Add acid hydrolysate of casein to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Gently heat until dissolved.
Solution 4: Composition per liter: Inositol ................................................................0.2g Thiamine·HCl .....................................................0.2g Calcium pantothenate .........................................0.2g Riboflavin ...........................................................0.2g
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Store at 5°C. Suspension is good for 6 months to 1 year.
Solution 5: Composition per 100.0mL: Hemin .................................................................0.2g NH4OH, concentrated solution .................. 2–3 drops
Preparation of Solution 5: Add hemin to 10.0mL of distilled/deionized water. Dissolve by adding a few drops of concentrated NH4OH. Mix thoroughly. Bring volume to 100.0mL with distilled/ deionized water. Store at 5°C. Solution 6 Composition per 100.0mL: DL-Thioctic acid ............................................10.0mg
Ethanol (95% solution) ................................. 10.0mL
Preparation of Solution 6: Add thioctic acid to 10.0mL of 95% ethanol. Mix thoroughly. Store at −20°C. Solution 7: Composition per 10.0mL: Coenzyme A ..................................................10.0mg Na2S·5H2O (0.05% solution in freshly boiled, distilled/deionized H2O).......................... 2 drops
Preparation of Solution 7: Add coenzyme A to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Add 2 drops of 0.05% Na2S·5H2O solution. Store at −20°C. Preparation of Casein Hydrolysate-VitaminGlucose Base: Add components to distilled/ deionized water and bring volume to 450.0mL. Mix thoroughly. Adjust pH to 6.5 with 20% KOH solution. Bring volume to 500.0mL with distilled/ deionized water. Mix thoroughly. Filter sterilize.
Agar Starch Base: Composition per 500.0mL: Agar ..................................................................12.5g Potato starch, insoluble.......................................2.0g Solution 8...................................................... 10.0mL
Solution 8: Composition per 100.0mL: Oleic acid ............................................................0.1g
Preparation of Solution 8: Add oleic acid to distilled/deionized water and bring volume to 50.0mL. Mix thoroughly. Adjust pH to 7.0 with NaOH. Bring volume to 100.0mL with distilled/deionized water.
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Pisu Medium
Preparation of Agar Starch Base: Add potato starch to distilled/deionized water and bring volume to 50.0mL. Mix thoroughly. Pour into 440.0mL of boiling, distilled/deionized water. Add 10.0mL of solution 8 and the agar. Mix thoroughly. Autoclave for 20 min at 15 psi pressure–121°C. Preparation of Medium: Aseptically combine 500.0mL of filter-sterilized casein hydrolysate-vitamin-glucose base with 500.0mL of hot agar starch base. Mix thoroughly. Heat nearly to boiling while stirring constantly. Aseptically distribute into sterile tubes. Allow tubes to cool in a slanted position. Use: For the cultivation and maintenance of Blastomyces dermatitidis and Histoplasma capsulatum in the yeast phase.
Pisu Medium Composition per 1512.0mL: Agar base .................................................... 960.0mL Horse serum, sterile .................................... 360.0mL L-Cystine solution....................................... 180.0mL Lead acetate solution .................................... 12.0mL pH 6.8 ± 0.2 at 25°C
Agar Base: Composition per liter: Proteose peptone no. 3 ......................................20.0g Agar ....................................................................7.0g NaCl ....................................................................5.0g Meat extract ........................................................4.0g
Preparation for Agar Base: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Dissolve in steam for 15 min at 0 psi pressure–100°C. Cool to 45°–50°C. Adjust pH to 7.5. Filter sterilize. Distribute into 200.0mL Erlenmeyer flasks in 80.0mL volumes. Autoclave for 60 min at 0 psi pressure–100°C. Cool to 60°C. L-Cystine
Solution: Composition per 200.0mL: L-Cystine .............................................................2.0g
Preparation of L-Cystine Solution: Add L-cystine to distilled/deionized water and bring volume to 200.0mL. Mix thoroughly. Filter sterilize.
Lead Acetate Solution: Composition per 100.0mL: Lead acetate ......................................................10.0g
Preparation of Lead Acetate Solution: Add lead acetate to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation for Medium: To each flask containing 80.0mL of cooled, sterile agar base, aseptically add 30.0mL of sterile horse serum, 15.0mL of sterile
L-cystine solution, and 1.0mL of sterile lead acetate solution. Mix thoroughly. Aseptically distribute into small sterile tubes in 2.0–3.0mL volumes.
Use: For the cultivation and differentiation of bacteria based on their ability to produce cystinase. Cystinase-producing bacteria turn the medium black.
PKU Test Agar (Phenylketonuria Test Agar) Composition per liter: Agar ..................................................................15.0g K2HPO4.............................................................15.0g Glucose .............................................................10.0g KH2PO4...............................................................5.0g (NH4)Cl...............................................................2.5g (NH4)NO3 ...........................................................0.5g Asparagine ..........................................................0.5g DL-Alanine ..........................................................0.5g L-Glutamic acid...................................................0.5g Na2SO4 ................................................................0.5g MgSO4·7H2O ....................................................0.05g FeCl3 ................................................................5.0mg MnCl2·4H2O ....................................................5.0mg β-2-Thienylalanine ..........................................3.3mg CaCl2·2H2O .....................................................2.5mg Bacillus subtilis spore suspension ................ 10.0mL pH 7.0 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Continue boiling for 5 min. Do not autoclave. Cool to 50°C. Add 10.0mL of a suspension of Bacillus subtilis ATCC 6633 spores. Mix thoroughly. Pour into sterile Petri dishes or other containers.
Use: For the determination of phenylalanine concentrations in serum or urine. Used in the Guthrie-modified bacterial-inhibition assay procedure for screening newborn infants for phenylketonuria (PKU).
PKU Test Agar (Phenylketonuria Test Agar) Composition per liter: K2HPO4.............................................................15.0g Agar ..................................................................13.5g Glucose ...............................................................5.0g KH2PO4...............................................................5.0g (NH4)Cl...............................................................2.5g L-Asparagine .......................................................0.5g L-Glutamic acid...................................................0.5g
PLET Agar
Na2SO4 ................................................................0.5g (NH4)NO3 ...........................................................0.5g L-Alanine...........................................................0.25g MgSO4·7H2O ....................................................0.05g FeCl3 ...............................................................0.005g MnSO4· ............................................................0.005g CaCl2·2H2O......................................................2.5mg β-2-Thienylalanine solution............................ 1.0mL pH 6.9 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. β-2-Thienylalanine Solution: Composition per 100.0mL:
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coli can be identified by fluorescence in the UV and verified by means of a positive indole test.
Plate Count MUG Agar Composition per liter: Agar ..................................................................14.0g Casein peptone....................................................5.0g Yeast extract........................................................2.5g D(+)-Glucose.......................................................1.0g Tryptophan..........................................................1.0g 4-Methylumbelliferyl-β-D-glucuronide ............0.07g pH 7.0 ± 0.2 at 37°C
Source: This medium is available from Fluka, Sig-
β-2-Thienylalanine............................................0.33g
ma-Aldrich.
Preparation of β-2-Thienylalanine Solution:
Preparation of Medium: Add components to
Add β-2-thienylalanine to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, ex-
cept β-2-thienylalanine solution, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Continue boiling for 5 min. Do not autoclave. Cool to 50°C. Add 10.0mL of a suspension of Bacillus subtilis ATCC 6633 spores and 1.0mL of sterile β-2-thienylalanine solution. Mix thoroughly. Pour into sterile Petri dishes or other containers.
Use: For the determination of phenylalanine concentrations in serum or urine. Used in the Guthrie-modified bacterial-inhibition assay procedure for screening newborn infants for phenylketonuria (PKU).
Plate Count MUG Agar Composition per liter:
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 50°C. Pour into sterile Petri dishes.
Use: For the determination of bacterial counts in milk, dairy products, water, and other material. E. coli can be identified by fluorescence in the UV and verified by means of a positive indole test.
PLET Agar Composition per liter: Beef heart, solids from infusion......................500.0g Agar ..................................................................15.0g Tryptose ............................................................10.0g NaCl....................................................................5.0g Ethylenediamine tetracetic acid (EDTA)............0.3g Thallous acetate ................................................0.04g Antibiotic inhibitor ....................................... 10.0mL
Agar ..................................................................14.0g Casein peptone....................................................5.0g Yeast extract........................................................2.5g D(+)-Glucose.......................................................1.0g Tryptophan ..........................................................1.0g 4-Methylumbelliferyl-β-D-glucuronide ............0.07g pH 7.0 ± 0.2 at 37°C
Antibiotic Inhibitor: Composition per 10.0mL:
Source: This medium is available from Fluka, Sig-
Preparation of Medium: Add components, ex-
ma-Aldrich.
Lysozyme................................................... 300,000U Polymyxin.................................................... 30,000U
Preparation of Antibiotic Inhibitor: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 50°C. Pour into sterile Petri dishes.
cept antibiotic inhibitor, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C. Aseptically add sterile antibiotic inhibitor. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the determination of bacterial counts in
Use: For the selective isolation and cultivation of
milk, dairy products, water, and other material. E.
Bacillus anthracis.
Preparation of Medium: Add components to
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Poly-β-Hydroxybutyrate Medium
Poly-β-Hydroxybutyrate Medium (PHB Medium) Composition per liter: Part A .......................................................... 900.0mL Part B .......................................................... 100.0mL pH 7.2 ± 0.2 at 25°C
Part A: Composition per 900.0mL: K2HPO4·3H2O.....................................................0.6g KH2PO4 ...............................................................0.2g MgSO4·7H2O ......................................................0.2g (NH4)2SO4...........................................................0.2g
Preparation of Medium: Add components to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Adjust pH to 7.2. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C.
Part B: Composition per 100.0mL: Glucose .............................................................10.0g
Preparation of Medium: Add glucose to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C.
Preparation of Medium: Aseptically combine 900.0mL of cooled, sterile part A and 100.0mL of cooled, sterile part B. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation and differentiation of Pseudomonas species based on their ability to produce intracellular poly-β-hydroxybutyrate. Production of poly-β-hydroxybutyrate is determined by staining cells with Sudan Black B.
Polymyxin Staphylococcus Medium Composition per liter: Agar ..................................................................15.0g Pancreatic digest of gelatin .................................5.0g Beef extract .........................................................3.0g Lecithin ...............................................................0.7g Polymyxin.......................................................0.075g Tween 80....................................................... 10.2mL pH 6.8 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes.
Use: For the selective isolation and cultivation of pathogenic, coagulase-positive Staphylococcus au-
reus. Proteus species will grow on this medium but appear as translucent colonies.
Porcine Heart Agar Composition per liter: Porcine heart, infusion from ...........................375.0g Agar ..................................................................15.0g Papaic digest of soybean meal............................6.5g Glucose ...............................................................5.0g NaCl....................................................................5.0g Proteose peptone no. 3........................................5.0g Yeast extract........................................................3.5g Sheep blood, defibrinated ............................. 50.0mL pH 7.2 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components, except sheep blood, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile sheep blood. Mix thoroughly. Pour into sterile Petri dishes.
Use: For determination of the sensitivity of microorganisms to antimicrobics using the disc plate technique.
Potassium Cyanide Broth Composition per liter: Na2HPO4 ...........................................................5.64g NaCl....................................................................5.0g Proteose peptone no. 3........................................3.0g KH2PO4...........................................................0.225g KCN solution ................................................ 15.0mL pH 7.6 ± 0.2 at 25°C
KCN Solution: Composition per 100.0mL: KCN....................................................................0.5g
Preparation of KCN Solution: Add KCN to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly.
Caution: Cyanide is toxic. Preparation of Medium: Add components, except KCN solution, to distilled/deionized water and bring volume to 985.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C. Aseptically add 15.0mL of KCN solution. Mix thoroughly. Distribute into sterile screw-capped tubes or flasks in 1.0– 1.5mL volumes. Close caps tightly.
PPLO Agar Use: For the cultivation and differentiation of ureasenegative, Gram-negative enteric bacteria. Salmonella species and Shigella species are nonmotile in this medium. Proteus species are motile in this medium.
Potassium Tellurite Agar
363
Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of Bacillus species and fungi.
Composition per liter: Beef heart, solids from infusion......................500.0g Agar ..................................................................15.0g Tryptose ............................................................10.0g NaCl ....................................................................5.0g Blood, defibrinated ....................................... 50.0mL K2TeO3 solution ............................................ 20.0mL pH 6.0 ± 0.2 at 25°C
K2TeO3 Solution: Composition per 20.0mL: K2TeO3 ................................................................0.5g
Preparation of K2TeO3 Solution: Add K2TeO3
Potato Extract Agar Composition per liter: Agar ..................................................................15.0g Peptone ...............................................................5.0g NaCl....................................................................5.0g Yeast extract........................................................2.0g Beef extract powder............................................1.0g Potato extract ................................................ 20.0mL pH 7.4 ± 0.2 at 25°C
Potato Extract: Composition per liter:
to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Potatoes...........................................................300.0g
Caution: Potassium tellurite is toxic.
potatoes. Add 500.0mL of distilled/deionized water. Gently heat and bring to boiling. Continue boiling for 30 min. Filter through cheesecloth.
Preparation of Medium: Add components, except K2TeO3 solution, to distilled/deionized water and bring volume to 930.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile K2TeO3 solution and 50.0mL of blood. Rabbit or sheep blood may be used. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes. Allow tubes to cool in a slanted position.
Use: For the cultivation and differentiation of Enterococcus faecalis. Enterococcus faecalis appears as black colonies.
Potato Dextrose Yeast Agar (PDY Agar) Composition per liter: Glucose .............................................................20.0g Agar ..................................................................15.0g Yeast extract........................................................5.0g Potato infusion ............................................ 500.0mL pH 5.6 ± 0.2 at 25°C
Potato Infusion: Composition per 500.0mL: Potatoes...........................................................300.0g
Preparation of Potato Extract: Peel and dice
Use: For the cultivation of a wide variety of yeasts and molds.
PPLO Agar Composition per liter: Beef heart, infusion from..................................50.0g Agar ..................................................................14.0g Peptone .............................................................10.0g NaCl....................................................................5.0g Bovine serum .............................................. 100.0mL pH 7.8 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components, except bovine serum, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile bovine serum. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation and cultivation of Mycoplasma species (pleuro-pneumonia-like organisms).
Preparation of Potato Infusion: Peel and dice potatoes. Add 500.0mL of distilled/deionized water. Gently heat and bring to boiling. Continue boiling for 30 min. Filter through cheesecloth. Reserve filtrate.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L.
PPLO Agar Composition per liter: Beef heart, infusion from..................................50.0g Agar ..................................................................14.0g Peptone .............................................................10.0g
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PPLO Broth with Crystal Violet
NaCl ....................................................................5.0g Ascitic fluid................................................. 250.0mL pH 7.8 ± 0.2 at 25°C
Penicillin (optional) ................................... 100,000U Ascitic fluid ................................................ 250.0mL pH 7.8 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Source: This medium is available as a premixed
Preparation of Medium: Add components, ex-
Preparation of Medium: Add components, ex-
cept ascitic fluid, to distilled/deionized water and bring volume to 750.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile ascitic fluid. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation and cultivation of Mycoplasma species (pleuro-pneumonia-like organisms).
PPLO Broth with Crystal Violet Composition per liter: Beef heart, infusion from ..................................50.0g Peptone..............................................................10.0g NaCl ....................................................................5.0g Crystal Violet ....................................................0.01g Ascitic fluid................................................. 250.0mL Chapman tellurite solution............................ 2.85mL pH 7.8 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Chapman Tellurite Solution: Composition per 100.0mL: K2TeO3 ................................................................1.0g
Preparation of Chapman Tellurite Solution: Add K2TeO3 to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Caution: Potassium tellurite is toxic. Preparation of Medium: Add components, except ascitic fluid and Chapman tellurite solution, to distilled/deionized water and bring volume to 747.15mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to less than 37°C. Aseptically add sterile ascitic fluid and 2.85mL of Chapman tellurite solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the isolation of Mycoplasma species from clinical specimens.
PPLO Broth without Crystal Violet Composition per liter: Beef heart, infusion from ..................................50.0g Peptone..............................................................10.0g NaCl ....................................................................5.0g Thallium acetate (optional).................................0.5g
powder from BD Diagnostic Systems. cept ascitic fluid, to distilled/deionized water and bring volume to 750.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to less than 37°C. Aseptically add sterile ascitic fluid. If desired, 0.5g of thallium acetate or 100,000U of penicillin may be added for a more selective medium. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the enrichment of pleuro-pneumonia-like organisms (PPLOs) and Mycoplasma species from clinical specimens.
PPLO Broth without Crystal Violet with Calf Serum, Fresh Yeast Extract, and Sodium Acetate Composition per liter: Beef heart, infusion from..................................50.0g Peptone .............................................................10.0g Sodium acetate....................................................9.0g NaCl....................................................................5.0g Yeast extract solution, fresh........................ 250.0mL Calf serum................................................... 100.0mL pH 7.8 ± 0.2 at 25°C
Yeast Extract Solution: Composition per 300.0mL: Baker’s yeast, live, pressed, starch-free............75.0g
Preparation of Yeast Extract Solution: Add the live Baker’s yeast to 300.0mL of distilled/deionized water. Autoclave for 90 min at 15 psi pressure– 121°C. Allow to stand. Remove supernatant solution. Adjust pH to 6.6–6.8. Filter sterilize. Preparation of Medium: Add components, except fresh yeast extract solution and calf serum, to distilled/deionized water and bring volume to 550.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile fresh yeast extract solution and calf serum. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation and maintenance of Mycoplasma species.
Presumpto Media Composition per plate: Quadrant 1 ...................................................... 5.0mL Quadrant 2 ...................................................... 5.0mL
Proteose No. 3 Agar Quadrant 3....................................................... 5.0mL Quadrant 4....................................................... 5.0mL
Quadrant 1: Composition per 5.0mL: Lombard-Dowell agar..................................... 5.0mL
Quadrant 2: Composition per 5.0mL: Lombard-Dowell bile agar.............................. 5.0mL
Quadrant 3: Composition per 5.0mL: Lombard-Dowell egg yolk agar...................... 5.0mL
Quadrant 4: Composition per 5.0mL: Lombard-Dowell esculin agar ........................ 5.0mL
Preparation of Quadrant Media: Sterilize Lombard-Dowell Agar by autocalving for 15 min at 15 psi pressure–121°C. Cool to 45°-50°C. Add additional components as filter sterilized solutions. Mix and distribute as 5.0mL aliquots into quadrants. Use: For the differentiation and presumptive identification of anaerobic bacteria. The Presumpto media is a four-sectored plate each containing a different medium.
Proteose No. 3 Agar
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Preparation of Medium: Add components, except hemoglobin solution and supplement A, to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–60°C. Aseptically add 500.0mL of sterile hemoglobin solution and 10.0mL of sterile supplement A. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation and cultivation of Neisseria species, Hemophilus species, and other fastidious bacteria. For the cultivation and maintenance of Escherichia coli.
Proteose No. 3 Agar Composition per 1010.0mL: Proteose peptone no. 3......................................20.0g Agar ..................................................................15.0g Na2HPO4 .............................................................5.0g NaCl....................................................................5.0g Glucose ...............................................................0.5g Hemoglobin solution .................................. 500.0mL Supplement B................................................ 10.0mL pH 7.3 ± 0.2 at 25°C
Source: This medium is available as a premixed
Composition per 1010.0mL:
powder from BD Diagnostic Systems.
Proteose peptone no. 3 ......................................20.0g Agar ..................................................................15.0g Na2HPO4 .............................................................5.0g NaCl ....................................................................5.0g Glucose ...............................................................0.5g Hemoglobin solution................................... 500.0mL Supplement A ............................................... 10.0mL pH 7.3 ± 0.2 at 25°C
Hemoglobin Solution: Composition per 500.0mL:
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Supplement B: Composition per 10.0mL:
Hemoglobin Solution: Composition per 500.0mL:
Supplement B contains yeast concentrate, glutamine, coenzyme, cocarboxylase, hematin, and growth factors.
Hemoglobin ......................................................10.0g
Preparation of Hemoglobin Solution: Add hemoglobin to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Supplement A: Composition per 100.mL: Supplement A contains yeast concentrate with Crystal Violet.
Preparation of Supplement A: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Hemoglobin ......................................................10.0g
Preparation of Hemoglobin Solution: Add hemoglobin to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Preparation of Supplement B: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. Preparation of Medium: Add components, except hemoglobin solution and supplement B, to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–60°C. Aseptically add 500.0mL of sterile hemoglobin solution and 10.0mL of sterile supplement B. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
366
Proteose No. 3 Agar
Use: For the isolation and cultivation of Neisseria species, Hemophilus species, and other fastidious bacteria. For the cultivation and maintenance of Escherichia coli.
Proteose No. 3 Agar Composition per 1010.0mL: Proteose peptone no. 3 ......................................20.0g Agar ..................................................................15.0g Na2HPO4 .............................................................5.0g NaCl ....................................................................5.0g Glucose ...............................................................0.5g Hemoglobin solution................................... 500.0mL Supplement VX............................................. 10.0mL pH 7.3 ± 0.2 at 25°C
Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of a variety of bacteria.
Pseudomonas Agar F Composition per liter: Proteose peptone no. 3......................................20.0g Agar ..................................................................15.0g Glycerol ............................................................10.0g Pancreatic digest of casein................................10.0g K2HPO4...............................................................1.5g MgSO4·7H2O ....................................................0.73g pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Add components to
Hemoglobin Solution: Composition per 500.0mL:
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Hemoglobin ......................................................10.0g
Use: For the cultivation and observation of fluores-
Preparation of Hemoglobin Solution: Add he-
cein production in Pseudomonas species.
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
moglobin to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Supplement VX: Composition per 10.0mL: Supplement B contains essential growth factors.
Preparation of Supplement VX: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, ex-
Pseudomonas Agar F Composition per liter: Agar ..................................................................15.0g Glycerol ............................................................10.0g Proteose peptone no. 3......................................10.0g Pancreatic digest of casein................................10.0g K2HPO4...............................................................1.5g MgSO4·7H2O ......................................................1.5g pH 7.0 ± 0.2 at 25°C
cept hemoglobin solution and supplement VX, to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–60°C. Aseptically add 500.0mL of sterile hemoglobin solution and 10.0mL of sterile supplement VX. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Source: This medium is available as a premixed
Use: For the isolation and cultivation of Neisseria species, Hemophilus species, and other fastidious bacteria. For the cultivation and maintenance of Escherichia coli.
Use: For the isolation, cultivation, and differentia-
Proteose Yeast Extract Medium Composition per liter: Proteose peptone ...............................................20.0g Glucose .............................................................10.0g Yeast extract........................................................5.0g
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L.
powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes. tion of Pseudomonas aeruginosa on the basis of pigment production.
Pseudomonas Agar P Composition per liter: Proteose peptone no. 3......................................20.0g Agar ..................................................................15.0g Glycerol ............................................................10.0g K2HPO4.............................................................10.0g MgCl2·6H2O .......................................................1.4g pH 7.0 ± 0.2 at 25°C
Pseudomonas CN Agar Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the isolation, cultivation, and differentiation of Pseudomonas aeruginosa on the basis of pigment production.
Pseudomonas Basal Mineral Medium Composition per liter: K2HPO4 .............................................................12.5g KH2PO4 ...............................................................3.8g (NH4)2SO4...........................................................1.0g MgSO4·7H2O ......................................................0.1g Carbon source (0.8M solution) ................... 100.0mL Trace elements solution .................................. 5.0mL pH 7.2 ± 0.2 at 25°C
Trace ElementsSolution: Composition per liter: H3BO3 .............................................................0.232g ZnSO4·7H2O ...................................................0.174g FeSO4(NH4)2SO4·6H2O..................................0.116g CoSO4·7H2O ...................................................0.096g (NH4)6Mo7O24·4H2O ......................................0.022g CuSO4·5H2O ....................................................8.0mg MnSO4·4H2O ...................................................8.0mg
Preparation of Trace Elements Solution: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly.
Carbon Source: Composition per 100.0mL: Glucose .............................................................14.4g
Preparation of Carbon Source: Add glucose to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize. Other carbon sources may replace glucose. Prepare 0.8M carbon source solution.
Preparation of Medium: Add components, except carbon source, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 100.0mL of sterile carbon source. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
367
Use: For the cultivation and differentiation of Pseudomonas species based on their ability to grow on different carbon sources.
Pseudomonas CFC Agar Composition per liter: Pancreatic digest of gelatin...............................16.0g Agar .................................................................. 11.0g Pancreatic digest of casein................................10.0g K2SO4 ...............................................................10.0g MgCl2·6H2O .......................................................1.4g CFC selective supplement ............................ 10.0mL Glycerol ........................................................ 10.0mL pH 7.1 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath.
CFC Selective Supplement: Composition per 10.0mL: Cephaloridine....................................................0.05g Fucidin ..............................................................0.01g Cetrimide ..........................................................0.01g
Preparation of CFC Selective Supplement: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except CFC selective supplement, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile CFC selective supplement. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the selective isolation and cultivation of Pseudomonas species.
Pseudomonas CN Agar Composition per liter: Pancreatic digest of gelatin...............................16.0g Agar .................................................................. 11.0g Pancreatic digest of casein................................10.0g K2SO4 ...............................................................10.0g MgCl2·6H2O .......................................................1.4g CN selective supplement .............................. 10.0mL Glycerol ........................................................ 10.0mL
CN Selective Supplement: Cetrimide ............................................................0.1g Sodium nalidixate ............................................7.5mg pH 7.1 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath.
368
Purple Agar
Preparation of Medium: Add components, except CN selective supplement, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile CN selective supplement. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Bromcresol Purple ..........................................0.015g Carbohydrate solution................................... 20.0mL pH 6.8 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Carbohydrate Solution: Composition per 20.0mL:
Use: For the selective isolation and cultivation of
Carbohydrate.....................................................10.0g
Pseudomonas species.
Preparation of Carbohydrate Solution: Add
Purple Agar Composition per liter: Agar ..................................................................15.0g Proteose peptone no. 3 ......................................10.0g NaCl ....................................................................5.0g Beef extract .........................................................1.0g Bromcresol Purple ............................................0.02g Carbohydrate solution................................... 20.0mL pH 6.8 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Carbohydrate Solution: Composition per 20.0mL: Carbohydrate.....................................................10.0g
Preparation of Carbohydrate Solution: Add carbohydrate to distilled/deionized water and bring volume to 20.0mL. For expensive carbohydrates, 5.0g may be used instead of 10.0g. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except carbohydrate solution, to distilled/deionized water and bring volume to 980.0mL. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes in 9.8mL volumes. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 0.2mL of sterile carbohydrate solution to each tube. Mix thoroughly. Allow tubes to cool in a slanted position.
Use: For the preparation of carbohydrate media used in fermentation studies for the identification of bacteria, especially members of the Enterobacteriaceae. Bacteria that can ferment the carbohydrate turn the medium yellow.
Purple Broth (Purple Carbohydrate Broth) Composition per liter: Proteose peptone no. 3 ......................................10.0g NaCl ....................................................................5.0g Beef extract .........................................................1.0g
carbohydrate to distilled/deionized water and bring volume to 20.0mL. For expensive carbohydrates, 5.0g may be used instead of 10.0g. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except carbohydrate solution, to distilled/deionized water and bring volume to 980.0mL. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes in 9.8mL volumes. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C. Aseptically add 0.2mL of sterile carbohydrate solution to each tube. Mix thoroughly.
Use: For the preparation of carbohydrate media used in fermentation studies for the identification of bacteria, especially members of the Enterobacteriaceae. Bacteria that can ferment the carbohydrate turn the medium yellow.
Purple Broth Composition per liter: Pancreatic digest of gelatin...............................10.0g NaCl....................................................................5.0g Bromcresol Purple ............................................0.02g Carbohydrate solution................................... 20.0mL pH 6.8 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Carbohydrate Solution: Composition per 20.0mL: Carbohydrate.....................................................10.0g
Preparation of Carbohydrate Solution: Add carbohydrate to distilled/deionized water and bring volume to 20.0mL. For expensive carbohydrates, 5.0g may be used instead of 10.0g. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except carbohydrate solution, to distilled/deionized water and bring volume to 980.0mL. Mix thoroughly. Adjust pH to 7.4 if necessary. Distribute into tubes containing an inverted Durham tube. Fill each tube with 9.8mL of medium. Autoclave for 15 min at 15
PY Basal Medium psi pressure–121°C. Aseptically add 0.2mL of sterile carbohydrate solution to each tube.
Use: For the preparation of liquid fermentation media. Bacteria that can ferment the carbohydrate turn the medium yellow.
Purple Lactose Agar Composition per liter: Agar ..................................................................10.0g Lactose ..............................................................10.0g Peptone................................................................5.0g Beef extract .........................................................3.0g Bromcresol Purple ..........................................0.025g pH 6.8 ± 0.1 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes. Allow tubes to cool in a slanted position.
Use: For the detection and differentiation of members of the Enterobacteriaceae. Bacteria that can ferment lactose turn the medium yellow.
Purple Serum Agar Base Composition per liter: Agar ..................................................................20.0g Lactose ..............................................................20.0g Peptone..............................................................20.0g NaCl ....................................................................5.0g Bromcresol Purple ............................................0.03g Phenol Red......................................................0.024g pH 7.6 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and differentiation of Gramnegative bacteria isolated from the urinary tract. Bacteria that can ferment lactose turn the medium yellow.
PV Blood Agar (Paromomycin Vancomycin Blood Agar)
369
Pancreatic digest of casein................................15.0g NaCl....................................................................5.0g Papaic digest of soybean meal............................5.0g Yeast extract........................................................5.0g L-Cystine .............................................................0.4g Paromomycin......................................................0.1g Vancomycin .....................................................7.5mg Hemin ..............................................................5.0mg Sheep blood, defibrinated ............................. 50.0mL Vitamin K1 solution ...................................... 10.0mL pH 7.5 ± 0.2 at 25°C
Vitamin K1 Solution: Composition per 10.0mL: Vitamin K1 ........................................................0.01g Ethanol.......................................................... 10.0mL
Preparation of Vitamin K1 Solution: Add vitamin K1 to 10.0mL of absolute ethanol. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components—except vitamin K1 solution, sheep blood, paromomycin, and vancomycin—to distilled/deionized water and bring volume to 940.0mL. Mix thoroughly. Gently heat and bring to boiling for 1 min. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Aseptically add the sterile vitamin K1 solution, sheep blood, vancomycin, and paromomycin. Mix thoroughly. Pour into sterile Petri dishes.
Use: For the selective cultivation of fastidious anaerobic bacteria.
PY Basal Medium Composition per 104.0mL: Yeast extract........................................................1.0g L-Cysteine·HCl·H2O ...........................................0.5g Peptone ...............................................................0.5g Pancreatic digest of casein..................................0.5g Resazurin .......................................................0.16mg Salts solution................................................... 4.0mL
Salts Solution: Composition per liter: NaHCO3 ............................................................10.0g NaCl....................................................................2.0g K2HPO4...............................................................1.0g KH2PO4...............................................................1.0g CaCl2 ...................................................................0.2g MgSO4 ................................................................0.2g
Preparation of Salts Solution: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly.
Composition per liter:
Preparation of Medium: Add components to
Agar ..................................................................20.0g
distilled/deionized water and bring volume to
370
Pyrazinamidase Agar
104.0mL. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure– 121°C.
Use: For the identification of treponemes.
Bacteria that produce pyrazinamidase turn the medium pink.
Pyruvate Utilization Medium Composition per liter:
Pyrazinamidase Agar (Pyrazinamide Medium) Composition per liter: Pancreatic digest of casein................................15.0g Agar ..................................................................15.0g Papaic digest of soybean meal ............................5.0g NaCl ....................................................................5.0g Yeast extract........................................................3.0g Pyrazinecarboxamide..........................................1.0g Tris(hydroxymethyl)aminomethane maleate buffer (0.2M, pH 6.0)............................................. 1.0L pH 6.0 ± 0.2 at 25°C
Preparation of Medium: Combine components. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes in 5.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C. Allow tubes to cool in a slanted position.
Use: For the cultivation, differentiation, and maintenance of pathogenic Yersinia species. Bacteria that produce pyrazinamidase turn the medium pink.
Pyrazinamide Medium Composition per liter: Agar ..................................................................15.0g Na2HPO4 .............................................................2.5g Sodium pyruvate .................................................2.0g L-Asparagine .......................................................2.0g KH2PO4 ...............................................................1.0g Pancreatic digest of casein..................................0.5g Tween 80.............................................................0.2g Pyrazinamide ......................................................0.1g CaCl2·2H2O......................................................0.5mg CuSO4·5H2O ....................................................0.1mg ZnSO4·7H2O ....................................................0.1mg Ferric ammonium citrate...................................0.05g MgSO4·7H2O ....................................................0.01g pH 6.6 ± 0.2 at 25°C
Preparation of Medium: Combine components. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes in 5.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C. Allow tubes to cool in a slanted position.
Use: For the cultivation and differentiation of Corynebacterium species and related organisms.
Sodium pyruvate...............................................10.0g Pancreatic digest of casein................................10.0g K2HPO4...............................................................5.0g NaCl....................................................................5.0g Yeast extract........................................................5.0g Bromthymol Blue ...............................................0.1g pH 7.1–7.4 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Adjust pH to 7.1–7.4. Distribute into tubes in 5.0mL volumes. Autoclave for 15 min at 15 psi pressure– 121°C.
Use: For the cultivation of bacteria that can metabolize pyruvate. Bacteria that can utilize pyruvate turn the medium yellow.
Pyruvic Acid Egg Medium Composition per 1640.0mL: KH2PO4............................................................. 11.4g D-Glucose..........................................................10.0g Na2HPO4 .............................................................6.0g Pyruvic acid ........................................................3.0g MgSO4·7H2O ......................................................0.3g Malachite Green..............................................0.125g Egg, homogenized whole................................... 1.0L Penicillin solution ......................................... 10.0mL
Source: This medium is available as a prepared medium from Oxoid Unipath.
Penicillin Solution: Composition per 10.0mL: Penicillin G ................................................ 100,000U
Preparation of Penicillin Solution: Add penicillin G to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Homogenized Whole Egg: Composition per liter: Whole eggs ...................................................... 18-24
Preparation of Homogenized Whole Egg: Use fresh eggs, less than 1 week old. Scrub the shells with soap. Let stand in a soap solution for 30 min. Rinse in running water. Soak eggs in 70% ethanol for 15 min. Break the eggs into a sterile container. Homogenize by shaking. Filter through four layers of sterile cheesecloth into a sterile graduated cylinder.
Rabbit Serum Medium Preparation of Medium: Add components, except homogenized whole egg and penicillin solution, to distilled/deionized water and bring volume to 630.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 1.0L homogenized whole egg and penicillin solution to cooled sterile basal medium. Mix thoroughly. Aseptically distribute into sterile tubes. Inspissate at 85°–90°C (moist heat) for 45 min.
Use: For the isolation and cultivation of Mycobacterium species, especially ones that are drug resistant and difficult to grow.
R Medium Composition per liter: Agar ..................................................................30.0g NaHCO3 ..............................................................8.0g K2HPO4 ...............................................................3.0g Glucose ...............................................................2.5g Glutamine..........................................................0.61g Serine ................................................................0.24g Leucine..............................................................0.23g Lysine................................................................0.23g Asparagine ........................................................0.18g Valine ................................................................0.17g Isoleucine ..........................................................0.17g Tyrosine ............................................................0.14g Arginine·HCl...................................................0.125g Phenylalanine..................................................0.125g Threonine ..........................................................0.12g Methionine ......................................................0.073g Glycine............................................................0.065g Histidine·HCl ..................................................0.055g Proline.............................................................0.043g Tryptophan ......................................................0.035g L-Cystine .........................................................0.025g MgSO4·H2O .....................................................9.9mg CaCl2·2H2O......................................................7.4mg Adenine sulfate ................................................2.1mg Uracil ...............................................................1.4mg Thiamine·HCl ..................................................1.0mg MnSO4·H2O .....................................................0.9mg pH 8.0 ± 0.2 at 25°C
Preparation of Medium: Add components, except agar, to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Filter sterilize. Warm to 45°–50°C. Add agar to distilled/deionized water and bring volume to 500.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically combine both solutions. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation of Bacillus anthracis.
371
Rabbit Blood Agar Composition per 1250.0mL: Pancreatic digest of casein................................16.0g Agar ..................................................................13.5g Brain heart, solids from infusion ........................8.0g Peptic digest of animal tissue .............................5.0g NaCl....................................................................5.0g Na2HPO4 .............................................................2.5g Glucose ...............................................................2.0g Rabbit blood, defibrinated .......................... 250.0mL pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components, except rabbit blood, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Autoclave for 15 min at 15 psi–121°C. Aseptically add sterile rabbit blood. Pour into sterile Petri dishes or aseptically distribute into sterile tubes or flasks while shaking.
Use: For the cultivation and maintenance of Corynebacterium diphtheriae, Haemophilus ducreyi, and Actinobacillus lignieresii.
Rabbit Heart Infusion Agar Composition per liter: Beef heart, infusion from................................500.0g Agar ..................................................................15.0g Tryptose ............................................................10.0g NaCl....................................................................5.0g Rabbit blood, defibrinated ............................ 50.0mL pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components, except rabbit blood, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Aseptically add 50.0mL of sterile rabbit blood. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the culture of Bartonella quintana.
Rabbit Serum Medium (Rabbit Serum Bovine Serum Albumin Tween 80 Medium) (Rabbit Serum BSA Tween 80 Medium) Composition per liter: Basal medium ............................................. 900.0mL Rabbit serum with supplements.................. 100.0mL pH 7.4 ± 0.2 at 25°C
Basal Medium: Composition per 900.0mL: Na2HPO4 .............................................................1.0g NaCl....................................................................1.0g KH2PO4...............................................................0.3g
372
Rainbow Agar O157
Rabbit serum ............................................... 100.0mL L-Asparagine (3% solution) ............................ 5.0mL MgCl2-CaCl2 solution..................................... 1.0mL
specific for two E. coli-associated enzymes: β-galactosidase (a blue-black chromogenic substrate) and βglucuronidase (a red chromogenic substrate). The distinctive black or gray coloration of E. coli O157:H7 colonies is easily viewed by laying the Petri plate against a white background. When O157 is surrounded by pink or magenta non-toxigenic colonies, it may have a bluish hue. The addition of selective agents improves performance. E. coli O157:H7 colony coloration will be slightly bluer with these selective agents added.Tellurite is highly selective for E. coli O157:H7 and can reduce background flora considerably. Novobiocin inhibits Proteus swarming and the growth of tellurite-reducing bacteria. Rare strains of O157:H7 are tellurite sensitive5.
Preparation of Rabbit Serum with Supplements: Combine the three solutions. Mix thorough-
RAMBACH® Agar
Glycerol (10% solution).................................. 1.0mL NH4Cl (25% solution)..................................... 1.0mL Sodium pyruvate (10% solution) .................... 1.0mL Thiamine (0.5% solution) ............................... 1.0mL
Preparation of Basal Medium: Add components to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 20 min at 15 psi pressure– 121°C. Cool to 25°C.
Rabbit Serum with Supplements: Composition per 106.0mL:
ly. Filter sterilize.
Composition per liter:
MgCl2-CaCl2 Solution: Composition per 100.0mL:
Preparation of MgCl2-CaCl2 Solution: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly.
NaC ....................................................................l5.0g Agar ..................................................................15.0g Proplylene glycol ..............................................10.5g Peptone ...............................................................8.0g Chromogenic mix ...............................................1.5g Sodium deoxycholate..........................................1.0g pH 7.3 ± 0.2 at 25°C
Preparation of Medium: Aseptically combine
Source: This medium is available from Merck.
CaCl2·2H2O.........................................................1.5g MgCl2·6H2O .......................................................1.5g
900.0mL of cooled sterile basal medium and 100.0mL of sterile rabbit serum with supplements. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation of Leptospira species.
Rainbow Agar O157 Composition per liter: Proprietary.
Source: This medium is available as a premixed powder from Biolog Inc. Preparation: Suspend 60.0g of the proprietary mixture in distilled/deionized water and bring volume to 1.0L Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45-50°C. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes. The final medium should be clear and virtually colorless. No pH adjustment is needed. The final pH should be pH 7.9-8.3. To increase the selectivity of the medium, a sterile solution containing 0.8 mg potassium tellurite and 10 mg novobiocin can be added. Caution must be used because tellurite is toxic.
Use: For the detection, isolation, and presumptive identification of verotoxin-producing strains of Escherichia coli, particularly serotype O157:H7. The medium contains chromogenic substrates that are
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Heat in a boiling water-batch or in a current of steam, while shaking from time to time. The medium is totally suspended, if no visual particles stick to the glass-wall. The medium should not be heat-treated further. Complete dissolution with shaking in 5-min. sequences is approximately 35-40 min. Do not autoclave. Do not overheat. Cool as fast as possible to 45°–50°C while gently shaking from time to time. Pour into sterile Petri dishes. To prevent any precipitate or clotting of the chromogenic-mix in the plates, place Petri dishes during pouring procedure on a cool (max. 25°C) surface. The plates are opaque and pink.
Use: For the detection of enteric bacteria, including coliforms and Salmonella spp. Sodium desoxycholate inhibits the accompanying Gram-positive flora. This medium enables Salmonella spp. to be differentiated unambiguously from other bacteria. Salmonella spp. form a characteristic red color. In order to differentiate coliforms from Salmonellae, the medium contains a chromogene indicating the presence of βgalactosidase splitting, a characteristic for coliforms. Coliform microorganisms grow as blue-green or blue-violet colonies. Other Enterobacteriaceae and Gram-negative bacteria, such as Proteus, Pseudomo-
Rappaport Broth, Modified nas, Shigella, S. typhi and S. parathyphi A grow as colorless-yellow colonies.
Rapid Fermentation Medium Composition per liter: Pancreatic digest of casein................................20.0g NaCl ....................................................................5.0g Agar ....................................................................3.5g L-Cystine .............................................................0.5g Na2SO3 ................................................................0.5g Phenol Red......................................................0.017g pH 7.3 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the differentiation of Neisseria species isolated from clinical specimens.
RAPID´E. coli 2 Agar Composition per liter: Proprietary
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D-Xylose ...........................................................10.0g
LiCl .....................................................................9.0g Meat extract ........................................................5.0g Yeast extract........................................................1.0g Phenol Red........................................................0.12g Selective supplement, proprietary ....................20.0g Chromogenic substrate, proprietary................ 1.0mL pH 7.3 ± 0.1 at 25°C
Source: This medium is available from Biorad. Use: For the detection and differentiation of Listeria spp., including L. ivanovii and L. monocytogenes.
Rappaport Broth, Modified (Rap Broth, Modified) Composition per 250.2mL: Solution A................................................... 155.0mL Solution C ..................................................... 53.0mL Solution B ..................................................... 40.0mL Solution D....................................................... 1.6mL Solution E ....................................................... 0.6mL
Solution A: Composition per liter: Pancreatic digest of casein................................10.0g
Source: This medium is available from Biorad.
Preparation of Solution A: Add pancreatic di-
Use: For the direct enumeration of E.coli and
gest of casein to distilled/deionized water and bring volume to 1.0L. Mix thoroughly.
coliforms. Selectivity and electivity are based on the detection of glucuronidase and galactosidase activities. Hydrolysis of chromogenic substrate results in purple to pink E.coli colonies (gluc+/gal+) and bluegreen coliform colonies (gluc-/gal+). RAPID´E.coli 2 agar is AFNOR validated according to ISO 16140 protocol to enumerate E.coli and coliforms on the same plate at 37°C, without any further confirmation of characteristic colonies.
RAPID´Enterococcus Agar
Solution B: Composition per liter: Na2HPO4 .............................................................9.5g
Preparation of Solution B: Add Na2HPO4 to dis-
tilled/deionized water and bring volume to 1.0L. Mix thoroughly.
Solution C: Composition per 100.0mL:
Composition per liter:
MgCl2·6H2O .....................................................40.0g
Proprietary
Preparation of Solution C: Add MgCl2·6H2O to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C.
Source: This medium is available from Biorad. Use: For the direct enumeration, without confirmation, of enterococci. The cleavage of the chromogenic substrate by glucosidase activity of Enterococci leads to specific blue colonies. RAPID´Enterococcus totally inhibits growth of Gram-negative flora and that of practically all Gram-positive bacteria other than Enterococci, due to the combined action of temperature and selective media.
RAPID´L. mono Medium Composition per liter: Peptones ............................................................30.0g Agar B, proprietary ...........................................13.0g
Solution D: Composition per 100.0mL: Malachite Green..................................................0.2g
Preparation of Solution D: Add Malachite Green to sterile distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Do not sterilize. Solution E: Composition per 10.0mL: Carbenicillin .....................................................0.01g
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Rappaport-Vassiliadis Enrichment Broth
Preparation of Solution E: Add carbenicillin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Combine 155.0mL of solution A and 40.0mL of solution B. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 53.0mL of sterile solution C, 1.6mL of solution D, and 0.6mL of sterile solution E. Mix thoroughly. Aseptically distribute into sterile tubes or flasks. Use: For the isolation and cultivation of Yersinia enterocolitica.
Papaic digest of soybean meal..........................4.54g KH2PO4.............................................................1.45g Malachite Green oxalate .................................0.036g pH 5.1 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into screw-capped tubes in 10.0mL volumes. Autoclave for 15 min at 10 psi pressure–116°C.
Use: For the isolation and cultivation of Salmonella species.
Rappaport-Vassiliadis Enrichment Broth (RV Enrichment Broth) Composition per 1110.0mL: NaCl ....................................................................8.0g Papaic digest of soybean meal ............................5.0g KH2PO4 ...............................................................1.6g Magnesium chloride solution...................... 100.0mL Malachite Green solution.............................. 10.0mL pH 5.2 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath. Magnesium Chloride Solution: Composition per 100.0mL: MgCl2·6H2O .....................................................40.0g
Preparation of Magnesium Chloride Solution: Add MgCl2·6H2O to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Rappaport-Vassiliadis Soya Peptone Broth (RVS Broth) Composition per liter: MgCl2, anhydrous...........................................13.58g NaCl....................................................................7.2g Papaic digest of soybean meal............................4.5g KH2PO4.............................................................1.26g K2HPO4.............................................................0.18g Malachite Green..............................................0.036g pH 5.2 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into screw-capped tubes in 10.0mL volumes. Autoclave for 15 min at 10 psi pressure–115°C.
Use: For the isolation and cultivation of Salmonella
Malachite Green Solution: Composition per 10.0mL:
species.
Malachite Green oxalate ...................................0.04g
Reactivation with Tryptone Soya Broth (DSMZ Medium 220a)
Preparation of Malachite Green Solution: Add Malachite Green to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes in 10.0mL volumes. Autoclave for 15 min at 10 psi pressure–115°C.
Use: For the isolation and cultivation of Salmonella species.
Rappaport-Vassiliadis R10 Broth Composition per liter: MgCl2, anhydrous .............................................13.4g NaCl ....................................................................7.2g
Composition per liter: Peptone from casein..........................................17.0g Peptone from soymeal ........................................3.0g NaCl....................................................................5.0g D(+)-Glucose.......................................................2.5g K2HPO4...............................................................2.5g pH 7.3 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the reactivation and cultivation of Aeromonas spp. and Burkholderia spp.
Regan-Lowe Semisolid Transport Medium
Reduced Transport Fluid Composition per liter: (NH4)2SO4...........................................................9.0g NaCl ....................................................................9.0g K2HPO4 ...............................................................4.5g KH2PO4 ...............................................................4.5g Na2CO3 ...............................................................4.0g EDTA (ethylenediamine tetraacetic acid)...........3.8g Dithiothreitol.......................................................2.0g MgSO4·7H2O ......................................................1.8g pH 8.0 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize. Aseptically distribute into sterile tubes with rubber stoppers.
Use: For the transport and isolation of bacteria from dental plaque, especially Streptococcus mutans and Streptococcus sanguis. Also used for the cultivation of a variety of Gram-positive bacteria from the oral cavity, especially streptococci, actinomycetes, lactobacilli, clostridia, Bacteroides species, Fusobacterium species, and Veillonella species.
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Use: For the transport and isolation of bacteria from dental plaque, especially Streptococcus mutans and Streptococcus sanguis. Also used for the cultivation of a variety of Gram-positive bacteria from the oral cavity, especially streptococci, actinomycetes, lactobacilli, clostrida, Bacteroides, Fusobacteria, and Veillonela.
Regan-Lowe Charcoal Agar (Regan-Lowe Medium) Composition per liter: Agar ..................................................................12.0g Beef extract.......................................................10.0g Pancreatic digest of gelatin...............................10.0g Soluble starch....................................................10.0g NaCl....................................................................5.0g Charcoal..............................................................4.0g Niacin................................................................0.01g Horse blood, defibrinated ........................... 100.0mL Cephalexin solution ...................................... 10.0mL pH 7.4 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Reduced Transport Fluid Composition per liter: Stock mineral salt solution no. 1................... 75.0mL Stock mineral salt solution no. 2................... 75.0mL Dithiothreitol (1% solution).......................... 20.0mL Ethylenediamine tetraacetic acid (1M solution) .......................................... 10.0mL Na2CO3 (8% solution).................................... 5.0mL Resazurin (0.1% solution)............................... 1.0mL pH 8.0 ± 0.2 at 25°C
Stock Mineral Salt Solution No. 1: Composition per 100.0mL: K2HPO4 ...............................................................0.6g
Preparation of Stock Mineral Salt Solution No. 1: Add K2HPO4 to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly.
Stock Mineral Salt Solution No. 2: Composition per 100.0mL: NaCl ....................................................................1.2g (NH4)2SO4...........................................................1.2g K2HPO4 ...............................................................0.6g MgSO4·7H2O ....................................................0.25g
Preparation of Stock Mineral Salt Solution No. 2: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize. Aseptically distribute into sterile tubes with rubber stoppers.
Cephalexin Solution: Composition per 10.0mL: Cephalexin ........................................................0.04g
Preparation of Cephalexin Solution: Add cephalexin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except horse blood and cephalexin solution, to distilled/ deionized water and bring volume to 890.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile horse blood and sterile cephalexin solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes. Swirl medium while dispensing to keep charcoal in suspension.
Use: For the selective isolation and cultivation of Bordetella pertussis and Bordetella parapertussis from clinical specimens.
Regan-Lowe Semisolid Transport Medium Composition per liter: Agar ....................................................................6.0g Beef extract.........................................................5.0g Pancreatic digest of gelatin.................................5.0g Soluble starch......................................................5.0g NaCl....................................................................2.5g Charcoal..............................................................2.0g
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Reinforced Clostridial Agar
Niacin................................................................0.01g Horse blood, defibrinated ........................... 100.0mL Cephalexin solution ...................................... 10.0mL pH 7.4 ± 0.2 at 25°C
Cephalexin Solution: Composition per 10.0mL: Cephalexin ........................................................0.04g
Preparation of Cephalexin Solution: Add cephalexin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. Preparation of Medium: Add components, except horse blood and cephalexin solution, to distilled/ deionized water and bring volume to 890.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile horse blood and sterile cephalexin solution. Mix thoroughly. Aseptically distribute into small, sterile, screw-capped tubes. Fill tubes half-full. Swirl medium while dispensing to keep charcoal in suspension.
Use: For the transport of Bordetella pertussis and Bordetella parapertussis isolated from clinical specimens.
Reinforced Clostridial Agar Composition per liter: Agar ..................................................................13.5g Beef extract .......................................................10.0g Pancreatic digest of casein................................10.0g NaCl ....................................................................5.0g Glucose ...............................................................5.0g Yeast extract........................................................3.0g Sodium acetate....................................................3.0g Soluble starch......................................................1.0g L-Cysteine·HCl·H2O............................................0.5g pH 6.8 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems and Oxoid Unipath. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 10 psi pressure–115°C. Pour into sterile Petri dishes or leave in tubes.
Beef extract.......................................................10.0g Glucose ...............................................................5.0g NaCl....................................................................5.0g Yeast extract........................................................3.0g Sodium acetate....................................................3.0g Soluble starch......................................................1.0g L-Cysteine·HCl·H2O ...........................................0.5g Agar ....................................................................0.5g pH 6.8 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems and Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 10 psi pressure–115°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the nonselective cultivation and enumeration of Clostridium species, other anaerobes such as lactobacilli, and facultative organisms from clinical specimens.
Reinforced Clostridial Medium with Sodium Lactate Composition per liter: Tryptose ............................................................10.0g Beef extract.......................................................10.0g Glucose ...............................................................5.0g NaCl....................................................................5.0g Yeast extract........................................................3.0g Sodium acetate....................................................3.0g Soluble starch......................................................1.0g L-Cysteine·HCl·H2O ...........................................0.5g Agar ....................................................................0.5g Sodium lactate (60% solution)...................... 15.0mL pH 6.8 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 10 psi pressure–115°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the nonselective cultivation and enumera-
Use: For the cultivation and enumeration of
tion of Clostridium species, other anaerobes such as lactobacilli, from clinical specimens.
Clostridium species, Bifidobacterium species, other anaerobes (e.g., lactobacilli), and facultative organisms from clinical specimens.
Composition per liter:
Reinforced Clostridial Medium Composition per liter: Tryptose ............................................................10.0g
Rice Extract Agar Agar ..................................................................20.0g White rice, solids from extract............................5.0g Polysorbate 80 .............................................. 10.0mL pH 6.6 ± 0.2 at 25°C
Rogosa Agar Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components, except polysorbate 80, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Add polysorbate 80. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes.
Use: For the cultivation and differentiation of Candida albicans and Candida stellatoidea from other Candida species based on chlamydospore formation.
Rice Extract Agar Composition per liter: Agar ..................................................................20.0g White rice, solids from extract..........................20.0g pH 7.1 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components, ex-
Preparation of Novobiocin Solution: Add novobiocin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except novobiocin solution, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile components. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the selective isolation, cultivation, and presumptive identification of Aeromonas hydrophila and other Gram-negative bacteria based on their ability to decarboxylate lysine and ornithine, ferment maltose, and produce H2S. Maltose-fermenting bacteria appear as yellow colonies. Bacteria that produce lysine or ornithine decarboxylase turn the medium greenish-yellow to yellow. Bacteria that produce H2S appear as colonies with black centers.
RIOT Agar (Rice Infusion Oxgall Tween 80 Agar)
cept polysorbate 80, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Add polysorbate 80. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes.
Composition per 1010.0mL:
Use: For the cultivation and differentiation of Can-
Rice Extract: Composition per liter:
dida albicans and Candida stellatoidea from other Candida species based on chlamydospore formation.
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Agar ..................................................................10.0g Oxgall ...............................................................10.0g Rice extract ........................................................ 1.0L Tween 80....................................................... 10.0mL pH 7.3 ± 0.2 at 25°C
Cream of rice cereal..........................................10.0g
Preparation of Rice Extract: Add cream of rice
Rimler-Shotts Medium (RS Medium) Composition per liter: Agar ..................................................................13.5g Na2S2O3·5H2O ....................................................6.8g L-Ornithine·HCl ..................................................6.5g NaCl ....................................................................5.0g L-Lysine·HCl .......................................................5.0g Maltose................................................................3.5g Yeast extract........................................................3.0g Sodium deoxycholate..........................................1.0g Ferric ammonium citrate.....................................0.8g L-Cysteine·HCl....................................................0.3g Bromthymol Blue .............................................0.03g Novobiocin solution...................................... 10.0mL pH 7.0 ± 0.2 at 25°C
Novobiocin Solution: Composition per 10.0mL: Novobiocin.......................................................5.0mg
cereal to 1.0L of boiling tap water. Mix thoroughly. Filter quickly through cheesecloth. Bring volume of filtrate to 1.0L with tap water.
Preparation of Medium: Combine components. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and differentiation of Candida albicans and Candida stellatoidea from other Candida species based on chlamydospore formation.
Rogosa Agar Composition per liter: Sodium acetate..................................................25.0g Agar ..................................................................20.0g Glucose .............................................................20.0g Pancreatic digest of casein................................10.0g KH2PO4...............................................................6.0g Yeast extract........................................................5.0g
378
Rogosa SL Agar
Ammonium citrate ..............................................2.0g Sorbitan monooleate ...........................................1.0g MgSO4·7H2O ..................................................0.575g MnSO4·H2O ......................................................0.12g FeSO4·7H2O.....................................................0.4mg Acetic acid, glacial........................................ 1.32mL pH 5.4 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath. Preparation of Medium: Add components, except acetic acid, to distilled/deionized water and bring volume to 998.7mL. Mix thoroughly. Gently heat and bring to boiling. Add glacial acetic acid. Mix thoroughly. Gently heat while stirring and bring to 90°–100°C for 2–3 min. Do not autoclave. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation, cultivation, and enumeration of lactobacilli, especially from feces, saliva, and vaginal specimens.
Rogosa SL Agar (Rogosa Selective Lactobacillus Agar) Composition per liter: Agar ..................................................................15.0g Sodium acetate..................................................15.0g Glucose .............................................................10.0g Pancreatic digest of casein................................10.0g K2HPO4 ...............................................................6.0g Yeast extract........................................................5.0g Arabinose ............................................................5.0g Sucrose................................................................5.0g Ammonium citrate ..............................................2.0g Sorbitan monooleate ...........................................1.0g MgSO4·7H2O ....................................................0.57g MnSO4·7H2O ....................................................0.12g FeSO4·H2O........................................................0.03g Acetic acid, glacial........................................ 1.32mL pH 5.4 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components, except glacial acetic acid, to distilled/deionized water and bring volume to 998.7mL. Mix thoroughly. Gently heat and bring to boiling. Add glacial acetic acid. Mix thoroughly. Gently heat while stirring and bring to 90°–100°C for 2–3 min. Do not autoclave. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation, cultivation, and enumeration of lactobacilli, especially from feces, saliva, and vaginal specimens.
Rogosa SL Broth (Rogosa Selective Lactobacillus Broth) Composition per liter: Sodium acetate..................................................15.0g Glucose .............................................................10.0g Pancreatic digest of casein................................10.0g K2HPO4...............................................................6.0g Yeast extract........................................................5.0g Arabinose............................................................5.0g Sucrose................................................................5.0g Ammonium citrate ..............................................2.0g Sorbitan monooleate ...........................................1.0g MgSO4·7H2O ....................................................0.57g MnSO4·7H2O ....................................................0.12g FeSO4·H2O........................................................0.03g Acetic acid, glacial........................................ 1.32mL pH 5.4 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components, except glacial acetic acid, to distilled/deionized water and bring volume to 998.7mL. Mix thoroughly. Gently heat and bring to boiling. Add glacial acetic acid. Mix thoroughly. Gently heat while stirring and bring to 90°–100°C for 2–3 min. Do not autoclave. Aseptically distribute into sterile tubes.
Use: For the isolation, cultivation, and enumeration of lactobacilli, especially from feces, saliva, and vaginal specimens.
RPMI 1640 Medium with L-Glutamine Composition per liter: NaCl....................................................................6.0g NaHCO3 ..............................................................2.0g D-Glucose ............................................................2.0g Na2HPO4·7H2O...................................................1.5g KCl......................................................................0.4g L-Glutamine ........................................................0.3g L-Arginine ...........................................................0.2g Ca(NO3)2·4H2O ...................................................0.1g MgSO4·7H2O ......................................................0.1g L-Asparagine .....................................................0.05g L-Cystine ...........................................................0.05g L-Isoleucine, allo free........................................0.05g L-Leucine, methionine free ...............................0.05g L-Lysine·HCl .....................................................0.04g i-Inositol..........................................................0.035g L-Serine .............................................................0.03g L-Aspartic acid ..................................................0.02g L-Glutamic acid.................................................0.02g L-Hydroxyproline..............................................0.02g L-Proline, hydroxy-L-proline free......................0.02g L-Threonine, allo free........................................0.02g
SABHI Agar L-Tyrosine..........................................................0.02g L-Valine .............................................................0.02g L-Histidine,
free base.......................................0.015g
L-Methionine ...................................................0.015g L-Phenylalanine...............................................0.015g
Glycine..............................................................0.01g L-Tryptophan ....................................................5.0mg Phenol Red.......................................................5.0mg Choline chloride...............................................3.0mg Glutathione, reduced........................................1.0mg p-Aminobenzoic acid.......................................1.0mg Folic acid..........................................................1.0mg Nicotinamide....................................................1.0mg Pyridoxine·HCl ................................................1.0mg Thiamine·HCl ..................................................1.0mg D-Calcium pantothenate .................................0.25mg Biotin ...............................................................0.2mg Riboflavin ........................................................0.2mg Vitamin B12 ...................................................... 5.0µg pH 7.3 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Adjust pH to 7.3 with 1N HCl or 1N NaOH. Filter sterilize. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation of mammalian cells in tissue culture. Culture media for human immunodeficiency viruses.
Russell Double-Sugar Agar Composition per liter: Agar ..................................................................15.0g Proteose peptone no. 3 ......................................12.0g Lactose ..............................................................10.0g NaCl ....................................................................5.0g Beef extract .........................................................1.0g Glucose ...............................................................1.0g Phenol Red......................................................0.025g pH 7.5 ± 0.2 at 25°C
Preparation of Medium: Add components to dis-
379
SABHI Agar (Sabouraud Glucose and Brain Heart Infusion Agar) Composition per liter: Glucose .............................................................21.0g Agar ..................................................................15.0g Pancreatic digest of casein................................10.5g Peptic digest of animal tissue .............................5.0g Brain heart, solids from infusion ........................4.0g NaCl....................................................................2.5g Na2HPO4 ...........................................................1.25g pH 6.8 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes in 20.0mL volumes or leave in tubes.
Use: For the cultivation of dermatophytes and other pathogenic and nonpathogenic fungi from clinical and nonclinical specimens.
SABHI Agar Composition per liter: Beef heart, infusion from................................125.0g Calf brains, infusion from...............................100.0g Glucose .............................................................21.0g Agar ..................................................................15.0g Neopeptone .........................................................5.0g Proteose peptone.................................................5.0g NaCl....................................................................2.5g Na2HPO4 ...........................................................1.25g Chloromycetin solution .................................. 1.0mL pH 7.0 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Chloromycetin Solution: Composition per 10.0mL:
tilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes. Autoclave for 15 min at 15 psi pressure– 121°C. Allow tubes to cool in a slanted position.
Chloromycetin ....................................................1.0g
Use: For the identification of Gram-negative enteric
Preparation of Medium: Add components, ex-
bacilli based on their fermentation of glucose and lactose. Bacteria that ferment both glucose and lactose produce a yellow slant and yellow butt. Bacteria that ferment glucose but do not ferment lactose produce a red slant and a yellow butt. Bacteria that ferment neither glucose nor lactose produce an unchanged pink-orange color.
cept chloromycetin solution, to distilled/deionized water and bring volume to 999.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 1.0mL of sterile chloromycetin solution. Mix thoroughly. Aseptically distribute into sterile tubes in 5.0mL volumes.
Preparation of Chloromycetin Solution: Add chloromycetin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
380
SABHI Agar, Modified
Use: For the cultivation of dermatophytes and other pathogenic and nonpathogenic fungi from clinical and nonclinical specimens.
SABHI Agar, Modified Composition per liter: Beef heart, infusion from ..................................62.5g Calf brain, infusion from ..................................50.0g Glucose .............................................................20.5g Brain heart infusion broth .................................18.6g Agar ....................................................................7.5g Neopeptone .........................................................5.0g Pancreatic digest of gelatin .................................2.5g NaCl ..................................................................1.25g Na2HPO4 .........................................................0.625g pH 6.8 ± 0.2 at 25°C
Preparation of Medium: Dissolve, then autoclave at 15 psi pressure–121°C for 15 min. Cool to 50°C and add 1.0mL of sterile chloramphenicol solution (100.0mg/mL). Mix well and dispense into sterile tubes. Slant and allow to harden. Refrigerate until needed.
Use: For the cultivation of dermatophytes and other pathogenic and nonpathogenic fungi from clinical and nonclinical specimens.
SABHI Blood Agar Composition per liter: Beef heart, infusion from ................................125.0g Calf brains, infusion from...............................100.0g Glucose .............................................................21.0g Agar ..................................................................15.0g Neopeptone .........................................................5.0g Proteose peptone .................................................5.0g NaCl ....................................................................2.5g Na2HPO4 ...........................................................1.25g Blood........................................................... 100.0mL Chloromycetin solution................................... 1.0mL pH 7.0 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Chloromycetin Solution: Composition per 10.0mL: Chloromycetin ....................................................1.0g
Preparation of Chloromycetin Solution: Add chloromycetin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except blood and chloromycetin solution, to distilled/deionized water and bring volume to 899.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 100.0mL of sterile blood and 1.0mL of sterile
chloromycetin solution. Sheep blood or human blood may be used. Mix thoroughly. Aseptically distribute into sterile tubes in 5.0mL volumes.
Use: For the cultivation of dermatophytes and other pathogenic and nonpathogenic fungi from clinical and nonclinical specimens. Blood enhances the recovery of Blastomyces dermatitidis and Histoplasma capsulatum and their conversion to the yeast phase.
Sabouraud Agar Composition per liter: Neopeptone .......................................................30.0g Agar ..................................................................20.0g
Preparation of Medium: Add components to tap water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure– 121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation of yeasts and molds.
Sabouraud Agar with CCG and 3% NaCl Composition per 3031.5mL: Glucose ...........................................................120.0g NaCl..................................................................90.0g Agar ..................................................................45.0g Peptone .............................................................30.0g Chloramphenicol solution............................. 15.0mL Cycloheximide solution ................................ 15.0mL Gentamicin solution........................................ 1.5mL
Chloramphenicol Solution: Composition per 15.0mL: Chloramphenicol...............................................0.15g
Preparation of Chloramphenicol Solution: Add chloramphenicol to distilled/deionized water and bring volume to 15.0mL. Mix thoroughly. Filter sterilize.
Cycloheximide Solution: Composition per 15.0mL: Cycloheximide....................................................0.3g
Preparation of Cycloheximide Solution: Add cycloheximide to distilled/deionized water and bring volume to 15.0mL. Mix thoroughly. Filter sterilize. Gentamicin Solution: Composition per 10.0mL: Gentamicin..........................................................0.4g
Preparation of Gentamicin Solution: Add gentamicin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Sabouraud Maltose Agar Preparation of Medium: Add components—except chloramphenicol solution, cycloheximide solution, and gentamicin solution—to distilled/deionized water and bring volume to 3.0L. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 15.0mL of sterile chloramphenicol solution, 15.0mL of sterile cycloheximide solution, and 1.5mL of sterile gentamicin solution. Mix thoroughly. Aseptically distribute into sterile tubes. Allow tubes to cool in a slanted position.
Use: For the selective isolation and cultivation of fungi from specimens with a mixed flora.
Sabouraud Agar with CCG and 5% NaCl Composition per 3031.5mL: NaCl ................................................................150.0g Glucose ...........................................................120.0g Agar ..................................................................45.0g Peptone..............................................................30.0g Chloramphenicol solution............................. 15.0mL Cycloheximide solution ................................ 15.0mL Gentamicin solution........................................ 1.5mL
Chloramphenicol Solution: Composition per 15.0mL:
381
oughly. Aseptically distribute into sterile tubes. Allow tubes to cool in a slanted position.
Use: For the selective isolation and cultivation of fungi from specimens with a mixed flora.
Sabouraud Glucose Agar, Emmons Composition per liter: Glucose .............................................................20.0g Agar ..................................................................17.0g Pancreatic digest of casein..................................5.0g Peptic digest of animal tissue .............................5.0g pH 6.9 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 13 psi pressure–118°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation of dermatophytes and other pathogenic and nonpathogenic fungi from clinical and nonclinical specimens. For the cultivation of yeast and filamentous fungi.
Chloramphenicol...............................................0.15g
Preparation of Chloramphenicol Solution: Add chloramphenicol to distilled/deionized water and bring volume to 15.0mL. Mix thoroughly. Filter sterilize.
Cycloheximide Solution: Composition per 15.0mL: Cycloheximide ....................................................0.3g
Preparation of Cycloheximide Solution: Add cycloheximide to distilled/deionized water and bring volume to 15.0mL. Mix thoroughly. Filter sterilize.
Gentamicin Solution: Composition per 10.0mL: Gentamicin..........................................................0.4g
Preparation of Gentamicin Solution: Add gentamicin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Sabouraud Glucose Broth Composition per liter: Glucose .............................................................20.0g Neopeptone .......................................................10.0g pH 5.6 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Avoid overheating.
Use: For the cultivation of pathogenic and nonpathogenic fungi, especially dermatophytes. The medium may be made more selective for fungi by the addition of chloramphenicol.
Preparation of Medium: Add components—except chloramphenicol solution, cycloheximide solution, and gentamicin solution—to distilled/deionized water and bring volume to 3.0L. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 15.0mL of sterile chloramphenicol solution, 15.0mL of sterile cycloheximide solution, and 1.5mL of sterile gentamicin solution. Mix thor-
Sabouraud Maltose Agar Composition per liter: Maltose .............................................................40.0g Agar ..................................................................15.0g Pancreatic digest of casein..................................5.0g Peptic digest of animal tissue .............................5.0g pH 5.6 ± 0.2 at 25°C
382
Sabouraud Maltose Broth
Source: This medium is available as a premixed powder from BD Diagnostic Systems and Oxoid Unipath.
Meat extract ........................................................1.0g Sodium deoxycholate..........................................1.0g pH 7.3 ± 0.2 at 25°C
Preparation of Medium: Add components to
Source: This medium is available from Fluka, Sig-
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Avoid overheating. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of a variety of fungi.
Sabouraud Maltose Broth Composition per liter: Maltose..............................................................40.0g Neopeptone .......................................................10.0g pH 5.6 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Avoid overheating.
Use: For the cultivation of a variety of fungi.
Sabouraud Medium, Fluid Composition per liter: Glucose .............................................................20.0g Pancreatic digest of casein..................................5.0g Peptamin .............................................................5.0g pH 5.7 ± 0.2at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems and Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Avoid overheating.
Use: For the isolation and cultivation of yeasts and molds.
Salmonella Chromogen Agar (Rambach Equivalent Agar) Composition per liter: Agar ..................................................................15.0g Peptone................................................................5.0g NaCl ....................................................................5.0g Yeast extract........................................................2.0g
ma-Aldrich.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Pour into sterile Petri dishes.
Use: For the detection of Salmonella spp.
Salmonella Chromogenic Agar Composition per liter: Chromogenic mix .............................................28.0g Agar ..................................................................12.0g Special peptone.................................................10.0g Selective supplement solution ...................... 10.0mL pH 7.2 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath.
Selective Supplement Solution: Composition per 10.0mL: Cefsulodin......................................................12.0mg Novobiocin ......................................................5.0mg
Preparation of Selective Supplement Solution: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0mL Mix thoroughly. Gently heat while stirring and bring to boiling. Do not autoclave. Cool quickly to 50°C. Mix thoroughly. Pour into sterile Petri dishes.
Use: For the identification of Salmonella species and differentiation of Salmonella spp. other organisms in the family Enterobacteriaceae. This medium combines two chromogens for the detection of Salmonella spp., 5-bromo-6-chloro-3-indolyl caprylate (Magenta-caprylate) and 5-bromo-4-chloro-3-Indolyl β-D galactopyranoside (X-gal). X-gal is a substrate for the enzyme β-D-galactosidase. Hydrolysis of the chromogen, Mag-caprylate, by lactose negative Salmonella species results in magenta colonies. The medium contains bile salts to inhibit the growth of Gram-positive organisms and the addition of the selective supplement solution increases the selectivity of the medium. Novobiocin inhibits Proteus growth and cefsulodin inhibits growth of pseudomonads.
Salt Meat Broth
Salmonella Rapid Test Elective Medium Composition per liter: Tryptone ............................................................10.0g Na2HPO4 .............................................................9.0g Sodium chloride..................................................5.0g Casein..................................................................5.0g KH2PO4 ...............................................................1.5g Malachite Green............................................0.0025g pH 6.5 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the Oxoid Salmonella Rapid Test which is for the presumptive detection of motile Salmonella.
Salmonella Rapid Test Elective Medium, 2X Composition per liter: Tryptone ............................................................20.0g Na2HPO4 ...........................................................18.0g Sodium chloride................................................10.0g Casein................................................................10.0g KH2PO4 ...............................................................3.0g Malachite Green..............................................0.005g pH 6.5 ± 0.2 at 25°C
383
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Do not autoclave. Cool to 45°–50°C. Pour into sterile Petri dishes in 20.0mL volumes. Allow the surface of the plates to dry before inoculation.
Use: For the selective isolation and differentiation of pathogenic enteric bacilli, especially those belonging to the genus Salmonella. This medium is not recommended for the primary isolation of Shigella species. Lactose-fermenting bacteria such as Escherichia coli or Klebsiella pneumoniae appear as small pink or red colonies. Lactose-nonfermenting bacteria—such as Salmonella species, Proteus species, and Shigella species—appear as colorless colonies. Production of H2S by Salmonella species turns the center of the colonies black.
Salmonella Shigella Agar, Modified (SS Agar, Modified) Composition per liter:
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C.
Agar ..................................................................12.0g Lactose..............................................................10.0g Sodium citrate...................................................10.0g Na2S2O3 ..............................................................8.5g Bile salts..............................................................5.5g Beef extract.........................................................5.0g Peptone ...............................................................5.0g Ferric citrate........................................................1.0g Neutral Red.....................................................0.025g Brilliant Green ...............................................0.33mg pH 7.3 ± 0.2 at 25°C
Use: For the presumptive detection of motile Salmo-
Source: This medium is available as a premixed
nella.
powder from Oxoid Unipath.
Preparation of Medium: Add components to
Salmonella Shigella Agar (SS Agar) Composition per liter: Agar ..................................................................13.5g Lactose ..............................................................10.0g Bile salts..............................................................8.5g Na2S2O3 ..............................................................8.5g Sodium citrate .....................................................8.5g Beef extract .........................................................5.0g Pancreatic digest of casein..................................2.5g Peptic digest of animal tissue..............................2.5g Ferric citrate........................................................1.0g Neutral Red .....................................................0.025g Brilliant Green ...............................................0.33mg pH 7.0 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems and Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Do not autoclave. Cool to 45°–50°C. Pour into sterile Petri dishes in 20.0mL volumes. Allow the surface of the plates to dry before inoculation.
Use: For the selective isolation and differentiation of pathogenic enteric bacilli, especially those belonging to the genus Salmonella. This medium provides better growth of Shigella species. Lactose-fermenting bacteria such as Escherichia coli or Klebsiella pneumoniae appear as small pink or red colonies. Lactosenonfermenting bacteria—such as Salmonella species, Proteus species, and Shigella species—appear as colorless colonies. Production of H2S by Salmonella species turns the center of the colonies black.
Salt Meat Broth Composition per liter: NaCl................................................................100.0g
384
Salt Tolerance Medium
Neutral ox-heart tissue ......................................30.0g Beef extract .......................................................10.0g Peptone..............................................................10.0g pH 7.6 ± 0.2 at 25°C
Source: This medium is available as tablets from Oxoid Unipath.
Use: For the cultivation and differentiation of Aeromonas and Plesiomonas species based on salt tolerance.
Salt Tolerance Medium Composition per liter:
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Beef heart, solids from infusion......................500.0g NaCl..................................................................65.0g Tryptose ............................................................10.0g pH 7.4 ± 0.2 at 25°C
Use: For the isolation and cultivation of staphylo-
Preparation of Medium: Add components to
Preparation of Medium: Add components to
cocci from specimens with a mixed flora such as fecal specimens, especially during the investigation of staphylococcal food poisoning.
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For testing the salt tolerance of a variety of mi-
Salt Tolerance Medium Composition per liter: Beef heart, infusion from ................................500.0g NaCl ..................................................................65.0g Tryptose ............................................................10.0g Glucose ...............................................................1.0g Indicator solution ............................................ 1.0mL pH 7.4 ± 0.2 at 25°C
Indicator Solution: Composition per 100.0mL:
croorganisms.
Salt Tolerance Medium, Gilardi Composition per liter: NaCl..................................................................65.0g Pancreatic digest of casein................................15.0g Agar ..................................................................15.0g Papaic digest of soybean meal............................5.0g pH 7.3 ± 0.2 at 25°C
Preparation of Medium: Add components to
cresol Purple to ethanol. Mix thoroughly.
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Do not overheat. Pour into sterile Petri dishes or leave in tubes.
Preparation of Medium: Add components to
Use: For the cultivation and maintenance of salt-tol-
Bromcresol Purple ..............................................1.6g Ethanol (95% solution) ............................... 100.0mL
Preparation of Indicator Solution: Add Brom-
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
erant, nonfermenting Gram-negative bacteria. For the differentiation of nonfermenting Gram-negative bacteria based on salt tolerance.
Use: For the cultivation of salt-tolerant Streptococcus species and other salt-tolerant Gram-positive cocci. For the differentiation of Gram-positive cocci based on salt tolerance.
Salt Tolerance Medium Composition per liter: NaCl ..................................................................60.0g Peptone................................................................5.0g Yeast extract........................................................2.0g Beef extract .........................................................1.0g pH 7.4 ± 0.2 at 25°C
Salt Tolerance Medium, Tatum Composition per liter: NaCl..................................................................65.0g Peptone ...............................................................5.0g Yeast extract........................................................2.0g Beef extract.........................................................1.0g pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Preparation of Medium: Add components to
Use: For the cultivation of salt-tolerant, nonferment-
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
ing Gram-negative bacteria. For the differentiation of nonfermenting Gram-negative bacteria based on salt tolerance.
Schaedler Agar
Sauton’s Medium
385
Source: This medium is available as a premixed
Composition per liter:
powder from BD Diagnostic Systems.
L-Asparagine .......................................................4.0g
Preparation of Medium: Add components to
Citric acid............................................................2.0g K2HPO4 ...............................................................0.5g MgSO4 ................................................................0.5g Triton WR 1339 ................................................0.25g Ferric ammonium citrate...................................0.05g Glycerol ........................................................ 40.0mL
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of Mycobacterium tuberculosis Bacille Calmette-Guèrin (BCG) for vaccine production.
SBG Enrichment Broth (Selenite Brilliant Green Enrichment Broth) Composition per liter: D-Mannitol
..........................................................5.0g Peptone................................................................5.0g Yeast extract........................................................5.0g Na2SeO3·5H2O....................................................4.0g K2HPO4 .............................................................2.65g KH2PO4 .............................................................1.02g Sodium taurocholate ...........................................1.0g Brilliant Green .................................................5.0mg pH 7.2 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Continue boiling for 5–10 min. Do not autoclave. Distribute into sterile tubes or flasks.
Use: For the selective isolation of Salmonella species.
SBG Sulfa Enrichment Composition per liter: D-Mannitol
..........................................................5.0g Peptone................................................................5.0g Yeast extract........................................................5.0g Na2SeO3·5H2O....................................................4.0g K2HPO4 .............................................................2.65g KH2PO4 .............................................................1.02g Sodium taurocholate ...........................................1.0g Sodium sulfapyridine..........................................0.5g Brilliant Green .................................................5.0mg pH 7.2 ± 0.2 at 25°C
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Continue boiling for 5–10 min. Do not autoclave. Distribute into sterile tubes or flasks.
Use: For the selective isolation of Salmonella species.
SCGYEM Medium Composition per liter: Casein, isoelectric .............................................10.0g Yeast extract....................................................... 5.0g Glucose ...............................................................2.5g Na2HPO4 .........................................................1.325g KH2PO4...............................................................0.8g Calf serum, heat inactivated ....................... 100.0mL
Preparation of Medium: Add components, except calf serum, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Autoclave for 30 min at 15 psi pressure–121°C. Cool to 25°C. Aseptically add 100.0mL of sterile, heat-inactivated calf serum. Mix thoroughly. Aseptically distribute into sterile, screw-capped tubes or flasks.
Use: For the cultivation of Naegleria australiensis and Naegleria fowleri.
Schaedler Agar (Schaedler Anaerobic Agar) Composition per liter: Agar ..................................................................13.5g Glucose .............................................................5.83g Pancreatic digest of casein..................................5.7g Proteose peptone no. 3........................................5.0g Yeast extract........................................................5.0g Tris(hydroxymethyl)aminomethane buffer.........3.0g NaCl..................................................................1.65g Papaic digest of soybean meal............................1.0g K2HPO4.............................................................0.83g L-Cystine .............................................................0.4g Hemin ...............................................................0.01g pH 7.6 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems and Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
386
Schaedler Agar
Use: For the isolation, cultivation, and enumeration of anaerobic and aerobic microorganisms.
Schaedler Agar Composition per liter: Agar ..................................................................13.5g Pancreatic digest of casein..................................8.2g Glucose ...............................................................5.8g Yeast extract........................................................5.0g Tris(hydroxymethyl)aminomethane buffer.........3.0g Peptic digest of animal tissue..............................2.5g NaCl ....................................................................1.7g Papaic digest of soybean meal ............................1.0g K2HPO4 ...............................................................0.8g L-Cystine .............................................................0.4g Hemin................................................................0.01g pH 7.6 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the isolation, cultivation, and enumeration of anaerobic and aerobic microorganisms.
Schaedler Agar with Vitamin K1 and Sheep Blood Composition per liter: Agar ..................................................................13.5g Pancreatic digest of casein..................................8.2g Glucose ...............................................................5.8g Yeast extract........................................................5.0g Tris(hydroxymethyl)aminomethane buffer.........3.0g Peptic digest of animal tissue..............................2.5g Papaic digest of soybean meal ............................1.0g NaCl ....................................................................1.7g K2HPO4 ...............................................................0.8g L-Cystine .............................................................0.4g Hemin................................................................0.01g Sheep blood, defibrinated ............................. 50.0mL Vitamin K1 solution ........................................ 1.0mL pH 7.6 ± 0.2 at 25°C
Vitamin K1 Solution: Composition per 10.0mL: Vitamin K1 ..........................................................5.0g Ethanol, absolute........................................... 10.0mL
Preparation of Vitamin K1 Solution: Add vitamin K1 to ethanol. Mix thoroughly.
Preparation of Medium: Add components, except sheep blood, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile sheep blood. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the recovery of fastidious anaerobic bacteria such as Bacteroides species.
Schaedler Broth (Schaedler Anaerobic Broth) Composition per liter: Pancreatic digest of casein..................................8.2g Glucose ...............................................................5.8g Yeast extract........................................................5.0g Tris(hydroxymethyl)aminomethane buffer.........3.0g Peptic digest of animal tissue .............................2.5g NaCl....................................................................1.7g Papaic digest of soybean meal............................1.0g K2HPO4...............................................................0.8g L-Cystine .............................................................0.4g Hemin ...............................................................0.01g pH 7.6 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems and Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation and maintenance of Eubacterium combesii, Eubacterium contortum, and a variety of other anaerobic bacteria.
Schaedler CNA Agar with Vitamin K1 and Sheep Blood
Composition per liter:
Agar ..................................................................13.5g Pancreatic digest of casein..................................8.2g Glucose ...............................................................5.8g Yeast extract........................................................5.0g Tris(hydroxymethyl)aminomethane buffer.........3.0g Peptic digest of animal tissue .............................2.5g Papaic digest of soybean meal............................1.0g NaCl....................................................................1.7g K2HPO4...............................................................0.8g L-Cystine .............................................................0.4g Hemin ...............................................................0.01g Colistin..............................................................0.01g Nalidixic acid....................................................0.01g
Selenite Broth Sheep blood, defibrinated ............................. 50.0mL Vitamin K1 solution ........................................ 1.0mL pH 7.6 ± 0.2 at 25°C
Vitamin K1 Solution: Composition per 10.0mL: Vitamin K1 ..........................................................5.0g Ethanol, absolute........................................... 10.0mL
Preparation of Vitamin K1 Solution: Add vitamin K1 to ethanol. Mix thoroughly.
Preparation of Medium: Add components, except sheep blood, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile sheep blood. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the selective isolation of anaerobic, Grampositive cocci, especially Peptococcus species and Peptostreptococcus species.
Schaedler KV Agar with Vitamin K1 and Sheep Blood
Composition per liter:
Agar ..................................................................13.5g Pancreatic digest of casein..................................8.2g Glucose ...............................................................5.8g Yeast extract........................................................5.0g Tris(hydroxymethyl)aminomethane buffer.........3.0g Peptic digest of animal tissue..............................2.5g NaCl ....................................................................1.7g Papaic digest of soybean meal ............................1.0g K2HPO4 ...............................................................0.8g L-Cystine .............................................................0.4g Hemin................................................................0.01g Kanamycin ........................................................0.01g Vancomycin .....................................................7.5mg Sheep blood, defibrinated ............................ 50.0 mL Vitamin K1 solution ........................................ 1.0mL pH 7.6 ± 0.2 at 25°C
Vitamin K1 Solution: Composition per 10.0mL: Vitamin K1 ..........................................................5.0g Ethanol, absolute........................................... 10.0mL
Preparation of Vitamin K1 Solution: Add vitamin K1 to ethanol. Mix thoroughly.
Preparation of Medium: Add components, except sheep blood, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile sheep blood. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
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Use: For the selective isolation of Gram-negative anaerobic bacteria.
Schleifer-Krämer Agar (SK Agar) Composition per liter: Agar ..................................................................13.0g Glycerol ............................................................10.0g Sodium pyruvate...............................................10.0g Pancreatic digest of casein................................10.0g Beef extract.........................................................5.0g Yeast extract........................................................3.0g Potassium isothiocyanate..................................2.25g LiCl .....................................................................2.0g Na2HPO4·2H2O...................................................0.9g NaH2PO4·H2O.....................................................0.6g Glycine................................................................0.5g NaN3 solution ............................................... 10.0mL pH 7.2 ± 0.2 at 25°C
NaN3 Solution: Composition per 10.0mL: NaN3 ...............................................................0.045g
Preparation of NaN3 Solution: Add NaN3 to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except NaN3 solution, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Adjust pH to 7.2. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile NaN3 solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation and cultivation of Staphylococcus species.
Selenite Broth (Selenite Broth, Lactose) (Selenite F Enrichment Medium) (Sodium Biselenite Medium) (Sodium Hydrogen Selenite Medium) Composition per liter: Na2HPO4 ...........................................................10.0g Pancreatic digest of casein..................................5.0g Lactose................................................................4.0g NaHSeO3·5H2O ..................................................4.0g pH 7.0 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems and a prepared medium from Oxoid Unipath.
388
Selenite Broth Base, Mannitol
Caution: Sodium biselenite is toxic and a potential teratogen and care must be taken to avoid inhalation of the powdered dye, contact with the skin, or ingestion, especially in pregnant laboratory workers.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Do not autoclave. Distribute into sterile tubes in 10.0mL volumes.
Use: For the isolation and enrichment of Salmonella species from clinical specimens.
Selenite Broth Base, Mannitol Composition per liter: Na2HPO4 ...........................................................10.0g Peptone................................................................5.0g Mannitol..............................................................4.0g NaHSeO3·5H2O ..................................................4.0g pH 7.1 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath. Caution: Sodium selenite is toxic and a potential teratogen and care must be taken to avoid inhalation of the powdered dye, contact with the skin, or ingestion, especially in pregnant laboratory workers.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat. Do not autoclave. Distribute into sterile tubes in 10.0mL volumes. Sterilize for 10 min at 0 psi pressure–100°C.
Use: For the isolation and cultivation of Salmonella typhi and Salmonella paratyphi.
Selenite Cystine Broth Composition per liter: Na2HPO4 ...........................................................10.0g Pancreatic digest of casein..................................5.0g Lactose ................................................................4.0g Na2SeO3·5H2O....................................................4.0g L-Cystine ...........................................................0.02g pH 7.0 ± 0.2 at 25°C
tribute into sterile tubes in 10.0mL volumes. Sterilize for 15 min at 0 psi pressure–100°C.
Use: For the isolation and cultivation of Salmonella species from feces and other specimens.
Selenite F Broth Composition per liter: KH2PO4...............................................................7.0g Pancreatic digest of casein..................................5.0g Lactose................................................................4.0g Na2SeO3·5H2O....................................................4.0g Na2HPO4 .............................................................3.0g pH 7.0 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Caution: Sodium selenite is toxic and a potential teratogen and care must be taken to avoid inhalation of the powdered dye, contact with the skin, or ingestion, especially in pregnant laboratory workers.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat. Do not autoclave. Distribute into sterile tubes in 10.0mL volumes. Sterilize for 30 min at 0 psi pressure–100°C.
Use: For the isolation and cultivation of Salmonella species from feces and other specimens.
Semisolid Brucella Broth Composition per liter: Peptone .............................................................10.0g Pancreatic digest of casein................................10.0g NaCl....................................................................5.0g Yeast extract........................................................2.0g Agar ....................................................................1.6g D-Glucose............................................................1.0g
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of Campylobacter species.
Source: This medium is available as a premixed powder from BD Diagnostic Systems and Oxoid Unipath.
Caution: Sodium selenite is toxic and a potential teratogen and care must be taken to avoid inhalation of the powdered dye, contact with the skin, or ingestion, especially in pregnant laboratory workers.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat. Do not autoclave. Dis-
Semisolid Medium for Motility Composition per liter: Biosate ................................................................5.0g Polypeptone ........................................................5.0g NaCl....................................................................5.0g Agar ....................................................................4.0g Myosate...............................................................1.5g Triphenyltetrazolium chloride solution .......... 2.5mL pH 6.9–7.1at 25°C
Serratia Hd-MHr Triphenyltetrazolium Chloride Solution: Composition per 10.0mL: Triphenyltetrazolium chloride ............................0.1g Ethanol (95% solution) ................................. 10.0mL
Preparation of Triphenyltetrazolium Chloride Solution: Add triphenyltetrazolium chloride to 10.0mL of ethanol. Mix thoroughly.
Preparation of Medium: Add components, except triphenyltetrazolium chloride solution, to distilled/deionized water and bring volume to 997.5mL. Mix thoroughly. Gently heat and bring to boiling. Add 2.5mL of triphenyltetrazolium chloride solution. Mix thoroughly. Distribute into tubes in 10.0mL volumes. Autoclave for 15 min at 15 psi pressure– 121°C.
Use: For the differentiation of bacteria based on motility.
Sensitest Agar Composition per liter: Pancreatic digest of casein................................11.0g Agar ....................................................................8.0g Buffer salts ..........................................................3.3g Peptone................................................................3.0g NaCl ....................................................................3.0g Glucose ...............................................................2.0g Starch ..................................................................1.0g Nucleoside bases...............................................0.02g Thiamine ........................................................0.02mg pH 7.4 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes.
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Agar ....................................................................0.4g Irgasan inhibitor.............................................. 1.0mL Indicator solution ............................................ 1.0mL
Preparation of Solution A: Add components to distilled/deionized water and bring volume to 92.0mL. Mix thoroughly. Adjust pH to 6.7 with 1N NaOH. Irgasan Inhibitor: Composition per 100.0mL: Irgasan-DP-300 (4,2´, 4´-trichloro2-hydroxydiphenylether) ..............................0.1g NaOH (1N solution)...................................... 10.0mL
Preparation of Irgasan Inhibitor: Add irgasan to 10.0mL of NaOH solution. Mix thoroughly. Gently heat to dissolve. Bring volume to 100.0mL with distilled/deionized water.
Indicator Solution: Composition per 100.0mL: Bromthymol Blue ...............................................0.2g Phenol Red..........................................................0.1g
Preparation of Indicator Solution: Add components to 50.0mL of distilled/deionized water. Mix thoroughly for 1h. Bring volume to 100.0mL with distilled/deionized water.
Solution B: Composition per 10.0mL: L-Arabinose .........................................................1.0g
Preparation of Solution B: Add L-arabinose to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Preparation of Medium: Combine 92.0mL of solution A with 10.0mL of solution B. Mix thoroughly. Distribute into tubes. Autoclave for 15 min at 15 psi pressure–121°C. Allow tubes to cool in an upright position.
Use: For the cultivation and differentiation of Serratia
Composition per 102.0mL:
species based on the fermentation of arabinose and production of ornithine decarboxylase. Serratia marcescens changes the medium to purple throughout the tube. Serratia liquefaciens changes the medium to a band of purple at the top of the tube with a green/yellow butt. Serratia rubidaea changes the medium to yellow throughout the tube.
Solution A ..................................................... 92.0mL Solution B ..................................................... 10.0mL pH 6.7 ± 0.2 at 25°C
Composition per liter:
Use: For the performance of antibiotic sensitivity assays.
Serratia Differential Medium (SD Medium)
Solution A: Composition per 92.0mL: Yeast extract........................................................1.0g L-Ornithine ..........................................................1.0g NaCl ....................................................................0.5g
Serratia Hd-MHr Agar ..................................................................15.0g K2HPO4...............................................................7.0g Glucose ...............................................................5.0g KH2PO4...............................................................3.0g 2-Methyl-DL-histidine·2HCl ...............................1.0g
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Serratia Medium
Serum Glucose Agar (Serum Dextrose Agar) (ATCC Medium 287)
(NH4)2SO4...........................................................1.0g MgSO4·7H2O ......................................................0.5g
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of Serratia marcescens.
Serratia Medium (ATCC Medium 181) Composition per liter: Agar ..................................................................20.0g Pancreatic digest of casein..................................5.0g Yeast extract........................................................5.0g Glucose ...............................................................1.0g K2HPO4 ...............................................................1.0g pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of Serratia marcescens.
Serratia Medium (ATCC Medium 1399) Composition per liter: Agar ..................................................................15.0g K2HPO4 ...............................................................7.0g Glucose ...............................................................5.0g KH2PO4 ...............................................................3.0g Casein hydrolysate..............................................1.0g (NH4)2SO4...........................................................1.0g Yeast extract........................................................1.0g MgSO4·7H2O ......................................................0.1g pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of Serratia marcescens.
Composition per 1060.0mL: Agar ..................................................................15.0g Peptone .............................................................10.0g Beef extract.........................................................5.0g NaCl....................................................................5.0g Serum-glucose solution ................................ 60.0mL pH 7.3 ± 0.2 at 25°C
Serum-Glucose Solution: Composition per 60.0mL: D-Glucose ..........................................................10.0g
Serum (inactivated at 56°C, 30 min) ............ 50.0mL
Preparation of Serum-Glucose Solution: Add glucose to 50.0mL of heat-inactivated serum. Horse serum or ox serum may be used. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except serum-glucose solution, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 10 psi pressure–115°C. Cool to 50°C. Aseptically add 60.0mL of sterile serum-glucose solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes. Allow tubes to cool in a slanted position.
Use: For the cultivation and maintenance of Brucella species.
Serum Glucose Agar, Farrell Modified Composition per 1086.9mL: Agar ..................................................................15.0g Peptone .............................................................10.0g Beef extract.........................................................5.0g NaCl....................................................................5.0g Serum-glucose solution ................................ 60.0mL Bacitracin solution ........................................ 12.5mL Cycloheximide solution ................................ 10.0mL Nystatin solution............................................. 2.0mL Polymyxin B solution ..................................... 1.0mL Nalidixic acid solution.................................... 1.0mL Vancomycin solution ...................................... 0.4mL pH 7.3 ± 0.2 at 25°C
Serum-Glucose Solution: Composition per 60.0mL: D-Glucose ..........................................................10.0g
Serum (inactivated at 56°C, 30 min) ............ 50.0mL
Preparation of Serum-Glucose Solution: Add glucose to 50.0mL of heat-inactivated serum. Horse serum or ox serum may be used. Mix thoroughly. Filter sterilize.
Serum Tellurite Agar Bacitracin Solution: Composition per 12.5mL: Bacitracin .....................................................25,000U
Preparation of Bacitracin Solution: Add bacitracin to distilled/deionized water and bring volume to 12.5mL. Mix thoroughly. Filter sterilize.
Cycloheximide Solution: Composition per 100.0mL: Cycloheximide ....................................................1.0g Acetone ........................................................... 5.0mL
Preparation of Cycloheximide Solution: Add cycloheximide to 5.0mL of acetone. Mix thoroughly. Bring volume to 100.0mL with distilled/deionized water. Mix thoroughly. Filter sterilize.
Nystatin Solution: Composition per 5.0mL: Nystatin......................................................250,000U
Preparation of Nystatin Solution: Add nystatin to distilled/deionized water and bring volume to 5.0mL. Mix thoroughly. Filter sterilize. Polymyxin B Solution: Composition per 2.0mL: Polymyxin B ................................................10,000U
Preparation of Polymyxin B Solution: Add polymyxin B to distilled/deionized water and bring volume to 2.0mL. Mix thoroughly. Filter sterilize.
Nalidixic Acid Solution: Composition per 2.0mL: Nalidixic acid ......................................................0.1g NaOH (0.5N solution)..................................... 2.0mL
Preparation of Nalidixic Acid Solution: Add nalidixic acid to 2.0mL of NaOH solution. Mix thoroughly. Immediately before use, add 1.0mL of this stock solution to 9.0mL of distilled/deionized water. Mix thoroughly. Filter sterilize.
Vancomycin Solution: Composition per 1.0mL: Vancomycin ......................................................0.05g
Preparation of Vancomycin Solution: Add vancomycin to distilled/deionized water and bring volume to 1.0mL. Mix thoroughly. Filter sterilize. Preparation of Medium: Add components—except serum-glucose solution, bacitracin solution, cycloheximide solution, nystatin solution, polymyxin B solution, nalidixic acid solution, and vancomycin solution—to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 10 psi pressure– 115°C. Cool to 50°C. Aseptically add 60.0mL of sterile serum-glucose solution, 12.5mL of sterile ba-
391
citracin solution, 10.0mL of sterile cycloheximide solution, 2.0mL of sterile nystatin solution, 1.0mL of sterile polymyxin B solution, 1.0mL of sterile nalidixic acid solution, and 0.4mL of sterile vancomycin solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes. Allow tubes to cool in a slanted position.
Use: For the selective isolation and cultivation of Brucella species.
Serum Potato Infusion Agar Composition per 1120.0mL: Agar ..................................................................15.0g Peptone .............................................................10.0g Meat extract ........................................................5.0g NaCl....................................................................5.0g Potato infusion ................................................... 1.0L Horse serum, heat inactivated..................... 100.0mL Glycerol ........................................................ 20.0mL pH 6.8 ± 0.2 at 25°C
Potato Infusion: Composition per 10.0mL: Potatoes...........................................................250.0g
Preparation of Potato Infusion: Add peeled, thinly sliced potatoes to 1.0L of distilled/deionized water. Infuse overnight at 60°C. Filter through Whatman no. 1 filter paper. Bring volume to 1.0L with distilled/deionized water.
Preparation of Medium: Combine components, except horse serum. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 100.0mL of sterile horse serum. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation of Brucella species.
Serum Tellurite Agar Composition per liter: Agar ..................................................................20.0g Pancreatic digest of casein................................10.0g Peptic digest of animal tissue ...........................10.0g NaCl....................................................................5.0g Glucose ...............................................................2.0g Lamb serum .................................................. 50.0mL Chapman tellurite solution............................ 10.0mL pH 7.5 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Chapman Tellurite Solution: Composition per 100.0mL: K2TeO3 ................................................................1.0g
392
Seven H11 Agar
Preparation of Chapman Tellurite Solution: Add K2TeO3 to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except lamb serum and Chapman tellurite solution, to distilled/deionized water and bring volume to 940.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C. Aseptically add sterile lamb serum and 10.0mL of sterile Chapman tellurite solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation and cultivation of Corynebacterium species, especially in the laboratory diagnosis of diphtheria.
Seven H11 Agar (Selective 7H11 Agar) Composition per 1010.0mL: Agar ..................................................................13.5g KH2PO4 ...............................................................1.5g Na2HPO4 .............................................................1.5g Pancreatic digest of casein..................................1.0g NaCl ..................................................................0.85g Monosodium glutamate ......................................0.5g (NH4)2SO4...........................................................0.5g Sodium citrate .....................................................0.4g MgSO4·7H2O ....................................................0.05g Ferric ammonium citrate...................................0.04g CuSO4·5H2O ....................................................1.0mg Pyridoxine........................................................1.0mg ZnSO4·7H2O ....................................................1.0mg Biotin ...............................................................0.5mg CaCl2·2H2O......................................................0.5mg Malachite Green.............................................0.25mg Middlebrook OADC enrichment ................ 100.0mL Antibiotic inhibitor ....................................... 10.0mL Glycerol .......................................................... 5.0mL pH 6.6 ± 0.2 at 25°C
Source: This medium is available as a prepared medium from BD Diagnostic Systems.
Middlebrook OADC Enrichment: Bovine albumin fraction V .................................5.0g Glucose ...............................................................2.0g NaCl ..................................................................0.85g Catalase............................................................3.0mg Oleic acid ...................................................... 0.06mL
Preparation of Middlebrook OADC Enrichment: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Antibiotic Inhibitor: Composition per 10.0mL: Carbenicillin .....................................................0.05g Trimethoprim lactate.........................................0.02g Amphotericin B ................................................0.01g Polymyxin B .............................................. 200,000U
Preparation of Antibiotic Inhibitor: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add glycerol to 900.0mL of distilled/deionized water. Mix thoroughly. Add remaining components, except Middlebrook OADC enrichment and antibiotic inhibitor. Mix thoroughly. Gently heat. Do not boil. Autoclave for 10 min at 15 psi pressure–121°C. Cool to 50°–55°C. Aseptically add 100.0mL of sterile Middlebrook OADC enrichment and 10.0mL of sterile antibiotic solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation and cultivation of Mycobacterium species from specimens with a mixed flora.
SF Broth (Streptococcus faecalis Broth) Composition per liter: Pancreatic digest of casein................................20.0g Glucose ...............................................................5.0g NaCl....................................................................5.0g K2HPO4...............................................................4.0g KH2PO4...............................................................1.5g NaN3 ...................................................................0.5g Bromcresol Purple ..........................................0.032g pH 6.9 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation and differentiation of group D enterococci (Streptococcus faecalis and Streptococcus faecium) from group D nonenterococci and from other Streptococcus species. Group D enterococci turn the medium turbid and yellow-brown.
Shigella Broth Composition per liter: Pancreatic digest of casein................................20.0g NaCl....................................................................5.0g K2HPO4...............................................................2.0g KH2PO4...............................................................2.0g Glucose ...............................................................1.0g
Simmons’ Citrate Agar Novobiocin solution...................................... 11.1mL Tween 80......................................................... 1.5mL pH 7.0 ± 0.2 at 25°C
Novobiocin Solution: Composition per liter: Novobiocin........................................................0.05g
Preparation of Novobiocin Solution: Add novobiocin to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, ex-
393
Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes in 15.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C. Allow tubes to cool in an upright position.
Use: For the differentiation of members of the Enterobacteriaceae based on H2S production, indole production, and motility.
SIM Medium Composition per liter:
cept novobiocin solution, to distilled/deionized water and bring volume to 988.9mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile novobiocin solution. Mix thoroughly. Aseptically distribute into sterile tubes.
Pancreatic digest of casein................................20.0g Peptic digest of animal tissue .............................6.1g Agar ....................................................................3.5g Fe(NH4)2(SO4)2·6H2O ........................................0.2g Na2S2O3·5H2O ....................................................0.2g pH 7.3 ± 0.2 at 25°C
Use: For the isolation and cultivation of Shigella species.
Source: This medium is available as a premixed
Sierra Medium
Preparation of Medium: Add components to
Composition per liter: Agar ..................................................................15.0g Peptone..............................................................10.0g NaCl ....................................................................5.0g CaCl2·H2O...........................................................0.1g Tween 80....................................................... 10.0mL pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components, except Tween 80, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Separately autoclave Tween 80 for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 10.0mL of sterile Tween 80. Mix thoroughly. Pour into sterile Petri dishes.
Use: For the differentiation of bacteria based on lipase activity. Bacteria with lipase activity form colonies surrounded by a white precipitate.
SIM Medium Composition per liter: Peptone..............................................................30.0g Agar ....................................................................3.0g Beef extract .........................................................3.0g Peptonized iron ...................................................0.2g Na2S2O3·5H2O ................................................0.025g pH 7.3 ± 0.2 at 25°C
powder from BD Diagnostic Systems and Oxoid Unipath. distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes in 15.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C. Allow tubes to cool in an upright position.
Use: For the differentiation of members of the Enterobacteriaceae based on H2S production, indole production, and motility.
Simmons’ Citrate Agar (Citrate Agar) Composition per liter: Agar ..................................................................15.0g NaCl....................................................................5.0g Sodium citrate.....................................................2.0g K2HPO4...............................................................1.0g (NH4)H2PO4........................................................1.0g MgSO4·7H2O ......................................................0.2g Bromthymol Blue .............................................0.08g pH 6.9 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems and Oxoid Unipath.
Preparation of Medium: Add components to
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Preparation of Medium: Add components to
Use: For the differentiation of Gram-negative bacte-
distilled/deionized water and bring volume to 1.0L.
ria on the basis of citrate utilization. Bacteria that can
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Skim Milk Agar
utilize citrate as sole carbon source turn the medium blue.
Preparation of Antibiotic Solution: Add com-
Skim Milk Agar
Preparation of Medium: To 940.0mL of sterile cooled blood agar base no. 2, aseptically add 50.0mL of sterile, lysed defibrinated horse blood and 10.0mL of sterile antibiotic solution. Pour into sterile Petri dishes or distribute into sterile tubes.
Composition per 1100.0mL: Agar ..................................................................15.0g Pancretic digest of casein....................................5.0g Yeast extract........................................................2.5g Glucose ...............................................................1.0g Skim milk solution...................................... 100.0mL pH 7.0 ± 0.1 at 25°C
Preparation of Skim Milk Solution: Add skim
ponents to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Use: For the selective isolation and cultivation of Campylobacter species.
SM ID2 Agar
milk solids to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Composition per liter:
Preparation of Medium: Add components, ex-
Use: A new chromogenic medium for the selective
Proprietary
Source: This medium is available from bioMérieux.
cept skim milk solution, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C. Aseptically add 100.0mL of cooled, sterile skim milk solution. Mix thoroughly. Pour into sterile Petri dishes or aseptically distribute into sterile tubes.
isolation and detection of Salmonella, S. typhi, and S. paratyphi and most Lactose(+) Salmonella present pale pink to mauve colonies. Other organisms are either inhibited, colorless, or pale blue in appearance.
Use: For the cultivation and differentiation of bacte-
Glucose .............................................................20.0g Agar ..................................................................16.0g Pancreatic digest of casein................................13.5g Yeast extract........................................................6.5g NaCl....................................................................5.0g Bromcresol Green.............................................0.02g pH 4.8 ± 0.2 at 25°C
ria based on proteolytic activity.
Skirrow Brucella Medium Composition per liter: Blood agar base no. 2.................................. 940.0mL Horse blood, lysed defibrinated .................... 50.0mL Antibiotic solution ........................................ 10.0mL pH 7.4 ± 0.2 at 25°C
Blood Agar Base No. 2 Composition per 940.0mL: Proteose peptone ...............................................15.0g Agar ..................................................................12.0g NaCl ....................................................................5.0g Yeast extract........................................................5.0g Liver digest .........................................................2.5g pH 7.4 ± 0.2 at 25°C
Preparation of Blood Agar Base No. 2: Add components to distilled/deionized water and bring volume to 940.0mL. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Antibiotic Solution: Composition per 10.0mL: Vancomycin ......................................................0.01g Trimethoprim ...................................................5.0mg Polymyxin B ...................................................2500U
Snyder Agar Composition per liter:
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes in 10.0mL volumes. Autoclave for 15 min at 13 psi pressure–118°C. Do not overheat. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and enumeration of lactobacilli in saliva and indication of dental caries activity.
Snyder Test Agar Composition per liter: Agar ..................................................................20.0g Glucose .............................................................20.0g Tryptose ............................................................20.0g NaCl....................................................................5.0g Bromcresol Green.............................................0.02g pH 4.8 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Sodium Hippurate Broth Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes in 10.0mL volumes. Autoclave for 15 min at 13 psi pressure–118°C. Do not overheat. Pour into sterile Petri dishes or leave in tubes.
and horse serum. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation of Pseudomonas aeruginosa.
Sodium Chloride Sucrose Medium 900 with Penicillin G
Use: For the cultivation and enumeration of lactobacilli in saliva and indication of dental caries activity.
Sodium Chloride Broth, 6.5 Composition per liter: Beef heart, solids from infusion......................500.0g NaCl ..................................................................65.0g Tryptose ............................................................10.0g pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of enterococci and other salt-tolerant organisms. For the differentiation of microorganisms based on salt tolerance.
Sodium Chloride Sucrose Medium 900 (Sodium Chloride SUC Medium 900)
395
Composition per liter: Sucrose..............................................................97.3g Pancreatic digest of gelatin...............................14.5g NaCl..................................................................14.3g Agar ..................................................................13.3g Brain heart, solids from infusion ........................6.0g Peptic digest of animal tissue .............................6.0g Yeast extract........................................................5.0g Glucose ...............................................................3.0g Na2HPO4 .............................................................2.5g MgSO4 ..............................................................0.25g Horse serum (γ-globulin free, inactivated 30 min at 56°C).............. 100.0mL Penicillin solution ......................................... 10.0mL pH 7.4 ± 0.2 at 25°C
Penicillin Solution: Composition per 10.0mL: Penicillin G ................................................ 500,000U
Composition per liter:
Preparation of Penicillin Solution: Add peni-
Sucrose..............................................................97.3g Pancreatic digest of gelatin ...............................14.5g NaCl ..................................................................14.3g Agar ..................................................................13.3g Brain heart, solids from infusion ........................6.0g Peptic digest of animal tissue..............................6.0g Yeast extract........................................................5.0g Glucose ...............................................................3.0g Na2HPO4 .............................................................2.5g MgSO4 ..............................................................0.25g Horse serum (γ-globulin free, inactivated 30 min at 56°C).............. 100.0mL Carbenicillin solution.................................... 10.0mL pH 7.4 ± 0.2 at 25°C
cillin G to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Carbenicillin Solution: Composition per 10.0mL: Carbenicillin........................................................5.0g
Preparation of Carbenicillin Solution: Add carbenicillin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except carbenicillin solution and horse serum, to distilled/deionized water and bring volume to 890.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add carbenicillin solution
Preparation of Medium: Add components, except penicillin solution and horse serum, to distilled/ deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add penicillin solution and horse serum. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation of Pseudomonas aeruginosa.
Sodium Hippurate Broth (Hippurate Broth) Composition per liter: Beef heart, solids from infusion......................500.0g Tryptose ............................................................10.0g Sodium hippurate..............................................10.0g NaCl....................................................................5.0g pH 7.4 ± 0.2 at 25°C
Source: Heart infusion broth is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L.
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Soft Agar Gelatin Overlay
Mix thoroughly. Gently heat and bring to boiling. Distribute into screw-capped tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Tighten caps to prevent drying.
Use: For the identification and differentiation of βhemolytic streptococci based on hippurate hydrolysis. After inoculation and incubation, tubes are treated with FeCl3 reagent. A heavy precipitate remaining after 10–15 min indicates that hippurate has been hydrolyzed.
Soft Agar Gelatin Overlay Composition per plate: Base agar....................................................... 15.0mL Soft agar gelatin overlay ................................. 2.5mL pH 7.0 ± 0.2 at 25°C
Base Agar: Composition per liter: Agar ..................................................................15.0g Peptone................................................................5.0g NaCl ....................................................................5.0g Beef extract .........................................................3.0g MnSO4·H2O ......................................................0.05g
Preparation of Base Agar: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Soft Agar Gelatin Overlay: Composition per liter: Gelatin...............................................................15.0g Agar ....................................................................8.0g Peptone................................................................5.0g NaCl ....................................................................5.0g Beef extract .........................................................3.0g MnSO4·H2O ......................................................0.05g
Preparation of Soft Agar Gelatin Overlay: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Preparation of Medium: Aseptically pour cooled, sterile base agar into sterile Petri dishes in 15.0mL volumes. Allow agar to solidify. Inoculate plates with samples. Overlay each plate with 2.5mL of soft agar gelatin overlay.
Use: For the cultivation and differentiation of microorganisms based on proteolytic activity.
Sorbitol MacConkey Agar (MacConkey Agar with Sorbitol) Composition per liter: Peptone..............................................................20.0g
Agar ..................................................................15.0g Sorbitol .............................................................10.0g NaCl....................................................................5.0g Bile salts no. 3.....................................................1.5g Neutral Red.......................................................0.03g Crystal Violet ...................................................1.0mg pH 7.1 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems and Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the isolation and cultivation of pathogenic Escherichia coli.
Sorbitol MacConkey Agar with BCIG (SMAC with BCIG) Composition per liter: Peptone .............................................................20.0g Agar ..................................................................15.0g Sorbitol .............................................................10.0g NaCl....................................................................5.0g Proteose peptone.................................................3.0g Bile salts mixture ................................................1.5g 5-Bromo-4-chloro-3-indolyl-β-D-glucuronide sodium salt....................................................0.1g Neutral Red.......................................................0.03g pH 7.1 ± 0.2 at 25°C
Source: This medium is available from Oxoid. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Pour into sterile Petri dishes.
Use: A selective and differential medium for the detection of Escherichia coli O157 incorporating the chromogen 5-bromo-4-chloro-3-indolyl-β-D-glucuronide (BCIG). The medium combines two different screening mechanisms for the detection of E. coli O157, the failure to ferment sorbitol and the absence of β-glucuronidase activity. The nonsorbitol-fermenting and β-glucuronidase-negative E. coli O157 will appear as straw colored colonies. Organisms with β-glucuronidase activity will cleave the substrate, leading to a distinct blue-green coloration of the colonies.
SS Deoxycholate Agar
Soy Peptone Broth Composition per liter: Papaic digest of soybean meal ..........................20.0g NaCl ....................................................................5.0g Phenol Red (2% solution) ............................... 1.0mL pH 7.3 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.3. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the isolation and cultivation of Mycoplasma species and Ureaplasma species.
Specimen Preservative Medium Composition per liter: NaCl ....................................................................5.0g Sodium citrate·2H2O...........................................5.0g (NH4)2HPO4 ........................................................4.0g KH2PO4 ...............................................................2.0g Yeast extract........................................................1.0g Sodium deoxycholate..........................................0.5g MgSO4·7H2O ......................................................0.4g Glycerol ...................................................... 300.0mL pH 7.0 ± 0.2 at 25°C
397
deionized water and bring volume to 990.0mL. Mix thoroughly. Adjust pH to 7.4. Add agar. Gently heat and bring to boiling. Distribute into tubes in 9.0mL volumes. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 25°C. Immediately prior to use heat tubes in a boiling water bath for 10 min. Cool to 45°C. Aseptically add 1.0mL of sterile carbohydrate solution. Mix thoroughly.
Use: For the cultivation and differentiation of Clostridium perfringens based on carbohydrate fermentation patterns.
SPS Agar (Sulfite Polymyxin Sulfadiazine Agar Composition per liter: Pancreatic digest of casein................................15.0g Agar ..................................................................13.9g Yeast extract......................................................10.0g Ferric citrate........................................................0.5g Na2SO3 ................................................................0.5g Sulfadiazine ......................................................0.12g Polymyxin sulfate .............................................0.01g pH 7.0 ± 0.2 at 25°C
Source: This medium is available as a premixed
Preparation of Medium: Add components, ex-
powder from BD Diagnostic Systems.
cept glycerol, to distilled/deionized water and bring volume to 700.0mL. Mix thoroughly. Gently heat and bring to boiling. Add 300.0mL of glycerol. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 10 min at 11 psi pressure–116°C.
Preparation of Medium: Add components to
Use: For the preservation of viable microorganisms
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 13 psi pressure–118°C. Pour into sterile Petri dishes or leave in tubes.
in stool specimens. For the transport of fecal material.
Use: For the isolation and detection of Clostridium
Spray’s Fermentation Medium
SS Deoxycholate Agar (Salmonella-Shigella Deoxycholate Agar) (SSDC)
Composition per 1100.0mL: Neopeptone .......................................................10.0g Pancreatic digest of casein................................10.0g Agar ....................................................................2.0g Sodium thioglycolate ......................................0.025g Carbohydrate solution................................. 110.0mL pH 7.4 ± 0.1 at 25°C
Carbohydrate Solution: Composition per 200.0mL: Carbohydrate.....................................................20.0g
Preparation of Carbohydrate Solution: Add carbohydrate to distilled/deionized water and bring volume to 200.0mL. Glucose or glycerol may be used. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except agar and carbohydrate solution, to distilled/
perfringens and Clostridium botulinum.
Composition per liter: Agar ..................................................................13.5g Lactose..............................................................10.0g Sodium desoxycholate ......................................10.0g Bile salts..............................................................8.5g Na2S2O3 ..............................................................8.5g Sodium citrate.....................................................8.5g Beef extract.........................................................5.0g Pancreatic digest of casein..................................2.5g Peptic digest of animal tissue .............................2.5g CaCl2·2H2O ........................................................1.0g Ferric citrate........................................................1.0g
398
ST Holding Medium
Neutral Red .....................................................0.025g Brilliant Green ...............................................0.33mg pH 7.0 ± 0.2 at 25°C
70.0mL. Mix thoroughly. Adjust pH to 5.5 with 2N HCl. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Preparation of Medium: Add components to
Fresh Yeast Extract Solution: Composition per 100.0mL:
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Do not autoclave. Cool to 45°–50°C. Pour into sterile Petri dishes in 20.0mL volumes. Allow the surface of the plates to dry before inoculation.
Use: For the isolation and cultivation of Yersinia enterocolitica.
ST Holding Medium (m-ST Holding Medium) Composition per liter: KH2PO4 ...............................................................3.0g Tris(hydroxymethyl)aminomethane buffer.........3.0g Sulfanilamide ......................................................1.5g NaH2PO4·H2O.....................................................0.1g Ethanol (95% solution) ................................. 10.0mL pH 8.6 ± 0.2 at 25°C
Preparation of Medium: Dissolve the sulfanilamide in the ethanol. Add all components to distilled/ deionized water and bring volume to 1.0L. Mix thoroughly. Autoclave for 15 min at 15 psi pressure– 121°C. Distribute in 1.8mL volumes to sterile Petri dishes with tight-fitting lids and an absorbent filter.
Use: For the cultivation and enumeration of coliform bacteria by the delayed-incubation total coliform procedure. For use as a holding or transport medium to keep coliform bacteria viable between sampling and laboratory culture.
Baker’s yeast, live, pressed, starch-free,...........25.0g
Preparation of Fresh Yeast Extract Solution: Add the live Baker’s yeast to 100.0mL of distilled/ deionized water. Autoclave for 90 min at 15 psi pressure–121°C. Allow to stand. Remove supernatant solution. Adjust pH to 6.6–6.8. Penicillin Solution: Composition per 10.0mL: Penicillin G ............................................. 1,000,000U
Preparation of Penicillin Solution: Add penicillin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
CVA Enrichment: Composition per liter: Glucose ...........................................................100.0g L-Cysteine·HCl·H2O..........................................25.9g L-Glutamine ......................................................10.0g L-Cystine·2HCl ...................................................1.0g Adenine...............................................................1.0g Nicotinamide adenine dinucleotide ..................0.25g Cocarboxylase.....................................................0.1g Guanine·HCl .....................................................0.03g Fe(NO3)3 ...........................................................0.02g p-Aminobenzoic acid......................................0.013g Vitamin B12 .......................................................0.01g Thiamine·HCl ..................................................3.0mg
Preparation of CVA Enrichment: Add compo-
Standard Fluid Medium 10B (Shepard’s M10 Medium) Composition per 102.5mL: Base solution................................................. 70.0mL Horse serum, unheated.................................. 20.0mL Fresh yeast extract solution........................... 10.0mL Penicillin solution ........................................... 1.0mL CVA enrichment.............................................. 0.5mL L-Cysteine·HCl·H2O solution.......................... 0.5mL Urea solution................................................... 0.4mL Phenol Red...................................................... 0.1mL pH 6.0 ± 0.2 at 25°C
Base Solution: Composition per 70.0mL: Beef heart, solids from infusion..........................5.0g Peptone................................................................1.0g NaCl ....................................................................0.5g
nents to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize. L-Cysteine·HCl·H2O
Solution: Composition per 10.0mL: L-Cysteine·HCl·H2O ...........................................0.2g
Preparation of L-Cysteine·HCl·H2O Solution: Add L-cysteine·HCl·H2O to distilled/deionized
water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Urea Solution: Composition per 10.0mL: Urea.....................................................................1.0g
Preparation of Urea Solution: Add urea to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Base Solution: Add components
Phenol Red Solution: Composition per 10.0mL:
to distilled/deionized water and bring volume to
Phenol Red..........................................................0.1g
Staphylococcus Medium No. 110
399
Preparation of Phenol Red Solution: Add Phe-
Preparation of Medium: Add components to
nol Red to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C.
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes. Swirl flask while pouring plates to disperse precipitate.
Preparation of Medium: To 70.0mL of cooled, sterile base solution, aseptically add 20.0mL of sterile horse serum, 10.0mL of sterile fresh yeast extract solution, 1.0mL of sterile penicillin solution, 0.5mL of sterile CVA enrichment, 0.5mL of sterile L-cysteine·HCl·H2O solution, 0.4mL of sterile urea solution, and 0.1mL of sterile Phenol Red solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the isolation and cultivation of Ureaplasma urealyticum from clinical specimens.
Standard II Nutrient Agar Composition per liter: Agar ..................................................................13.0g Tryptose ..............................................................7.0g NaCl ....................................................................5.0g pH 7.5 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the isolation and enumeration of staphylococci from clinical and nonclinical specimens.
Staphylococcus Broth (m-Staphylococcus Broth) Composition per liter: NaCl..................................................................75.0g Mannitol............................................................10.0g Pancreatic digest of casein................................10.0g K2HPO4...............................................................5.0g Yeast extract........................................................2.5g Lactose................................................................2.0g pH 7.0 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation and enumeration of pathogenic and enterotoxigenic staphylococci by the membrane filter method.
Staphylococcus Medium
Use: For the cultivation of nonfastidious microor-
Composition per liter:
ganisms. For the maintenance of cultures of a wide variety of nonfastidious bacteria. May also be used as a base for blood and other enrichments for the cultivation of fastidious microorganisms. May be used to determine indole production.
Agar ..................................................................15.0g Peptone ...............................................................6.0g Pancreatic digest of casein..................................4.0g Yeast extract........................................................3.0g Beef extract.........................................................1.5g Glucose ...............................................................1.0g pH 6.6 ± 0.2 at 25°C
Staphylococcus Agar No. 110 Composition per liter: NaCl ..................................................................75.0g Gelatin...............................................................30.0g Agar ..................................................................15.0g D-Mannitol ........................................................10.0g Pancreatic digest of casein................................10.0g K2HPO4 ...............................................................5.0g Yeast extract........................................................2.5g Lactose ................................................................2.0g pH 7.0 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems and Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of Staphylococcus aureus. For the enumeration of pathogenic and enterotoxigenic staphylococci by the membrane filter method.
Staphylococcus Medium No. 110 Composition per liter: NaCl..................................................................75.0g
400
Staphylococcus/Streptococcus Selective Medium
Gelatin...............................................................30.0g Agar ..................................................................15.0g Mannitol............................................................10.0g Pancreatic digest of casein................................10.0g K2HPO4 ...............................................................5.0g Yeast extract........................................................2.5g Lactose ................................................................2.0g pH 7.1 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Mix thoroughly. Pour into sterile Petri dishes or leave in tubes.
Use: For the selective isolation, cultivation, and maintenance of Staphylococcus species.
Staphylococcus/Streptococcus Selective Medium Composition per 1060.0mL: Columbia blood agar base.................................. 1.0L Horse blood, defibrinated ............................. 50.0mL Antibiotic inhibitor ....................................... 10.0mL pH 7.3 ± 0.2 at 25°C
Columbia Blood Agar Base: Composition per liter: Special peptone .................................................23.0g Agar ..................................................................10.0g NaCl ....................................................................5.0g Starch ..................................................................1.0g
Source: Columbia blood agar base is available as a premixed powder from Oxoid Unipath. Preparation of Columbia Blood Agar Base: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Antibiotic Inhibitor: Composition per 10.0mL: Nalidixic acid ..................................................0.015g Colistin sulfate ..................................................0.01g Ethanol (95% solution) ................................. 10.0mL
Preparation of Antibiotic Inhibitor: Add components to 10.0mL ethanol. Mix thoroughly. Filter sterilize.
Preparation of Medium: To 1.0L of cooled sterile Columbia blood agar base, aseptically add sterile horse blood and sterile antibiotic inhibitor. Mix thor-
oughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the selective isolation of Staphylococcus aureus and streptococci from clinical specimens.
Starch Agar Composition per liter: Agar ..................................................................12.0g Soluble starch....................................................10.0g Beef extract.........................................................3.0g pH 7.5 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes.
Use: For the cultivation and differentiation of a variety of microorganisms based on amylase production. After incubation, starch hydrolysis is determined by the addition of Gram’s or Lugol’s iodine solution. Organisms that produce amylase appear as colonies surrounded by a clear zone.
Starch Agar with Bromcresol Purple Composition per liter: Agar ..................................................................15.0g Cornstarch.........................................................10.0g Meat peptone ....................................................10.0g Bromcresol Purple solution ............................ 1.2mL pH 6.8 ± 0.2 at 25°C
Bromcresol Purple Solution: Composition per 10.0mL: Bromcresol Purple ............................................0.16g Ethanol (95% solution) ................................. 10.0mL
Preparation of Bromcresol Purple Solution: Add Bromcresol Purple to 10.0mL of 95% ethanol. Mix thoroughly. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the differentiation of Gardnerella vaginalis (Haemophilus vaginalis, Corynebacterium vaginale) from other microorganisms found in the genitourinary tract, with the exception of some strains of Streptococcus and Loctobacillus. Differentiation is
Stock Culture Agar based on starch hydrolysis. Bacteria that can hydrolyze starch appear as colonies surrounded by a yellow zone.
Starch Agar with Bromcresol Purple Composition per liter: Solution 1.................................................... 200.0mL Solution 2...................................................... 20.0mL pH 7.8 ± 0.2 at 25°C
Solution 1: Composition per 200.0mL: Heart infusion agar.......................................... 5.0mL Bromcresol Purple solution ............................ 0.2mL
Preparation of Solution 1: Add components to distilled/deionized water and bring volume to 200.0mL. Mix thoroughly. Gently heat while stirring and bring to boiling.
Heart Infusion Agar: Composition per liter: Beef heart, solids from infusion......................500.0g Agar ..................................................................15.0g Tryptose ............................................................10.0g NaCl ....................................................................5.0g
Preparation of Heart Infusion Agar: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Bromcresol Purple Solution: Composition per 10.0mL: Bromcresol Purple ............................................0.16g Ethanol (95% solution) ................................. 10.0mL
Preparation of Bromcresol Purple Solution: Add Bromcresol Purple to 10.0mL of ethanol. Mix thoroughly.
401
lyze starch appear as colonies surrounded by a yellow zone.
Starch Hydrolysis Agar Composition per liter: Beef heart, infusion from................................500.0g Soluble starch....................................................20.0g Agar ..................................................................15.0g Tryptose ............................................................10.0g NaCl....................................................................5.0g pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and differentiation of a variety of microorganisms based on amylase production. After incubation, starch hydrolysis is determined by the addition of Gram’s or Lugol’s iodine solution. Organisms that produce amylase appear as colonies surrounded by a clear zone.
Sterility Test Broth (USP Alternative Thioglycolate Medium) Composition per liter: Pancreatic digest of casein................................15.0g Glucose ...............................................................5.0g Yeast extract........................................................5.0g NaCl....................................................................2.5g L-Cystine .............................................................0.5g Sodium thioglycolate ..........................................0.5g pH 7.1 ± 0.2 at 25°C
Solution 2: Composition per 20.0mL:
Source: This medium is available as a premixed
Starch ..................................................................0.4g
Preparation of Medium: Add components to
Preparation of Solution 2: Add starch to dis-
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C. If not used immediately, prior to inoculation heat tubes in a boiling water bath for 5–10 min. Cool to 25°C.
tilled/deionized water and bring volume to 20.0mL. Mix thoroughly. Gently heat while stirring and bring to boiling.
Preparation of Medium: Combine solution 1 and solution 2. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or distribute into sterile tubes. Use: For the differentiation of Gardnerella vaginalis (Haemophilus vaginalis, Corynebacterium vaginale) from other microorganisms found in the genitourinary tract, with the exception of some strains of Streptococcus and Lactobacillus. Differentiation is based on starch hydrolysis. Bacteria that can hydro-
powder from BD Diagnostic Systems.
Use: As an alternate medium, instead of fluid thioglycolate broth, for testing the sterility of a variety of specimens.
Stock Culture Agar Composition per liter: Beef heart infusion..........................................500.0g Gelatin...............................................................10.0g
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Stock Culture Agar with L-Asparagine
Proteose peptone ...............................................10.0g Agar ....................................................................7.5g Casein..................................................................5.0g Na2HPO4 .............................................................4.0g Sodium citrate .....................................................3.0g Glucose ...............................................................0.5g pH 7.5 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components to cold distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the maintenance of pathogenic and nonpathogenic bacteria, especially streptococci.
Stock Culture Agar with L-Asparagine Composition per liter: Beef heart infusion..........................................500.0g Gelatin...............................................................10.0g Proteose peptone ...............................................10.0g Agar ....................................................................7.5g Casein..................................................................5.0g Na2HPO4 .............................................................4.0g Sodium citrate .....................................................3.0g L-Asparagine .......................................................1.0g Glucose ...............................................................0.5g pH 7.5 ± 0.2 at 25°C
Preparation of Medium: Add components to cold distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the maintenance of pathogenic and nonpathogenic bacteria, especiallly streptococci.
Stonebrink’s Medium Composition per 1600.0mL: Homogenized whole egg ................................... 2.0L Mineral salts solution......................................... 1.0L Malachite Green solution.............................. 40.0mL
Mineral Salts Solution: Na-pyruvate ......................................................12.5g KH2PO4 ...............................................................7.0g Na2HPO4·7H2O...................................................4.0g
volume to 1.0L. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C.
Malchite Green Solution: Composition per 100.0mL: Malachite green ..................................................2.0g
Preparation of Malchite Green Solution: Add malachite to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C. Homogenized Whole Egg: Composition per 2.0L: Whole eggs ...................................................... 36-48
Preparation of Homogenized Whole Egg: Use fresh eggs, less than 1 week old. Scrub the shells with soap. Let stand in a soap solution for 30 min. Rinse in running water. Soak eggs in 70% ethanol for 15 min. Break the eggs into a sterile container. Homogenize by shaking. Filter through four layers of sterile cheesecloth into a sterile graduated cylinder. Measure out 2.0L. Preparation of Medium: Aseptically add 40.0mL sterile malachite to 1.0L of sterile mineral salts solution. Mix thoroughly. Aseptically add 2.0L of homogenized whole egg. Mix thoroughly. Distribute into sterile screw-capped tubes. Place tubes in a slanted position. Inspissate at 85°C (moist heat) for 45 min. Use: For the cultivation of Mycobacterium species. For the isolation of Mycobacterium bovis.
Strep ID Quad Plate Composition per liter: Quadrant I ....................................................... 5.0mL Quadrant II...................................................... 5.0mL Quadrant III .................................................... 5.0mL Quadrant IV .................................................... 5.0mL
Source: Available as a prepared medium from BD Diagnostic Systems.
Quadrant I: Composition per 5.0mL: Bacitracin.........................................................0.5mg TSA II agar ..................................................... 5.0mL
Quadrant II: Composition per 5.0mL: TSA II agar ..................................................... 5.0mL Sheep blood, defibrinated ............................. 0.25mL
Quadrant III: Composition per 5.0mL: Bile esculin agar ............................................. 5.0mL
Preparation of Mineral Salts Solution: Add
Quadrant IV: Composition per 5.0mL:
components to distilled/deionized water and bring
Blood agar base with 6.5% NaCl.................... 5.0mL
Streptococcus Blood Agar, Selective Preparation of Quadrant Media: Sterilize agars by autoclaving for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C. Add additional components as filter sterilized solutions. Mix and distribute as 5.0mL aliquots into quadrants. Use: For the differentiation and presumptive identification of streptococci. The Strep (Streptococcus) ID (Identification) Quad Plate is a four-sectored plate, each containing a different medium.
StrepB Carrot Broth™
403
Preparation of Bromcresol Purple Solution: Add Bromcresol Purple to 10.0mL of ethanol. Mix thoroughly. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes in 5.0mL volumes. Autoclave for 15 min at 15 psi pressure– 121°C.
Use: For the cultivation of Streptococcus species and other Gram-positive cocci. Growth in this medium turns the indicator yellow and the solution turbid.
Composition per liter: Proteose peptone no. 3 ......................................25.0g Soluble starch....................................................20.0g MgSO4 ..............................................................20.0g Selective agents.................................................12.2g Morpholinepropanesulfonic acid (MOPS)........11.0g Na2HPO4 .............................................................8.5g Glucose ...............................................................2.5g Sodium Pyruvate.................................................1.0g StrepB carrot broth disk growth promoting factors ...................................variable pH 7.4 ± 0.1 at 25°C
Source: This medium is available from Hardy Diagnostics.
Preparation: This medium is supplied as a prepared broth in tubes. The StrepB carrot broth disk is added to a tube just prior to inoculation with a vaginal swab. The disk must remain submerged in the broth.
Use: For detecting the presence of Group B Streptococcus infections in pregnant women. This new screening test is an improvement over conventional methods, by increasing sensitivity, decreasing turn around time, while lowering overall cost. Tubes show an orange to red color change, typical of group B streptococci.
Streptococcal Growth Medium Composition per liter:
Streptococcus Agar Composition per liter: Glucose .............................................................20.0g Pancreatic digest of casein................................20.0g Agar ..................................................................15.0g K2HPO4...............................................................2.0g MgSO4·7H2O ......................................................0.1g pH 6.8 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of Streptococcus species.
Streptococcus Blood Agar, Selective Composition per liter: Agar ..................................................................15.0g Pancreatic digest of casein................................10.0g Beef extract.........................................................6.7g Nucleic acid ........................................................6.0g NaCl....................................................................5.0g Sheep blood, defibrinated ............................. 50.0mL Maltose solution............................................ 10.0mL Antibiotic inhibitor ....................................... 10.0mL pH 7.3 ± 0.2 at 25°C
Maltose Solution: Composition per 10.0mL:
Beef heart, solids from infusion......................500.0g Tryptose ............................................................10.0g NaCl ....................................................................5.0g Glucose ...............................................................1.0g Bromcresol Purple solution ............................ 1.0mL pH 7.4 ± 0.2 at 25°C
Preparation of Maltose Solution: Add maltose to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Bromcresol Purple Solution: Composition per 10.0mL:
Antibiotic Inhibitor: Composition per 10.0mL:
Bromcresol Purple ............................................0.16g Ethanol (95% solution) ................................. 10.0mL
Polymyxin B sulfate .........................................0.02g Neomycin sulfate ..............................................0.01g
Maltose ......................................................0.25–5.0g
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Streptococcus Medium
Preparation of Antibiotic Inhibitor: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components—except sheep blood, maltose solution, and antibiotic inhibitor—to distilled/deionized water and bring volume to 930.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile sheep blood, sterile maltose solution, and sterile antibiotic inhibitor. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation and cultivation of group A hemolytic Streptococcus species from the human respiratory tract.
Streptococcus Medium Composition per liter: Agar ..................................................................15.0g Glucose ...............................................................4.0g K2HPO4 ...............................................................3.8g Pancreatic digest of casein..................................2.5g Yeast extract........................................................2.5g pH 7.6 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of Enterococcus faecalis.
Streptococcus pneumoniae Medium Composition per liter: Pancreatic digest of casein................................17.0g Glucose .............................................................10.0g NaCl ....................................................................5.0g Papaic digest of soybean meal ............................3.0g Yeast extract........................................................3.0g K2HPO4 ..............................................................2.5g pH 7.2 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.2. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of Streptococcus pneumoniae.
Streptococcus Selective Medium Composition per liter: Special peptone .................................................23.0g
Agar ..................................................................10.0g NaCl....................................................................5.0g Starch ..................................................................1.0g Horse blood, defibrinated ............................. 50.0mL Antibiotic inhibitor ....................................... 10.0mL pH 7.3± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath.
Antibiotic Inhibitor: Composition per 10.0mL: Colistin sulfate ...............................................10.0mg Oxolinic acid....................................................5.0mg
Preparation of Antibiotic Inhibitor: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except horse blood and antibiotic inhibitor, to distilled/ deionized water and bring volume to 940.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile horse blood and sterile antibiotic inhibitor. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the selective isolation of streptococci from clinical specimens.
Streptosel™ Agar Composition per liter: Pancreatic digest of casein................................15.0g Agar ..................................................................12.0g Glucose ...............................................................5.0g Papaic digest of soybean meal............................5.0g NaCl....................................................................4.0g Sodium citrate.....................................................1.0g L-Cystine .............................................................0.2g NaN3 ...................................................................0.2g Na2SO3 ................................................................0.2g Crystal Violet ...................................................0.2mg pH 7.4 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. If medium is used the same day, do not autoclave. Pour into sterile Petri dishes or leave in tubes. If medium is to be stored, autoclave for 15 min at 13 psi pressure–118°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the selective isolation, cultivation, and enumeration of streptococci from specimens containing a mixed flora.
Stuart Transport Medium, Modified
Streptosel Broth Composition per liter: Pancreatic digest of casein................................15.0g Glucose ...............................................................5.0g Papaic digest of soybean meal ............................5.0g NaCl ....................................................................4.0g Sodium citrate .....................................................1.0g L-Cystine .............................................................0.2g Na2SO3 ................................................................0.2g NaN3 ...................................................................0.2g Crystal Violet ...................................................0.2mg pH 7.4 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 13 psi pressure–118°C.
Use: For the selective isolation and cultivation of streptococci from specimens containing a mixed flora.
Stuart Leptospira Broth, Modified Composition per liter: NaCl ..................................................................1.93g Na2HPO4 ...........................................................0.66g NH4Cl ...............................................................0.34g MgCl2·6H2O .....................................................0.19g L-Asparagine .....................................................0.13g KH2PO4 .............................................................0.08g Rabbit serum, inactivated at 56°C, 30 min .................. 100.0mL Glycerol .......................................................... 5.0mL pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add each component, except rabbit serum, to distilled/deionized water in separate flasks and bring each volume to 100.0mL. Mix thoroughly. Combine the seven solutions, except the rabbit serum. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile rabbit serum. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation of Leptospira species.
Stuart Medium Base Composition per 1100.0mL: NaCl ....................................................................1.8g Na2HPO4 ...........................................................0.67g MgCl2·6H2O .....................................................0.41g NH4Cl ...............................................................0.27g Asparagine ........................................................0.13g KH2PO4 .............................................................0.09g
405
Phenol Red........................................................0.01g Leptospira enrichment ................................ 100.0mL Glycerol .......................................................... 5.0mL pH 7.6 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Leptospira enrichment contains rabbit serum and hemoglobin and is available from BD Diagnostic Systems.
Preparation of Medium: Add components, except glycerol and Leptospira enrichment, to distilled/ deionized water and bring volume to 995.0mL. Mix thoroughly. Add glycerol. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add Leptospira enrichment. Mix thoroughly. Aseptically distribute into sterile screw-capped tubes in 10.0mL volumes.
Use: For the cultivation of Leptospira species.
Stuart Transport Medium Composition per liter: Sodium glycerophosphate.................................10.0g Sodium thioglycolate ..........................................1.0g CaCl2·2H2O ........................................................0.1g Methylene Blue................................................2.0mg pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into 7.0mL screw-capped tubes. Fill tubes to capacity. Autoclave for 15 min at 15 psi pressure– 121°C.
Use: For the preservation of Neisseria species and other fastidious organisms during their transport from clinic to laboratory.
Stuart Transport Medium, Modified Composition per liter: Sodium glycerophosphate.................................10.0g Agar ....................................................................5.0g L-Cysteine·HCl·H2O ...........................................0.5g Sodium thioglycolate ..........................................0.5g CaCl2·2H2O ........................................................0.1g Methylene Blue................................................1.0mg pH 7.4 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into 7.0mL screw-capped tubes. Fill tubes to capacity. Autoclave for 15 min at 15 psi pressure–121°C.
406
Sucrose Phosphate Glutamate Transport Medium
Use: For the preservation of Neisseria species and other fastidious organisms during their transport from clinic to laboratory.
Sucrose Phosphate Glutamate Transport Medium Composition per liter: Sucrose..............................................................75.0g Na2HPO4 ...........................................................1.22g Glutamic acid ....................................................0.72g K2HPO4 .............................................................0.52g Bovine serum ................................................ 50.0mL Antibiotic inhibitor ....................................... 10.0mL pH 7.4–7.6 at 25°C
Antibiotic Inhibitor: Composition per 10.0mL: Vancomycin ........................................................0.1g Streptomycin .....................................................0.05g Nystatin.........................................................25000U
Preparation of Antibiotic Inhibitor: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except bovine serum and antibiotic inhibitor, to distilled/deionized water and bring volume to 940.0mL. Mix thoroughly. Gently heat and bring to boiling. Adjust pH to 7.4–7.6. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile bovine serum and sterile antibiotic inhibitor. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
ized water and bring volume to 940.0mL. Mix thoroughly. Gently heat and bring to boiling. Adjust pH to 7.0. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile bovine serum and sterile antibiotic inhibitor. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the maintenance of Chlamydia species during transport.
Sucrose Teepol Tellurite Agar (STT Agar) Composition per liter: Agar ..................................................................20.0g Beef extract.........................................................1.0g Peptone ...............................................................1.0g Sucrose................................................................1.0g NaCl....................................................................0.5g Bromthymol Blue (0.2% solution) ................. 2.5mL Tellurite solution ............................................. 2.5mL Sodium lauryl sulfate (Teepol, 0.1% solution) ............................ 0.2mL pH 8.0 ± 0.2 at 25°C
Tellurite Solution: Composition per 100.0mL: K2TeO3 ..............................................................0.05g
Preparation of Tellurite Solution: Add the K2TeO3 to distilled/deionized water and bring the volume to 100.0mL. Mix thoroughly. Filter sterilize. Use freshly prepared solution.
Caution: Potassium tellurite is toxic.
Use: For the maintenance of Chlamydia species dur-
Preparation of Medium: Add components to
ing transport.
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Do not autoclave. Pour into sterile Petri dishes.
Sucrose Phosphate Transport Medium Composition per liter:
Use: For the selective isolation, cultivation, and dif-
Sucrose..............................................................68.5g K2HPO4 ...............................................................2.1g KH2PO4 ...............................................................1.1g Bovine serum ................................................ 50.0mL Antibiotic inhibitor ....................................... 10.0mL pH 7.0 ± 0.2 at 25°C
ferentiation of Vibrio species based on their ability to ferment sucrose. Vibrio cholerae appears as flat yellow colonies. Vibrio parahaemolyticus appears as elevated green-yellow mucoid colonies.
Antibiotic Inhibitor: Composition per 10.0mL:
Composition per liter:
Vancomycin ........................................................0.1g Streptomycin .....................................................0.05g Nystatin........................................................25,000U
Preparation of Antibiotic Inhibitor: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Sucrose Yeast Extract Medium Sucrose..............................................................20.0g Yeast extract........................................................4.0g K2HPO4...............................................................2.5g MgSO4·7H2O ......................................................1.0g Trace elements solution .................................. 4.0mL pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Add components, except
Trace Elements Solution: Composition per liter:
bovine serum and antibiotic inhibitor, to distilled/deion-
ZnSO4·7H2O .....................................................18.0g
TCBS Agar FeSO4·7H2O........................................................9.0g MnSO4·4H2O ......................................................3.0g CoCl2·6H2O ........................................................0.9g CuSO4·5H2O .......................................................0.8g Conc. H2SO4 ................................................... 5.0mL
Preparation of Trace Elements Solution: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of a variety of bacteria that can utilize sucrose as carbon source.
Tap Water Agar
407
KH2PO4........................................................... 0.117g NaNO3 ............................................................0.085g pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the differentiation of Mycobacterium species based on nitrate reduction. After growth of cells in appropriate medium, nitrate reduction is determined by making a suspension of cells in TB nitrate reduction broth and adding hydrochloric acid, sulfanilamide, and N-naphylenendiamine. Nitrate reduction turns the medium pink. Mycobacterium tuberculosis reduces nitrate and turns the medium deep pink within 1 min. Mycobacterium bovis does not reduce nitrate and does not change the medium.
Composition per liter: Agar ..................................................................15.0g Tap water............................................................ 1.0L
Preparation of Medium: Add agar to 1.0L of tap water. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes.
Use: For the cultivation and differentiation of fungi and aerobic actinomycetes based on filament and aerial hyphae morphology.
Tarshis Blood Agar Composition per 1050.0mL: Beef heart infusion..........................................500.0g Agar ..................................................................15.0g Meat peptone.....................................................10.0g NaCl ....................................................................5.0g Penicillin G, sterile .....................................100,000U Sheep blood, sterile..................................... 300.0mL Glycerol ........................................................ 10.0mL pH 6.6 ± 0.2 at 25°C
Preparation of Medium: Add components, except sheep blood and penicillin G, to distilled/deionized water and bring volume to 750.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile sheep blood and sterile penicillin G. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation and cultivation of Mycobacterium tuberculosis.
TB Nitrate Reduction Broth Composition per 100.0mL: Na2HPO4·12H2O.............................................0.485g
TBX Agar (Tryptone Bile X-glucuronide Agar) Composition per liter: Peptone .............................................................20.0g Agar ..................................................................15.0g Bile salts..............................................................1.5g X-β-D-glucuronide..........................................0.075g pH 7.2 ± 0.2 at 25°C
Source: This medium is available from Fluka, Sigma-Aldrich.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Pour into sterile Petri dishes.
Use: For the detection and enumeration of E. coli without further confirmation. E. coli colonies are colored blue-green. The presence of the enzyme β-Dglucuronidase differentiates most E. coli ssp. from other coliforms. E. coli absorbs the chromogenic substrate 5-bromo-4-chloro-3-indolyl-β-D-glucuronide. The enzyme β-glucuronidase splits the bond between the chromophore 5-bromo-4-chloro-3-indolyle- and the β-D-glucuronide. E. coli colonies are colored blue-green. Growth of accompanying Grampositive flora is largely inhibited by the use of bile salts.
TCBS Agar (Thiosulfate Citrate Bile Salt Sucrose Agar) Composition per liter: Sucrose..............................................................20.0g Agar ..................................................................14.0g
408
TCH Medium
NaCl ..................................................................10.0g Sodium citrate ...................................................10.0g Na2S2O3 ............................................................10.0g Yeast extract........................................................5.0g Pancreatic digest of casein..................................5.0g Peptic digest of animal tissue..............................5.0g Oxgall..................................................................5.0g Sodium cholate ...................................................3.0g Ferric citrate........................................................1.0g Thymol Blue .....................................................0.04g Bromthymol Blue .............................................0.04g pH 8.6 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Do not autoclave. Cool to 45°–50°C. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the selective isolation of Vibrio cholerae and Vibrio parahaemolyticus from a variety of clinical and nonclinical specimens.
TCH Medium (Thiophene 2 Carboxylic Acid Hydrazide Medium)
Middlebrook OADC Enrichment: Composition per 100.0mL: Bovine albumin fraction V .................................5.0g Glucose ...............................................................2.0g NaCl..................................................................0.85g Oleic acid ..........................................................0.05g Catalase............................................................4.0mg
Source: This enrichment is available as a prepared enrichment from BD Diagnostic Systems. Preparation of Middlebrook OADC Enrichment: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation for Medium: Combine components. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the differentiation of Mycobacterium species based on sensitivity to TCH. Mycobacterium bovis is inhibited by TCH. Mycobacterium tuberculosis and other mycobacteria are generally resistant to low concentrations of TCH. This distinguishes Mycobacterium bovis from other nonchromogenic, slowgrowing mycobacteria.
Tellurite Glycine Agar
Composition per 1105.0mL:
Composition per liter:
Thiophene-2-carboxylic acid hydrazide ..........1.1mg Middlebrook 7H10 agar base............................. 1.0L OADC enrichment ...................................... 100.0mL Glycerol .......................................................... 5.0mL pH 6.6 ± 0.2 at 25°C
Agar ..................................................................17.5g Pancreatic digest of casein................................10.0g Glycine..............................................................10.0g Yeast extract........................................................6.5g D-Mannitol ..........................................................5.0g K2HPO4...............................................................5.0g LiCl .....................................................................5.0g Enzymatic hydrolysate of soybean meal ............3.5g Chapman tellurite solution............................ 10.0mL pH 7.2 ± 0.2 at 25°C
Middlebrook 7H10 Agar Base: Composition per liter: Agar ..................................................................15.0g Na2HPO4 .............................................................1.5g KH2PO4 ...............................................................1.5g (NH4)2SO4...........................................................0.5g L-Glutamic acid ...................................................0.5g Sodium citrate .....................................................0.4g Ferric ammonium citrate...................................0.04g MgSO4·7H2O ..................................................0.025g ZnSO4·7H2O ....................................................1.0mg CuSO4·5H2O ....................................................1.0mg Pyridoxine........................................................1.0mg Biotin ...............................................................0.5mg CaCl2·2H2O......................................................0.5mg Malachite Green.............................................0.25mg
Preparation of Middlebrook 7H10 Agar Base: Add glycerol to 900.0mL of distilled/deionized water and add remaining components. Mix thoroughly. Gently heat and bring to boiling.
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Chapman Tellurite Solution: Composition per 100.0mL: K2TeO3 ................................................................1.0g
Preparation of Chapman Tellurite Solution: Add K2TeO3 to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Caution: Potassium tellurite is toxic. Preparation of Medium: Add components, except Chapman tellurite solution, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Asepti-
Tergitol 7 Agar
409
cally add 10.0mL of sterile Chapman tellurite solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes. Allow the surface of the plates to dry before inoculating.
Source: This medium is available as a premixed
Use: For the isolation and cultivation of coagulasepositive staphylococci.
Triphenyltetrazolium chloride ..........................0.05g
Tellurite Glycine Agar Composition per liter: Agar ..................................................................16.0g Pancreatic digest of casein................................10.0g Glycine..............................................................10.0g Yeast extract........................................................5.0g D-Mannitol ..........................................................5.0g K2HPO4 ...............................................................5.0g LiCl .....................................................................5.0g Chapman tellurite solution............................ 20.0mL pH 7.2 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Chapman Tellurite Solution: Composition per 100.0mL: K2TeO3 ................................................................1.0g
Preparation of Chapman Tellurite Solution: Add K2TeO3 to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Caution: Potassium tellurite is toxic. Preparation of Medium: Add components, except Chapman tellurite solution, to distilled/deionized water and bring volume to 980.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Aseptically add 20.0mL of sterile Chapman tellurite solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes. Allow the surface of the plates to dry before inoculating.
powder from Oxoid Unipath.
TTC Solution: Composition per 100.0mL: Preparation of TTC Solution: Add triphenyltetrazolium chloride to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 995.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 50°C. Aseptically add 5.0mL of sterile TTC solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the detection and enumeration of coliforms. Lactose-fermenting bacteria appear as yellow colonies. Lactose-nonfermenting bacteria appear as blue colonies.
Tergitol 7 Agar Composition per liter: Agar ..................................................................15.0g Lactose..............................................................10.0g Yeast extract........................................................3.0g Pancreatic digest of casein..................................2.5g Peptic digest of animal tissue .............................2.5g Tergitol 7.............................................................0.1g Bromthymol Blue ..........................................25.0mg TTC solution................................................... 3.0mL pH 6.9 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
TTC Solution: Composition per 100.0mL:
Use: For the quantitative detection of coagulase-
Triphenyltetrazolium chloride ............................1.0g
positive Staphyloccous species.
Preparation of TTC Solution: Add triphenyltet-
Tergitol 7 Agar Composition per liter: Lactose ..............................................................20.0g Agar ..................................................................13.0g Peptone..............................................................10.0g Yeast extract........................................................6.0g Meat extract ........................................................5.0g Tergitol-7.............................................................0.1g Bromthymol Blue .............................................0.05g TTC solution ................................................... 5.0mL pH 7.2 ± 0.2 at 25°C
razolium chloride to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 997.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 50°C. Aseptically add 3.0mL of sterile TTC solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the selective isolation and differentiation of coliform bacteria based on lactose fermentation. Lactose-
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Tergitol 7 Agar H
fermenting bacteria appear as yellow colonies. Lactosenonfermenting bacteria appear as blue colonies.
Tergitol 7 Agar H Composition per liter: Agar ..................................................................15.0g Lactose ..............................................................10.0g Yeast extract........................................................3.0g Pancreatic digest of casein..................................2.5g Peptic digest of animal tissue..............................2.5g Ferric ammonium citrate.....................................0.5g Na2S2O3 ..............................................................0.5g Tergitol 7 .............................................................0.1g Bromthymol Blue ...........................................0.025g pH 7.2 ± 0.2
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the selective isolation and differentiation of enteric bacteria from urine.
Tergitol 7 Broth Composition per liter:
Tetrathionate Broth Composition per liter: Na2S2O3 ............................................................40.7g CaCO3 ...............................................................25.0g NaCl....................................................................4.5g Peptone ...............................................................4.5g Yeast extract........................................................1.8g Beef extract.........................................................0.9g Iodine solution .............................................. 20.0mL
Iodine Solution: Composition per 20.0mL: Iodine ..................................................................6.0g KI ........................................................................5.0g
Preparation of Iodine Solution: Add iodine and KI to distilled/deionized water and bring volume to 20.0mL. Mix thoroughly.
Preparation of Medium: Add components, except iodine solution, to distilled/deionized water and bring volume to 980.0mL. Mix thoroughly. Gently heat and bring to boiling. Do not autoclave. Cool to 40°C. Add 20.0mL of iodine solution. Mix thoroughly. Distribute into tubes in 10.0mL volumes. Use medium the same day it is prepared.
Use: For the selective isolation and enrichment of Salmonella typhi and other salmonellae from fecal specimens.
Lactose ..............................................................10.0g Yeast extract........................................................3.0g Pancreatic digest of casein..................................2.5g Peptic digest of animal tissue..............................2.5g Tergitol 7 .............................................................0.1g Bromthymol Blue ..........................................25.0mg TTC solution ................................................... 3.0mL pH 6.9 ± 0.2 at 25°C
Composition per 1030.0mL:
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Tetrathionate Broth Base: Composition per liter:
TTC Solution: Composition per 100.0mL:
Na2S2O3·5H2O ..................................................30.0g CaCO3 ...............................................................10.0g Polypeptone ........................................................5.0g Bile salts..............................................................1.0g
Triphenyltetrazolium chloride ............................1.0g
Preparation of TTC Solution: Add triphenyltetrazolium chloride to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 997.0mL. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C. Aseptically add 3.0mL of sterile TTC solution. Mix thoroughly.
Use: For the isolation and cultivation of coliforms, Salmonella, and other enteric bacteria.
Tetrathionate Broth (FDA M145) Tetrathionate broth base..................................... 1.0L Iodine-potassium iodide solution.................. 20.0mL Brilliant Green solution ................................ 10.0mL pH 8.4 ± 0.2 at 25°C
Preparation of Tetrathionate Broth Base: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. A slight precipitate will remain. Do not autoclave. Cool to 25°C. Store at 4°C.
Iodine–Potassium Iodide Solution: Composition per 20.0mL: Iodine, resublimed ..............................................6.0g KI ........................................................................5.0g
Preparation of Iodine–Potassium Iodide Solution: Add KI to 5.0mL of sterile distilled/deion-
Tetrathionate Broth ized water. Mix thoroughly. Add iodine. Mix thoroughly. Bring volume to 20.0mL with sterile distilled/deionized water.
Brilliant Green Solution: Composition per 100.0mL: Brilliant Green ....................................................0.1g
Preparation of Brilliant Green Solution: Add Brilliant Green to sterile distilled/deionized water. Mix thoroughly.
Preparation of Medium: Combine 1.0L of tetrathionate broth base, 20.0mL of iodine-potassium iodide solution, and 10.0mL of Brilliant Green solution. Mix thoroughly. Aseptically distribute into tubes in 10.0mL volumes. Do not heat medium after it has been mixed.
Use: For the selective isolation and cultivation of Salmonella species.
Tetrathionate Broth (TT Broth) Composition per liter: Na2S2O3 ............................................................30.0g CaCO3 ...............................................................10.0g Proteose peptone .................................................5.0g
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Tetrathionate Broth (m-Tetrathionate Broth) (m-TT Broth) Composition per liter: Na2S2O3 ............................................................30.0g CaCO3 ...............................................................10.0g Pancreatic digest of casein..................................2.5g Peptic digest of animal tissue .............................2.5g Iodine-iodide solution................................... 20.0mL pH 8.0 ± 0.2 at 25°C
Iodine-Iodide Solution: Composition per 20.0mL: Iodine ..................................................................6.0g KI ........................................................................5.0g
Preparation of Iodine-Iodide Solution: Add iodine and KI to distilled/deionized water and bring volume to 20.0mL. Mix thoroughly.
Preparation of Medium: Add components, except iodine-iodide solution, to distilled/deionized water and bring volume to 980.0mL. Mix thoroughly. Gently heat and bring to boiling. Do not autoclave. Cool to 40°C. Add 20.0mL of iodine-iodide solution. Mix thoroughly. Distribute into tubes in 10.0mL volumes. Use medium the same day it is prepared.
Use: For the selective isolation in the membrane filter method of Salmonella species from feces, urine, and other specimens.
Bile salts..............................................................1.0g Iodine solution .............................................. 20.0mL pH 8.4± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Iodine Solution: Composition per 20.0mL: Iodine ..................................................................6.0g KI ........................................................................5.0g
Preparation of Iodine Solution: Add iodine and KI to distilled/deionized water and bring volume to 20.0mL. Mix thoroughly.
Preparation of Medium: Add components, except iodine solution, to distilled/deionized water and bring volume to 980.0mL. Mix thoroughly. Gently heat and bring to boiling. Do not autoclave. Cool to 40°C. Add 20.0mL of iodine solution. Mix thoroughly. Distribute into tubes in 10.0mL volumes. Use medium the same day it is prepared.
Use: For the selective isolation and enrichment of Salmonella typhi and other salmonellae from infectious material.
Tetrathionate Broth (m-Tetrathionate Broth) Composition per liter: Na2S2O3 ............................................................30.0g Proteose peptone.................................................5.0g Bile salts..............................................................1.0g Iodine solution .............................................. 20.0mL pH 8.0 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Iodine Solution: Composition per 20.0mL: Iodine ..................................................................6.0g KI ........................................................................5.0g
Preparation of Iodine Solution: Add iodine and KI to distilled/deionized water and bring volume to 20.0mL. Mix thoroughly.
Preparation of Medium: Add components, except iodine solution, to distilled/deionized water and bring volume to 980.0mL. Mix thoroughly. Gently heat and bring to boiling. Do not autoclave. Cool to 40°C. Add 20.0mL of iodine solution. Mix thoroughly. Use medium the same day it is prepared.
412
Tetrathionate Broth, Hajna
Use: For the enrichment of Salmonella species in the membrane filter method prior to placing the filter on selective media such as Brilliant Green broth.
Tetrathionate Broth, Hajna (TT Broth, Hajna) Composition per liter: Na2S2O3 ............................................................38.0g CaCO3 ...............................................................25.0g Casein/meat peptone (50/50) ............................18.0g NaCl ....................................................................5.0g D-Mannitol ..........................................................2.5g Yeast extract........................................................2.0g Glucose ...............................................................0.5g Sodium deoxycholate..........................................0.5g Brilliant Green ..................................................0.01g Iodine solution .............................................. 40.0mL pH 7.5–7.8 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Iodine Solution: Composition per 40.0mL: KI ........................................................................8.0g Iodine ..................................................................5.0g
Preparation of Iodine Solution: Add iodine and KI to distilled/deionized water and bring volume to 40.0mL. Mix thoroughly.
Preparation of Medium: Add components, except iodine solution, to distilled/deionized water and bring volume to 960.0mL. Mix thoroughly. Gently heat and bring to boiling. Do not autoclave. Cool to 40°C. Add 40.0mL of iodine solution. Mix thoroughly. Distribute into tubes in 10.0mL volumes. Use medium the same day it is prepared.
Use: For the isolation of Salmonella species, except Salmonella typhi, and Arizona species from fecal specimens, urine, and other specimens.
Tetrathionate Broth with Novobiocin Composition per liter: Na2S2O3 ............................................................38.0g CaCO3 ...............................................................25.0g Casein/meat peptone (50/50) ............................18.0g NaCl ....................................................................5.0g Yeast extract........................................................2.0g D-Mannitol ..........................................................0.5g Glucose ...............................................................0.5g Sodium deoxycholate..........................................0.5g Brilliant Green ..................................................0.01g Novobiocin.......................................................4.0mg Iodine solution .............................................. 40.0mL pH 7.5–7.8 at 25°C
Iodine Solution: Composition per 40.0mL: KI ........................................................................8.0g Iodine ..................................................................5.0g
Preparation of Iodine Solution: Add iodine and KI to distilled/deionized water and bring volume to 20.0mL. Mix thoroughly.
Preparation of Medium: Add components, except iodine solution, to distilled/deionized water and bring volume to 960.0mL. Mix thoroughly. Gently heat and bring to boiling. Do not autoclave. Cool to 40°C. Add 40.0mL of iodine solution. Mix thoroughly. Distribute into tubes in 10.0mL volumes. Use medium the same day it is prepared.
Use: For the isolation of Salmonella species, except Salmonella typhi, and Arizona species from fecal specimens. Novobiocin suppresses the growth of Proteus species.
Tetrathionate Broth, USA (TT Broth, USA) Na2S2O3 ............................................................30.0g CaCO3 ...............................................................10.0g Casein peptone....................................................2.5g Meat peptone ......................................................2.5g Bile salts..............................................................1.0g
Source: This medium is available as a premixed powder from Oxoid Unipath.
Iodine-Iodide Solution: Composition per 20.0mL: Iodine ..................................................................6.0g KI ........................................................................5.0g
Preparation of Iodine-Iodide Solution: Add iodine and KI to distilled/deionized water and bring volume to 20.0mL. Mix thoroughly.
Preparation of Medium: Add components, except iodine solution, to distilled/deionized water and bring volume to 980.0mL. Mix thoroughly. Gently heat and bring to boiling. Do not autoclave. Cool to 40°C. Add 20.0mL of iodine solution. Mix thoroughly. Distribute into tubes in 10.0mL volumes. Use medium the same day it is prepared.
Use: For the selective enrichment of Salmonella species from feces, urine, and other specimens.
Tetrathionate Crystal Violet Enhancement Broth Composition per liter: Potassium tetrathionate.....................................20.0g Casein/meat peptone (50/50) ..............................8.6g
Thayer-Martin Agar, Modified
413
NaCl ....................................................................6.4g Crystal Violet ..................................................0.005g pH 6.5 ± 0.2 at 25°C
Preparation of Glucose Solution: Add glucose to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components to
Thallous Acetate Solution: Composition per 10.0mL:
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the isolation of Salmonella species, except Salmonella typhi, and Arizona species from fecal specimens, urine, and other specimens.
Tetrathionate Reductase Test Medium Composition per 1025.0mL: K2S4O6 ................................................................5.0g Peptone water..................................................... 1.0L Bromthymol Blue (0.2% solution)................ 25.0mL pH 7.4 ± 0.2 at 25°C
Peptone Water: Composition per liter: Peptone..............................................................10.0g NaCl ....................................................................5.0g
Thallous acetate ..................................................1.0g
Preparation of Thallous Acetate Solution: Add thallous acetate to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components—except glucose solution, 2,3,5-triphenyltetrazolium·HCl solution, and thallous acetate solution—to distilled/ deionized water and bring volume to 880.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile glucose solution, 2,3,5-triphenyltetrazolium·HCl solution, and thallous acetate solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation of Streptococcus species.
Preparation of Peptone Water: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly.
Preparation of Medium: Combine components. Mix thoroughly. Adjust pH to 7.4. Filter sterilize. Dispense into tubes in 1.0mL volumes or into wells of sterile microculture plates for replica inoculation.
Use: For the cultivation and identification of Serratia species based on their ability to reduce tetrathionate. Bacteria that reduce tetrathionate turn the medium yellow.
Tetrazolium Thallium Glucose Agar Composition per liter: Agar ..................................................................14.0g Beef extract .......................................................10.0g Peptone..............................................................10.0g Glucose solution ......................................... 100.0mL 2,3,5-Triphenyltetrazolium·HCl solution...... 10.0mL Thallous acetate solution .............................. 10.0mL
2,3,5-Triphenyltetrazolium·HCl Solution: Composition per 10.0mL: 2,3,5-Triphenyltetrazolium·HCl..........................0.1g
Preparation of 2,3,5-TriphenyltetrazoliumHCl Solution: Add 2,3,5-triphenyltetrazolium·HCl to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Autoclave for 7 min at 15 psi pressure–121°C.
Glucose Solution: Composition per 100.0mL: Glucose .............................................................10.0g
Tetrazolium Tolerance Agar (TTC Agar) Composition per liter: Pancreatic digest of casein................................15.0g Agar ..................................................................15.0g Triphenyltetrazolium chloride ..........................10.0g Papaic digest of soybean meal............................5.0g NaCl....................................................................5.0g pH 7.3 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Do not overheat. Pour into sterile Petri dishes or leave in tubes.
Use: For the differentiation of bacteria based upon the ability to tolerate and grow in the presence of tetrazolium. Streptococcus faecalis (enterococci) rapidly reduces tetrazolium.
Thayer-Martin Agar, Modified (MTM II) (Modified Thayer-Martin Agar) Composition per liter: Agar ..................................................................12.0g Hemoglobin ......................................................10.0g Pancreatic digest of casein..................................7.5g Selected meat peptone ........................................7.5g NaCl....................................................................5.0g K2HPO4...............................................................4.0g
414
Thayer-Martin Medium
Cornstarch...........................................................1.0g KH2PO4 ...............................................................1.0g CNVT inhibitor............................................. 10.0mL Supplement solution ..................................... 10.0mL pH 7.2 ± 0.2 at 25°C
Hemoglobin solution .................................. 250.0mL Vitox supplement .......................................... 10.0mL pH 7.3 ± 0.2 at 25°C
CNVT Inhibitor: Composition per 10.0mL:
Special peptone.................................................15.0g Agar ..................................................................10.0g NaCl....................................................................5.0g K2HPO4...............................................................4.0g Cornstarch...........................................................1.0g KH2PO4...............................................................1.0g pH 7.2 ± 0.2 at 25°C
Colistin sulfate .................................................7.5mg Trimethoprim lactate........................................5.0mg Vancomycin .....................................................3.0mg Nystatin........................................................12,500U
Preparation of CNVT Inhibitor: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Supplement Solution: Composition per liter: Glucose ...........................................................100.0g L-Cysteine·HCl..................................................25.9g L-Glutamine.......................................................10.0g L-Cystine .............................................................1.1g Adenine...............................................................1.0g Nicotinamide adenine dinucleotide ..................0.25g Vitamin B12 .........................................................0.1g Thiamine pyrophosphate.....................................0.1g Guanine·HCl .....................................................0.03g Fe(NO3)3·6H2O .................................................0.02g p-Aminobenzoic acid......................................0.013g Thiamine·HCl ..................................................3.0mg
Source: The supplement solution IsoVitaleX enrichment is available from BD Diagnostic Systems. This enrichment may be replaced by supplement VX from BD Diagnostic Systems.
Preparation of Supplement Solution: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except CNVT inhibitor and supplement solution, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 10.0mL of sterile CNVT inhibitor and 10.0mL of sterile supplement solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation of Neisseria species from specimens containing mixed flora of bacteria and fungi.
Thayer-Martin Medium
GC Agar Base: Composition per 740.0mL:
Preparation of GC Agar Base: Add components of GC medium base and the hemoglobin to distilled/deionized water and bring volume to 740.0mL. Mix thoroughly. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C.
Hemoglobin Solution: Composition per 250.0mL: Hemoglobin ........................................................5.0g
Preparation of Hemoglobin Solution: Add hemoglobin to distilled/deionized water and bring volume to 250.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Vitox Supplement: Composition per 10.0mL: Glucose ...............................................................2.0g L-Cysteine·HCl ...............................................0.518g L-Glutamine ........................................................0.2g L-Cystine.........................................................0.022g Adenine sulfate .................................................0.01g Nicotinamide adenine dinucleotide .................5.0mg Cocarboxylase..................................................2.0mg Guanine·HCl ....................................................0.6mg Fe(NO3)3·6H2O................................................0.4mg p-Aminobenzoic acid.....................................0.26mg Vitamin B12 ......................................................0.2mg Thiamine·HCl ................................................0.06mg
Preparation of Vitox Supplement: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: To 740.0mL of cooled sterile GC agar base, aseptically add 250.0mL of sterile hemoglobin solution and 10.0mL of sterile Vitox supplement. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes. Use: For the isolation and cultivation of fastidious microorganisms, especially Neisseria species.
Thayer-Martin Medium
Composition per liter:
Composition per liter:
GC agar base............................................... 740.0mL
Hemoglobin ......................................................10.0g
Thayer-Martin Medium, Modified
415
GC medium base......................................... 980.0mL CNVT inhibitor............................................. 10.0mL Supplement B................................................ 10.0mL pH 7.3 ± 0.2 at 25°C
Cornstarch...........................................................1.0g KH2PO4...............................................................1.0g pH 7.2 ± 0.2 at 25°C
Source: This medium is available as a prepared me-
nents of GC medium base and the hemoglobin to distilled/deionized water and bring volume to 720.0mL. Mix thoroughly. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C.
dium in tubes from BD Diagnostic Systems.
GC Medium Base: Composition per 980.0mL: Proteose peptone no. 3 ......................................15.0g Agar ..................................................................10.0g NaCl ....................................................................5.0g K2HPO4 ...............................................................4.0g Cornstarch...........................................................1.0g KH2PO4 ...............................................................1.0g pH 7.2 ± 0.2 at 25°C
Preparation of GC Medium Base: Add components of GC medium base and the hemoglobin to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
CNVT Inhibitor: Composition per 10.0mL: Colistin sulfate .................................................7.5mg Trimethoprim lactate........................................5.0mg Vancomycin .....................................................3.0mg Nystatin........................................................12,500U
Preparation of CNVT Inhibitor: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: To 980.0mL of cooled sterile GC medium base, aseptically add 10.0mL of sterile CNVT inhibitor and 10.0mL of sterile supplement B. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes. Use: For the isolation and cultivation of fastidious microorganisms, especially Neisseria species.
Thayer-Martin Medium, Modified (Modified Thayer-Martin Agar) Composition per liter: GC agar base............................................... 720.0mL Hemoglobin solution................................... 250.0mL GC supplement ............................................. 30.0mL pH 7.3 ± 0.2 at 25°C
GC Agar Base: Composition per 720.0mL: Special peptone .................................................15.0g Agar ..................................................................10.0g NaCl ....................................................................5.0g K2HPO4 ...............................................................4.0g
Preparation of GC Agar Base: Add compo-
Hemoglobin Solution: Composition per 250.0mL: Hemoglobin ........................................................5.0g
Preparation of Hemoglobin Solution: Add hemoglobin to distilled/deionized water and bring volume to 250.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
GC Supplement: Composition per 30.0mL: Yeast autolysate ................................................10.0g Glucose ...............................................................1.5g NaHCO3 ............................................................0.15g Colistin sulfate .................................................7.5mg Trimethoprim lactate........................................5.0mg Vancomycin .....................................................3.0mg Nystatin........................................................ 12,500U
Preparation of GC Supplement: Add components to distilled/deionized water and bring volume to 30.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: To 720.0mL of cooled sterile GC agar base, aseptically add 250.0mL of sterile hemoglobin solution and 30.0mL of sterile GC supplement. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes. Use: For the selective isolation and cultivation of fastidious microorganisms, especially Neisseria species.
Thayer-Martin Medium, Modified (Modified Thayer-Martin Agar) Composition per liter: GC agar base............................................... 730.0mL Hemoglobin solution .................................. 250.0mL Vitox supplement .......................................... 10.0mL VCNT antibiotic solution ............................. 10.0mL pH 7.3 ± 0.2 at 25°C
GC Agar Base: Composition per 730.0mL: Special peptone.................................................15.0g Agar ..................................................................10.0g NaCl....................................................................5.0g K2HPO4...............................................................4.0g Cornstarch...........................................................1.0g KH2PO4...............................................................1.0g pH 7.2 ± 0.2 at 25°C
416
Thayer-Martin Medium, Selective
Preparation of GC Agar Base: Add components of GC medium base and the hemoglobin to distilled/deionized water and bring volume to 730.0mL. Mix thoroughly. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°– 50°C.
Hemoglobin Solution: Composition per 250.0mL: Hemoglobin ........................................................5.0g
Preparation of Hemoglobin Solution: Add hemoglobin to distilled/deionized water and bring volume to 250.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Vitox Supplement: Composition per 10.0mL: Glucose ...............................................................2.0g L-Cysteine·HCl ...............................................0.518g L-Glutamine........................................................0.2g L-Cystine ........................................................0.022g Adenine sulfate .................................................0.01g Nicotinamide adenine dinucleotide .................5.0mg Cocarboxylase..................................................2.0mg Guanine·HCl ....................................................0.6mg Fe(NO3)3·6H2O ................................................0.4mg p-Aminobenzoic acid.....................................0.26mg Vitamin B12 ......................................................0.2mg Thiamine·HCl ................................................0.06mg
Preparation of Vitox Supplement: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
VCNT Antibiotic Solution: Composition per 10.0mL: Colistin methane sulfonate...............................7.5mg Trimethoprim lactate........................................5.0mg Vancomycin .....................................................3.0mg Nystatin.........................................................12500U
Preparation of VCNT Antibiotic Solution: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: To 730.0mL of cooled, sterile GC agar base, aseptically add 250.0mL of sterile hemoglobin solution, 10.0mL of sterile Vitox supplement, and 10.0mL of VCNT antibiotic solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes. Use: For the selective isolation and cultivation of fastidious microorganisms, especially Neisseria species.
Thayer-Martin Medium, Selective Composition per liter: GC agar base............................................... 730.0mL
Hemoglobin solution .................................. 250.0mL Vitox supplement .......................................... 10.0mL VCN antibiotic solution................................ 10.0mL pH 7.3 ± 0.2 at 25°C
GC Agar Base: Composition per 730.0mL: Special peptone.................................................15.0g Agar ..................................................................10.0g NaCl....................................................................5.0g K2HPO4...............................................................4.0g Cornstarch...........................................................1.0g KH2PO4...............................................................1.0g pH 7.2 ± 0.2 at 25°C
Preparation of GC Agar Base: Add components of GC medium base and the hemoglobin to distilled/deionized water and bring volume to 730.0mL. Mix thoroughly. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°– 50°C.
Hemoglobin Solution: Composition per 250.0mL: Hemoglobin ........................................................5.0g
Preparation of Hemoglobin Solution: Add hemoglobin to distilled/deionized water and bring volume to 250.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Vitox Supplement: Composition per 10.0mL: Glucose ...............................................................2.0g L-Cysteine·HCl ...............................................0.518g L-Glutamine ........................................................0.2g L-Cystine.........................................................0.022g Adenine sulfate .................................................0.01g Nicotinamide adenine dinucleotide .................5.0mg Cocarboxylase..................................................2.0mg Guanine·HCl ....................................................0.6mg Fe(NO3)3·6H2O................................................0.4mg p-Aminobenzoic acid.....................................0.26mg Vitamin B12 ......................................................0.2mg Thiamine·HCl ................................................0.06mg
Preparation of Vitox Supplement: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
VCN Antibiotic Solution: Composition per 10.0mL: Colistin methane sulfonate ..............................7.5mg Vancomycin .....................................................3.0mg Nystatin........................................................ 12,500U
Preparation of VCN Antibiotic Solution: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Thioglycolate Bile Broth Preparation of Medium: To 730.0mL of cooled, sterile GC agar base, aseptically add 250.0mL of sterile hemoglobin solution, 10.0mL of sterile Vitox supplement, and 10.0mL of VCN antibiotic solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes. Use: For the selective isolation and cultivation of fastidious microorganisms, especially Neisseria species.
Thayer-Martin Selective Agar Composition per liter: Agar ..................................................................12.0g Hemoglobin ......................................................10.0g Pancreatic digest of casein..................................7.5g Selected meat peptone ........................................7.5g NaCl ....................................................................5.0g K2HPO4 ...............................................................4.0g Cornstarch...........................................................1.0g KH2PO4 ...............................................................1.0g Supplement solution ..................................... 10.0mL VCN inhibitor ............................................... 10.0mL pH 7.2 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Supplement Solution: Composition per liter: Glucose ...........................................................100.0g L-Cysteine·HCl..................................................25.9g L-Glutamine.......................................................10.0g L-Cystine .............................................................1.1g Adenine...............................................................1.0g Nicotinamide adenine dinucleotide ..................0.25g Vitamin B12 .........................................................0.1g Thiamine pyrophosphate.....................................0.1g Guanine·HCl .....................................................0.03g Fe(NO3)3·6H2O .................................................0.02g p-Aminobenzoic acid......................................0.013g Thiamine·HCl ..................................................3.0mg
417
Preparation of VCN Inhibitor: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except supplement solution and VCN inhibitor, to distilled/deionized water and bring volume to 980.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile VCN inhibitor and sterile supplement solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the selective isolation of Neisseria gonorrhoeae and Neisseria meningitidis from specimens containing mixed flora of bacteria and fungi.
Thiogel® Medium Composition per liter: Gelatin...............................................................50.0g Pancreatic digest of casein................................17.0g Glucose ...............................................................6.0g Papaic digest of soybean meal............................3.0g NaCl....................................................................2.5g Agar ....................................................................0.7g Sodium thioglycolate ..........................................0.5g L-Cystine ...........................................................0.25g Na2SO3 ................................................................0.1g pH 7.0 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components to distilled/deionized water preheated to 50°C and bring volume to 1.0L. Mix thoroughly. Let stand for 5 min. Gently heat while stirring and bring to boiling. Distribute into tubes, filling them half full. Autoclave for 15 min at 13 psi pressure–118°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the differentiation of microorganisms based on their ability to liquefy gelatin.
Source: The supplement solution IsoVitaleX enrichment is available from BD Diagnostic Systems. This enrichment may be replaced by supplement VX from BD Diagnostic Systems.
Preparation of Supplement Solution: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
VCN Inhibitor: Composition per 10.0mL: Colistin.............................................................7.5mg Vancomycin .....................................................3.0mg Nystatin........................................................12,500U
Thioglycolate Bile Broth Composition per 1050.0mL: Pancreatic digest of casein................................15.0g Glucose ...............................................................5.5g Yeast extract........................................................5.0g NaCl....................................................................2.5g Agar ..................................................................0.75g L-Cystine .............................................................0.5g Sodium thioglycolate ..........................................0.5g Bile solution.................................................. 50.0mL pH 7.1 ± 0.2 at 25°C
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Thioglycolate Broth USP, Alternative
Bile Solution: Composition per 100.0mL: Oxgall................................................................40.0g Sodium deoxycholate..........................................2.0g
Preparation of Bile Solution: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except bile solution, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes in 10.0mL volumes. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C. Aseptically add 0.5mL of sterile bile solution to each tube. Mix thoroughly.
Use: For the cultivation of Bacteroides fragilis and Clostridium perfringens from clinical specimens.
Thioglycolate Broth USP, Alternative Composition per liter: Pancreatic digest of casein................................15.0g Glucose ...............................................................5.5g Yeast extract........................................................5.0g NaCl ....................................................................2.5g L-Cystine .............................................................0.5g Sodium thioglycolate ..........................................0.5g pH 7.1 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Prepare freshly or boil and cool the medium just before use.
Use: For the cultivation of both aerobic and anaerobic organisms in the performance of sterility tests of turbid or viscous specimens.
Thioglycolate Gelatin Medium Composition per liter: Gelatin...............................................................50.0g Pancreatic digest of casein................................15.0g Yeast extract........................................................5.0g NaCl ....................................................................2.5g Glucose ...............................................................2.0g Agar ..................................................................0.75g L-Cystine ...........................................................0.25g Na2SO3 ................................................................0.1g Thioglycollic acid ........................................... 0.3mL pH 7.0 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to 50°C. Let stand 5 min. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the determination of gelatin liquefaction by aerobes, microaerophiles, and anaerobes without special incubation.
Thioglycolate Medium (DSMZ Medium 530) Composition per liter: Agar ..................................................................15.0g Peptone from casein............................................5.0g Meat extract ........................................................3.0g Na-thioglycolate solution............................ 100.0mL pH 5.5 ± 0.2 at 25°C
Thioglycolate Solution : Composition per 100.0mL: Na-Thioglycolate ................................................0.5g
Preparation of Thioglycolate Solution: Add thioglycolate to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize. Warm to 50°C.
Preparation of Medium: Add components, except thiglycolate solution, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C. Aseptically add 100.0mL warm thioglycolate solution. Adjust pH to 5.5. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation and maintenance of various anaerobic bacteria.
Thioglycolate Medium with 20% Bile (THIO + Bile Medium) Composition per liter: Oxgall ...............................................................20.0g Thioglycolate medium without indicator........... 1.0L Hemin solution................................................ 0.5mL Vitamin K1 solution ........................................ 0.1mL pH 7.0 ± 0.2 at 25°C
Thioglycolate Medium without Indicator: Composition per liter: Pancreatic digest of casein................................17.0g Glucose ...............................................................6.0g Papaic digest of soybean meal............................3.0g NaCl....................................................................2.5g Agar ....................................................................0.7g Sodium thioglycolate ..........................................0.5g
Thioglycolate Medium, Enriched L-Cystine ...........................................................0.25g
Na2SO3 ................................................................0.1g
Preparation of Thioglycolate Medium Without Indicator: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly.
Vitamin K1 Solution: Composition per 100.0mL: Vitamin K1 ..........................................................1.0g
Preparation of Vitamin K1 Solution: Add vitamin K1 to 99.0mL of absolute ethanol. Mix thoroughly.
Hemin Solution: Composition per 100.0mL: Hemin..................................................................1.0g NaOH (1N solution)...................................... 20.0mL
Preparation of Hemin Solution: Add hemin to 20.0mL of 1N NaOH solution. Mix thoroughly. Bring volume to 100.0mL with distilled/deionized water.
Preparation of Medium: Add 0.5mL of hemin solution, 0.1mL of vitamin K1 solution, and oxgall to 1.0L of thioglycolate medium without indicator. Mix thoroughly. Distribute into screw-capped tubes or flasks. Autoclave for 15 min at 15 psi pressure– 121°C. Cool tubes or flasks under 85% N2 + 10% H2 + 5% CO2. Tighten caps.
Use: For the isolation, cultivation, and identification of a variety of obligate anaerobic bile-tolerant bacteria.
Thioglycolate Medium, Brewer Composition per liter: Glucose ...............................................................5.0g Peptone................................................................5.0g NaCl ....................................................................5.0g Yeast extract........................................................2.0g Sodium thioglycolate ..........................................1.1g Agar ....................................................................1.0g Beef extract .........................................................1.0g Methylene Blue................................................2.0mg pH 7.2 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
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Thioglycolate Medium, Brewer Modified Composition per liter: Pancreatic digest of casein................................17.5g Glucose .............................................................10.0g NaCl....................................................................5.0g Papaic digest of soybean meal............................2.5g K2HPO4...............................................................2.0g Sodium thioglycolate ..........................................1.0g Agar ....................................................................0.5g Methylene Blue...............................................0.002g pH 7.2 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Distribute into tubes or flasks, filling them half full. Autoclave for 15 min at 15 psi pressure– 121°C.
Use: For the cultivation of obligate anaerobes, microaerophiles, and facultative organisms.
Thioglycolate Medium, Enriched (THIO Medium) (Thioglycolate Medium with Vitamin K1 and Hemin)
Composition per liter:
Thioglycolate medium without indicator........... 1.0L Hemin solution................................................ 0.5mL Vitamin K1 solution ........................................ 0.1mL pH 7.0 ± 0.2 at 25°C
Thioglycolate Medium without Indicator: Composition per liter: Pancreatic digest of casein................................17.0g Glucose ...............................................................6.0g Papaic digest of soybean meal............................3.0g NaCl....................................................................2.5g Agar ....................................................................0.7g Sodium thioglycolate ..........................................0.5g L-Cystine ...........................................................0.25g Na2SO3 ................................................................0.1g
Source: Thioglycolate medium without indicator is available as a premixed powder from Oxoid Unipath and BD Diagnostic Systems.
Preparation of Thioglycolate Medium without Indicator: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly.
Use: For determination of the sterility of solutions
Vitamin K1 Solution: Composition per 100.0mL:
containing mercurial preservatives.
Vitamin K1 ..........................................................1.0g
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Thioglycolate Medium without Glucose
Preparation of Vitamin K1 Solution: Add vita-
L-Cystine ...........................................................0.25g
min K1 to 99.0mL of absolute ethanol. Mix thoroughly.
Thioglycollic acid ........................................... 0.3mL pH 7.2 ± 0.2 at 25°C
Hemin Solution: Composition per 100.0mL:
Source: This medium is available as a premixed
Hemin..................................................................1.0g NaOH (1N solution)...................................... 20.0mL
Preparation of Medium: Add components to
Preparation of Hemin Solution: Add hemin to 20.0mL of 1N NaOH solution. Mix thoroughly. Bring volume to 100.0mL with distilled/deionized water.
Preparation of Medium: Add 0.5mL of hemin
powder from BD Diagnostic Systems. distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. If medium becomes oxidized before use, heat in a boiling water bath to expel absorbed O2. Cool to 25°C.
solution and 0.1mL of vitamin K1 solution to 1.0L of thioglycolate medium without indicator. Mix thoroughly. Distribute into screw-capped tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Cool tubes or flasks under 85% N2 + 10% H2 + 5% CO2. Tighten caps.
Use: For the cultivation of anaerobic, microaero-
Use: For the isolation, cultivation, and identification
Composition per liter:
of a wide variety of obligate anaerobic bacteria.
Thioglycolate Medium without Glucose Composition per liter: Pancreatic digest of casein................................15.0g Yeast extract........................................................5.0g NaCl ....................................................................2.5g Agar ..................................................................0.75g L-Cystine ...........................................................0.25g Methylene Blue................................................2.0mg Thioglycollic acid ........................................... 0.3mL pH 7.2 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. If medium becomes oxidized before use (Methylene Blue turns blue), heat in a boiling water bath to expel absorbed O2. Cool to 25°C.
Use: For the cultivation of anaerobic, microaerophilic, and aerobic microorganisms. For use in sterility testing of a variety of specimens.
Thioglycolate Medium without Glucose and Indicator Composition per liter: Pancreatic digest of casein................................15.0g Yeast extract........................................................5.0g NaCl ....................................................................2.5g Agar ..................................................................0.75g
philic, and aerobic microorganisms. For use in sterility testing of a variety of specimens.
Thioglycolate Medium without Indicator Pancreatic digest of casein................................15.0g Yeast extract........................................................5.0g Glucose ...............................................................5.0g NaCl....................................................................2.5g Agar ..................................................................0.75g Sodium thioglycolate ..........................................0.5g L-Cystine ...........................................................0.25g pH 7.2 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. If medium becomes oxidized before use, heat in a boiling water bath to expel absorbed O2. Cool to 25°C.
Use: For the cultivation of anaerobic, microaerophilic, and aerobic microorganisms. For use in sterility testing of a variety of specimens.
Thioglycolate Medium without Indicator Composition per liter: Pancreatic digest of casein................................17.0g Glucose ...............................................................6.0g Papaic digest of soybean meal............................3.0g NaCl....................................................................2.5g Agar ....................................................................0.7g Sodium thioglycolate ..........................................0.5g L-Cystine ...........................................................0.25g Na2SO3 ................................................................0.1g pH 7.0 ± 0.2 at 25°C
Thioglycolate Medium, USP Source: This medium is available as a premixed powder from Oxoid Unipath. Preparation of Medium: Add components to
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Na2CO3 solution........................................... 10.0mL Vitamin K1 solution ...................................... 10.0mL pH 7.2 ± 0.2 at 25°C
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Prepare freshly or boil and cool the medium just before use.
Na2CO3 Solution: Composition per 10.0mL:
Use: For the growth of aerobic and anaerobic micro-
Preparation of Na2CO3 Solution: Add Na2CO3
organisms in diagnostic bacteriology.
Thioglycolate Medium without Indicator-135C Composition per liter: Pancreatic digest of casein................................17.0g Glucose ...............................................................6.0g Papaic digest of soybean meal ............................3.0g NaCl ....................................................................2.5g Agar ....................................................................0.7g Sodium thioglycolate ..........................................0.5g Na2SO3 ................................................................0.1g L-Cystine ...........................................................0.25g pH 7.0 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Distribute into tubes or flasks, filling them half full. For maintenance of cultures, a small quantity of CaCO3 may be added to tubes before adding medium. Autoclave for 15 min at 13 psi pressure– 118°C. Prepare freshly or boil and cool the medium just before use. Store prepared medium at 2°–8°C in the dark.
Use: For the isolation and cultivation of a wide variety of microorganisms, particularly obligate anaerobes, from clinical specimens and other materials.
Thioglycolate Medium without Indicator with Hemin (Thioglycolate Medium, Supplemented) Composition per liter: Pancreatic digest of casein................................17.0g CaCO3, chips or powder ...................................10.0g Glucose ...............................................................6.0g Papaic digest of soybean meal ............................3.0g NaCl ....................................................................2.5g Agar ....................................................................0.7g Sodium thioglycolate ..........................................0.5g L-Cystine ...........................................................0.25g Na2SO3 ................................................................0.1g Hemin...............................................................5.0mg
Na2CO3 ...............................................................1.0g to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Vitamin K1 Solution: Composition per 100.0mL: Vitamin K1 ..........................................................1.0g Ethanol, absolute........................................... 99.0mL
Preparation of Vitamin K1 Solution: Add vitamin K1 to 99.0mL of absolute ethanol. Mix thoroughly.
Preparation of Medium: Add components, except CaCO3, Na2CO3 solution, and vitamin K1 solution, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Add 0.1g of CaCO3 chips or powder to each of 100 test tubes. Distribute broth into the same tubes in 10.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 0.1mL of sterile Na2CO3 solution and 0.1mL of sterile vitamin K1 solution to each tube. Mix thoroughly.
Use: For the cultivation of a wide variety of obligate anaerobes.
Thioglycolate Medium, USP Composition per liter: Pancreatic digest of casein................................15.0g Glucose ...............................................................5.5g Yeast extract........................................................5.0g NaCl....................................................................2.5g Agar ....................................................................0.5g L-Cystine .............................................................0.5g Sodium thioglycolate ..........................................0.5g Resazurin .........................................................1.0mg pH 7.1 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of both aerobic and anaerobic organisms in the performance of sterility tests.
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Thiol Medium
Thiol Medium Composition per liter: Proteose peptone no. 3 ......................................10.0g Thiol complex .....................................................8.0g Yeast extract........................................................5.0g NaCl ....................................................................5.0g Glucose ...............................................................1.0g Agar ....................................................................1.0g p-Aminobenzoic acid........................................0.05g pH 7.1 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. For neutralization of penicillin, distribute medium into tubes to a depth of 60 mm. For neutralization of streptomycin, distribute medium into tubes in shallow layers. Autoclave for 15 min at 15 psi pressure–121°C.
thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the primary isolation and identification of Corynebacterium diphtheriae.
Tissue Culture Amino Acids, HeLa 100X (TC Amino Acids, HeLa 100X) Composition per liter: L-Lysine...........................................................0.029g L-Isoleucine .....................................................0.026g L-Leucine
........................................................0.026g
L-Threonine .....................................................0.023g L-Valine ...........................................................0.023g L-Tyrosine
.......................................................0.018g
L-Arginine .......................................................0.017g L-Phenylalanine...............................................0.016g L-Cystine .........................................................0.012g L-Histidine........................................................7.8mg L-Methionine ....................................................7.5mg L-Tryptophan....................................................4.1mg
Use: For the cultivation of bacteria from body fluids
pH 7.2–7.4 at 25°C
and other materials containing penicillin, streptomycin, or sulfonamides. Also used for the cultivation and maintenance of Bifidobacterium species.
Preparation of Tissue Culture Amino Acids, HeLa 100X: Add components to distilled/deion-
Tinsdale Agar
Use: For the preparation of Eagle HeLa medium for
Composition per 1100.0mL: Proteose peptone ...............................................20.0g Agar ..................................................................15.0g NaCl ....................................................................5.0g Yeast extract........................................................5.0g L-Cystine ...........................................................0.24g Tinsdale supplement ................................... 150.0mL pH 7.4 ± 0.2 at 25°C
ized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.2–7.4. Filter sterilize. tissue culture procedures and virual culture.
Tissue Culture Amino Acids, Minimal Eagle 50X (TC Amino Acids, Minimal Eagle 50X) Composition per liter:
Source: This medium is available as a premixed
L-Arginine ...........................................................0.1g
powder from BD Diagnostic Systems and Oxoid Unipath.
L-Isoleucine .....................................................0.052g
Tinsdale Supplement: Composition per 100.0mL: Na2S2O3 ............................................................0.43g K2TeO3 ..............................................................0.35g Serum .......................................................... 100.0mL
Caution: Potassium tellurite is toxic. Preparation of Tinsdale Supplement: Add Na2S2O3 and K2TeO3 to serum. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except Tinsdale supplement, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Aseptically add 100.0mL of sterile Tinsdale supplement. Mix
L-Lysine...........................................................0.058g L-Leucine
........................................................0.052g
L-Threonine .....................................................0.048g L-Valine ...........................................................0.046g L-Tyrosine
.......................................................0.036g
L-Phenylalanine...............................................0.032g L-Histidine.......................................................0.031g L-Cystine .........................................................0.024g L-Methionine ...................................................0.015g L-Tryptophan.....................................................0.01g
pH 7.2–7.4 at 25°C
Preparation of Tissue Culture Amino Acids, Minimal Eagle 50X: Add components to distilled/ deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.2–7.4. Filter sterilize.
Use: For the preparation of TC minimal medium Eagle for tissue culture procedures and virus studies.
Tissue Culture Medium 199
Tissue Culture Dulbecco Solution (TC Dulbecco Solution) Composition per liter: NaCl ....................................................................8.0g Na2HPO4 ...........................................................1.15g KH2PO4 ...............................................................0.2g KCl......................................................................0.2g CaCl2·2H2O.........................................................0.1g MgCl2·6H2O .......................................................0.1g pH 7.2–7.4 at 25°C
Preparation of Tissue Culture Dulbecco Solution: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.2–7.4. Filter sterilize.
Use: For use in tissue culture and virus preparations.
Tissue Culture Earle Solution (TC Earle Solution) Composition per 1002.0mL: NaCl ....................................................................6.8g NaHCO3 ..............................................................2.2g Glucose ...............................................................1.0g KCl......................................................................0.4g CaCl2·2H2O.........................................................0.2g NaH2PO4 .........................................................0.125g MgSO4·7H2O ......................................................0.1g Phenol Red (1% solution) ............................... 2.0mL pH 7.2–7.4 at 25°C
Preparation of Tissue Culture Earle Solution: Add components, except Phenol Red, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Add 2.0mL of Phenol Red solution. Adjust pH to 7.2–7.4. Filter sterilize.
Use: For use in tissue culture and virus preparations.
Tissue Culture Hanks Solution (TC Hanks Solution) Composition per liter: NaCl ....................................................................8.0g Glucose ...............................................................1.0g KCl......................................................................0.4g NaHCO3 ............................................................0.35g CaCl2·2H2O.......................................................0.14g MgCl2·6H2O .......................................................0.1g MgSO4·7H2O ......................................................0.1g Na2HPO4 ...........................................................0.06g KH2PO4 .............................................................0.06g Phenol Red........................................................0.02g pH 7.2–7.4 at 25°C
Source: This medium is available as a premixed solution from BD Diagnostic Systems.
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Preparation of Tissue Culture Hanks Solution: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.2–7.4. Filter sterilize.
Use: For use in tissue culture procedures.
Tissue Culture Medium 199 (TC Medium 199) Composition per 1050.0mL: NaCl....................................................................8.0g Glucose ...............................................................1.0g KCl......................................................................0.4g NaHCO3 ............................................................0.35g DL-Glutamic acid...............................................0.15g CaCl2·2H2O ......................................................0.14g DL-Leucine ........................................................0.12g L-Glutamine ........................................................0.1g MgSO4·7H2O ......................................................0.1g L-Arginine .........................................................0.07g L-Lysine.............................................................0.07g DL-Aspartic acid ................................................0.06g Na2HPO4 ...........................................................0.06g KH2PO4.............................................................0.06g DL-Threonine.....................................................0.06g DL-Alanine ........................................................0.05g Glycine..............................................................0.05g DL-Phenylalanine ..............................................0.05g DL-Serine ...........................................................0.05g Sodium acetate..................................................0.05g DL-Valine ...........................................................0.05g DL-Isoleucine.....................................................0.04g L-Proline............................................................0.04g L-Tyrosine .........................................................0.04g DL-Methionine...................................................0.03g L-Cystine ...........................................................0.02g L-Histidine.........................................................0.02g Phenol Red........................................................0.02g DL-Tryptophan...................................................0.02g Adenine.............................................................0.01g L-Hydroxyproline..............................................0.01g Tween 80..........................................................5.0mg Adenosine triphosphate ...................................1.0mg Choline.............................................................0.5mg Deoxyribose.....................................................0.5mg Ribose ..............................................................0.5mg Guanine............................................................0.3mg Hypoxanthine...................................................0.3mg Thymine...........................................................0.3mg Uracil ...............................................................0.3mg Xanthine...........................................................0.3mg Adenylic acid ...................................................0.2mg Cholesterol.......................................................0.2mg Calciferol .........................................................0.1mg Fe(NO3)3·9H2O................................................0.1mg
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Tissue Culture Medium Eagle with Earle Balanced Salt Solution
L-Cysteine
........................................................0.1mg Vitamin A.........................................................0.1mg p-Aminobenzoic acid.....................................0.05mg Ascorbic acid .................................................0.05mg Glutathione.....................................................0.05mg Inositol ...........................................................0.05mg Niacin...........................................................0.025mg Niacinamide .................................................0.025mg Pyridoxine·HCl ............................................0.025mg Pyridoxal·HCl ..............................................0.025mg α-Tocopherol phosphate ................................0.01mg Biotin .............................................................0.01mg Calcium pantothenate ....................................0.01mg Folic acid........................................................0.01mg Menadione .....................................................0.01mg Riboflavin ......................................................0.01mg Thiamine·HCl ................................................0.01mg Serum ................................................. 50.0–100.0mL pH 7.2–7.4 at 25°C
L-Cystine .........................................................0.012g
Preparation of Medium: Add components, ex-
L-Glutamine
cept serum, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.2– 7.4 with 10% Na2CO3 solution. Filter sterilize. Aseptically add 50.0–100.0mL of sterile serum. Human serum, bovine serum, horse serum, or fetal calf serum may be used. Mix thoroughly. If desired, antibacterial inhibitors may be added. Aseptically add 500,000U of penicillin and 0.5g of streptomycin to 1050.0mL of the complete medium to increase selectivity.
Use: For the cultivation of a wide variety of cell lines in tissue culture. It is especially useful for the detection, titering, and identification of viruses in tissue culture cells.
Tissue Culture Medium Eagle with Earle Balanced Salt Solution (TC Medium Eagle with Earle BSS)
L-Histidine........................................................8.0mg L-Methionine ....................................................7.5mg
Phenol Red.......................................................5.0mg L-Tryptophan....................................................4.0mg Inositol .............................................................1.8mg Biotin ...............................................................1.0mg Calcium pantothenate ......................................1.0mg Choline chloride...............................................1.0mg Folic acid .........................................................1.0mg Nicotinamide....................................................1.0mg Pyridoxal·HCl ..................................................1.0mg Thiamine·HCl ..................................................1.0mg Riboflavin ........................................................0.1mg Serum................................................. 50.0–100.0mL Glutamine solution.......................................... 6.0mL pH 7.2–7.4 at 25°C
Glutamine Solution: Composition per 100.0mL: ........................................................5.0g NaCl (0.85% solution) ................................ 100.0mL
Preparation of Glutamine Solution: Add the glutamine to the 0.85% NaCl solution. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except glutamine and serum, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.2–7.4. Filter sterilize. Aseptically add 6.0mL of sterile glutamine solution and 50.0–100.0mL of sterile serum. Human serum, bovine serum, horse serum, or fetal calf serum may be used. Mix thoroughly.
Use: For the cultivation of HeLa, KB, and other tissue culture cell lines.
Tissue Culture Medium Eagle with Hanks Balanced Salt Solution (TC Medium Eagle with Hanks BSS)
Composition per 1056.0mL:
Composition per 1056.0mL:
NaCl ....................................................................6.8g NaHCO3 ..............................................................2.2g Glucose ...............................................................1.0g KCl......................................................................0.4g CaCl2·2H2O.........................................................0.2g NaH2PO4 .........................................................0.125g MgSO4·7H2O ......................................................0.1g L-Isoleucine .....................................................0.026g L-Leucine.........................................................0.026g L-Lysine...........................................................0.026g L-Threonine .....................................................0.024g L-Valine .........................................................0.0235g L-Tyrosine........................................................0.018g L-Arginine .....................................................0.0174g L-Phenylalanine.............................................0.0165g
NaCl....................................................................8.0g Glucose ...............................................................1.0g KCl......................................................................0.4g CaCl2·2H2O ......................................................0.14g MgSO4·7H2O ......................................................0.1g KH2PO4.............................................................0.06g Na2HPO4 ...........................................................0.05g L-Isoleucine .....................................................0.026g L-Leucine ........................................................0.026g L-Lysine...........................................................0.026g L-Threonine .....................................................0.024g L-Valine .........................................................0.0235g L-Tyrosine .......................................................0.018g L-Arginine .....................................................0.0174g L-Phenylalanine.............................................0.0165g
Tissue Culture Medium Ham F10
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L-Cystine .........................................................0.012g
L-Cystine .........................................................0.012g
L-Histidine........................................................8.0mg
L-Histidine........................................................7.8mg
L-Methionine ....................................................7.5mg
L-Methionine ....................................................7.5mg
Phenol Red.......................................................5.0mg L-Tryptophan ....................................................4.0mg Inositol .............................................................1.8mg Biotin ...............................................................1.0mg Folic acid..........................................................1.0mg Calcium pantothenate ......................................1.0mg Choline chloride...............................................1.0mg Nicotinamide....................................................1.0mg Pyridoxal·HCl ..................................................1.0mg Thiamine·HCl ..................................................1.0mg Riboflavin ........................................................0.1mg Serum ................................................. 50.0–100.0mL Glutamine solution.......................................... 6.0mL pH 7.2–7.4 at 25°C
Phenol Red.......................................................5.0mg L-Tryptophan....................................................4.1mg Folic acid .......................................................0.44mg Thiamine·HCl ................................................0.34mg Biotin .............................................................0.24mg Pantothenic acid.............................................0.22mg Pyridoxal·HCl ..................................................0.2mg Choline chloride.............................................0.14mg Nicotinamide..................................................0.12mg Riboflavin ......................................................0.04mg Serum............................................50.0mL–100.0mL Glutamine solution.......................................... 6.0mL pH 7.2–7.4 at 25°C
Glutamine Solution: Composition per 100.0mL: L-Glutamine.........................................................5.0g
Glutamine Solution: Composition per 100.0mL: L-Glutamine
........................................................5.0g NaCl (0.85% solution) ................................ 100.0mL
NaCl (0.85% solution) ................................ 100.0mL
Preparation of Glutamine Solution: Add the
Preparation of Glutamine Solution: Add the
glutamine to the 0.85% NaCl solution. Mix thoroughly. Filter sterilize.
glutamine to the 0.85% NaCl solution. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except glutamine and serum, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.2–7.4. Filter sterilize. Aseptically add 6.0mL of sterile glutamine solution and 50.0–100.0mL of sterile serum. Human serum, bovine serum, horse serum, or fetal calf serum may be used. Mix thoroughly.
Use: For use as a base in the preparation of liquid media used for the cultivation of tissue culture cell lines.
Tissue Culture Medium Eagle, HeLa (TC Medium Eagle, HeLa) Composition per 1056.0mL: NaCl ..................................................................5.85g NaHCO3 ............................................................1.68g Glucose ...............................................................0.9g KCl..................................................................0.373g NaH2PO4 .........................................................0.138g MgCl2·6H2O .....................................................0.12g CaCl2·2H2O.......................................................0.11g L-Lysine.........................................................0.0269g L-Isoleucine ...................................................0.0262g L-Leucine.......................................................0.0262g L-Threonine ...................................................0.0238g L-Valine .........................................................0.0234g L-Tyrosine......................................................0.0181g L-Arginine .....................................................0.0174g L-Phenylalanine.............................................0.0165g
Preparation of Medium: Add components, except glutamine and serum, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.2–7.4. Filter sterilize. Aseptically add 6.0mL of sterile glutamine solution and 50.0–100.0mL of sterile serum. Human serum, bovine serum, horse serum, or fetal calf serum may be used. Mix thoroughly.
Use: For the cultivation and maintenance of HeLa and other cell lines in tissue culture, and for studying the cytopathogenicity of viral agents.
Tissue Culture Medium Ham F10 (TC Medium Ham F10) Composition per 1050.0mL: NaCl....................................................................7.4g Glucose ...............................................................1.1g Na2HPO4 ...........................................................0.29g KCl..................................................................0.285g L-Arginine ....................................................... 0.211g MgSO4·7H2O ..................................................0.153g L-Glutamine ..................................................0.1462g Sodium pyruvate............................................... 0.11g KH2PO4...........................................................0.083g CaCl2·2H2O ....................................................0.044g L-Cystine .......................................................0.0315g L-Lysine.........................................................0.0293g L-Histidine.......................................................0.021g L-Asparagine ...................................................0.015g L-Glutamic acid.............................................0.0147g L-Aspartic acid ..............................................0.0133g
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Tissue Culture Medium NCTC 109
L-Leucine.......................................................0.0131g
L-Alanine...........................................................0.03g
L-Proline ........................................................0.0115g
L-Lysine.............................................................0.03g
L-Serine .........................................................0.0105g
L-Arginine .......................................................0.026g
L-Alanine........................................................8.91mg
L-Valine ...........................................................0.025g
Glycine...........................................................7.51mg L-Phenylalanine..............................................4.96mg L-Methionine ..................................................4.48mg Hypoxanthine...................................................4.0mg L-Threonine ....................................................3.57mg L-Valine ............................................................3.5mg L-Isoleucine ......................................................2.6mg L-Tyrosine.......................................................1.81mg Cyanocobalamin ..............................................1.3mg Folic acid..........................................................1.3mg Phenol Red.......................................................1.2mg Thiamine·HCl ..................................................1.0mg FeSO4·7H2O...................................................0.83mg Calcium pantothenate ......................................0.7mg Thymidine........................................................0.7mg Choline chloride.............................................0.69mg Niacinamide .....................................................0.6mg L-Tryptophan ....................................................0.6mg i-Inositol.........................................................0.54mg Riboflavin ......................................................0.37mg Lipoic acid .......................................................0.2mg Pyridoxine·HCl ................................................0.2mg ZnSO4·7H2O ................................................0.028mg Biotin ...........................................................0.024mg CuSO4·5H2O .................................................... 2.5µg Fetal calf serum.................................. 50.0–100.0mL pH 7.2–7.4 at 25°C
L-Leucine
Preparation of Medium: Add components, except fetal calf serum, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.2–7.4 with 10% Na2CO3 solution. Filter sterilize. Aseptically add 50.0–100.0mL of sterile fetal calf serum. Mix thoroughly.
Use: For the cultivation of a wide variety of cell lines in tissue culture.
Tissue Culture Medium NCTC 109 (TC Medium NCTC 109) Composition per 1050.0mL: NaCl ....................................................................6.8g NaHCO3 ..............................................................2.2g Glucose ...............................................................1.0g KCl......................................................................0.4g L-Cysteine .........................................................0.26g CaCl2·2H2O.........................................................0.2g NaH2PO4 ...........................................................0.14g L-Glutamine.......................................................0.14g MgSO4·7H2O ......................................................0.1g Sodium acetate..................................................0.05g Ascorbic acid ....................................................0.05g
..........................................................0.02g Phenol Red........................................................0.02g L-Histidine.......................................................0.019g L-Threonine .....................................................0.019g L-Isoleucine .....................................................0.018g L-Tryptophan...................................................0.017g L-Phenylalanine...............................................0.017g L-Tyrosine .......................................................0.016g Glycine............................................................0.014g Tween 80.........................................................0.012g L-Serine ........................................................... 0.011g L-Cystine ...........................................................0.01g Glutathione .......................................................0.01g Cyanocobalamin ...............................................0.01g Deoxycytidine...................................................0.01g Deoxyguanosine ...............................................0.01g Deoxyadenosine................................................0.01g Thymidine.........................................................0.01g L-Aspartic acid ...............................................9.91mg L-Glutamic acid..............................................8.26mg L-Arginine ......................................................8.09mg L-Ornithine .....................................................7.38mg Nicotinamide adenine dinucleotide .................7.0mg L-Proline.........................................................6.13mg L-α-N-Butyric acid.........................................5.51mg L-Methionine ..................................................4.44mg L-Taurine ........................................................4.18mg L-Hydroxyproline...........................................4.09mg D-Glucosamine .................................................3.2mg Coenzyme A ....................................................2.5mg Glucuronolactone.............................................1.8mg Sodium glucuronate .........................................1.8mg Choline chloride.............................................1.25mg Cocarboxylase..................................................1.0mg Flavin adenine dinucleotide.............................1.0mg Uridine triphosphate ........................................1.0mg Nicotinamide adenine dinucleotide phosphate..............................1.0mg Vitamin A.......................................................0.25mg Calciferol .......................................................0.25mg i-Inositol.......................................................0.125mg p-Aminobenzoic acid...................................0.125mg 5-Methylcytosine .............................................0.1mg Pyridoxine·HCl ..........................................0.0625mg Pyridoxal·HCl ............................................0.0625mg Niacin.........................................................0.0625mg Niacinamide...............................................0.0625mg Biotin ...........................................................0.025mg Folic acid .....................................................0.025mg Menadione ...................................................0.025mg Pantothenate.................................................0.025mg
Tissue Culture Minimal Medium Eagle Riboflavin ....................................................0.025mg Thiamine·HCl ..............................................0.025mg α-Tocopherol phosphate ..............................0.025mg Serum ................................................. 50.0–100.0mL pH 7.2–7.4 at 25°C
Preparation of Medium: Add components, except serum, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.2– 7.4 with 10% Na2CO3 solution. Filter sterilize. Aseptically add 50.0–100.0mL of sterile serum. Human serum, bovine serum, horse serum, or fetal calf serum may be used. Mix thoroughly.
Use: For the cultivation of a wide variety of cell lines in tissue culture.
Tissue Culture Medium RPMI #1640 (TC Medium RPMI #1640)
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Thiamine·HCl ..................................................1.0mg Calcium pantothenate ....................................0.25mg Biotin ...............................................................0.2mg Riboflavin ........................................................0.2mg Serum................................................. 50.0–100.0mL pH 7.2–7.4 at 25°C
Source: This medium is available as a premixed powder and solution from BD Diagnostic Systems.
Preparation of Medium: Add components, except serum, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.2– 7.4 with 10% Na2CO3 solution. Filter sterilize. Aseptically add 50.0–100.0mL of sterile serum. Human serum, bovine serum, horse serum, or fetal calf serum may be used. Mix thoroughly.
Use: For the cultivation of a wide variety of cell lines in tissue culture.
Composition per liter: NaCl ..................................................................6.46g Glucose ...............................................................2.0g NaHCO3 ..............................................................2.0g NaH2PO4 .........................................................1.512g KCl......................................................................0.4g L-Glutamine.........................................................0.3g L-Arginine ...........................................................0.2g Calcium nitrate....................................................0.1g MgSO4·7H2O ......................................................0.1g L-Asparagine .....................................................0.05g L-Cystine ...........................................................0.05g L-Isoleucine .......................................................0.05g L-Leucine...........................................................0.05g L-Lysine·HCl .....................................................0.04g Inositol ............................................................0.035g L-Serine .............................................................0.03g Hydroxy-L-Proline ............................................0.02g L-Aspartic acid ..................................................0.02g L-Glutamic acid .................................................0.02g L-Proline ............................................................0.02g L-Threonine .......................................................0.02g L-Tyrosine..........................................................0.02g L-Valine .............................................................0.02g L-Histidine.......................................................0.015g L-Methionine ...................................................0.015g L-Phenylalanine...............................................0.015g Glycine..............................................................0.01g L-Tryptophan ....................................................5.0mg Phenol Red...................................................... 5.0mg Vitamin B12 ......................................................5.0mg Choline chloride...............................................3.0mg p-Aminobenzoic acid.......................................1.0mg Folic acid..........................................................1.0mg Glutathione.......................................................1.0mg Nicotinamide....................................................1.0mg Pyridoxine·HCl ................................................1.0mg
Tissue Culture Minimal Medium Eagle Composition per liter: Sterile salt solution ..................................... 944.0mL TC amino acids, minimal Eagle 50X............ 20.0mL TC NaHCO3, 10% ........................................ 20.0mL TC vitamins, minimal Eagle 100X ............... 10.0mL TC glutamine, 5%........................................... 6.0mL pH 7.2–7.4 at 25°C
Sterile Salt Solution: Composition per 944.0mL: NaCl....................................................................6.8g Glucose ...............................................................1.0g KCl......................................................................0.4g CaCl2 ...................................................................0.2g MgCl2..................................................................0.2g NaH2PO4 ...........................................................0.15g
Preparation of Sterile Salt Solution: Add components to distilled/deionized water and bring volume to 944.0mL. Mix thoroughly. Filter sterilize.
Tissue Culture Amino Acids, Minimal Eagle 50X: Composition per liter: L-Arginine ...........................................................0.1g L-Lysine.............................................................0.06g L-Isoleucine .......................................................0.05g L-Leucine
..........................................................0.05g
L-Threonine .......................................................0.05g L-Valine .............................................................0.05g L-Tyrosine
.........................................................0.04g
L-Phenylalanine.................................................0.03g L-Histidine.........................................................0.03g L-Cystine ...........................................................0.02g
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Tissue Culture Minimal Medium Eagle with Earle Balanced Salts Solution
L-Methionine .....................................................0.02g L-Tryptophan .....................................................0.01g
Preparation of Tissue Culture Amino Acids, Minimal Eagle 50X: Add components to distilled/ deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.2–7.4. Filter sterilize.
TC NaHCO3, 10%: Composition per 100.0mL: NaHCO3 ............................................................10.0g
Preparation of TC NaHCO3, 10%: Add NaHCO3 to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
TC Vitamins, Minimal Eagle 100X: Composition per liter: Inositol .............................................................2.0mg Calcium pantothenate ......................................1.0mg Choline chloride...............................................1.0mg Folic acid..........................................................1.0mg Nicotinamide....................................................1.0mg Pyridoxal..........................................................1.0mg Thiamine·HCl ..................................................1.0mg Riboflavin ........................................................0.1mg
Preparation of TC Vitamins, Minimal Eagle 100X: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
TC Glutamine, 5%: Composition per 100.0mL: L-Glutamine.........................................................5.0g
NaCl (0.85% solution) ................................ 100.0mL
Preparation of TC Glutamine, 5%: Add the glutamine to the 0.85% NaCl solution. Mix thoroughly. Filter sterilize. Preparation of Medium: Aseptically combine 944.0mL of sterile salt solution, 20.0mL of sterile TC amino acids, minimal Eagle 50X, 20.0mL of sterile TC NaHCO3, 10%, 10.0mL of sterile TC vitamins, minimal Eagle 100X, and 6.0mL of sterile TC glutamine, 5%. Mix thoroughly. Adjust pH to 7.2– 7.4, if necessary.
Use: For the cultivation of mammalian cells in monolayer or suspension for tissue culture procedures and virus preparation.
Tissue Culture Minimal Medium Eagle with Earle Balanced Salts Solution (TC Minimal Medium Eagle with Earle BSS)
KCl......................................................................0.4g CaCl2·2H2O ........................................................0.2g MgCl2·6H2O .......................................................0.2g NaH2PO4 ...........................................................0.15g L-Arginine ...........................................................0.1g L-Lysine.............................................................0.06g L-Isoleucine .......................................................0.05g L-Leucine ..........................................................0.05g L-Threonine .......................................................0.05g L-Valine .............................................................0.05g L-Tyrosine .........................................................0.04g L-Phenylalanine.................................................0.03g L-Histidine.........................................................0.03g L-Cystine ...........................................................0.02g L-Methionine .....................................................0.02g L-Tryptophan.....................................................0.01g i-Inositol...........................................................2.0mg Calcium pantothenate ......................................1.0mg Choline chloride...............................................1.0mg Folic acid .........................................................1.0mg Nicotinamide....................................................1.0mg Pyridoxal..........................................................1.0mg Thiamine·HCl ..................................................1.0mg Riboflavin ........................................................0.1mg Serum................................................. 50.0–100.0mL Glutamine solution.......................................... 6.0mL CaCl2·2H2O solution (optional)...................... 2.0mL pH 7.2–7.4 at 25°C
Glutamine Solution: Composition per 100.0mL: L-Glutamine
........................................................5.0g NaCl (0.85% solution) ................................ 100.0mL
Preparation of Glutamine Solution: Add the glutamine to the 0.85% NaCl solution. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except glutamine and serum, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.2–7.4 with 10% Na2CO3 solution. Filter sterilize. Aseptically add 6.0mL of sterile glutamine solution and 50.0–100.0mL of sterile serum. Human serum, bovine serum, horse serum, or fetal calf serum may be used. Mix thoroughly. To grow cells in a monolayer, aseptically add 2.0mL of a sterile 10% CaCl2·2H2O solution. To grow cells in suspension, omit the CaCl2·2H2O solution.
Composition per 1056.0mL:
Use: For preparation of Eagle’s minimal medium for
NaCl ....................................................................6.8g Glucose ...............................................................1.0g
the cultivation of cells in monolayer or suspension in tissue culture.
T1N0 Broth
Tissue Culture Minimal Medium Eagle Spinner Modified (TC Minimal Medium Eagle Spinner Modified MEM-S) Composition per 1056.0mL: NaCl ....................................................................6.8g NaHCO3 ..............................................................2.2g NaH2PO4 ...........................................................1.35g Glucose ...............................................................1.0g KCl......................................................................0.4g CaCl2·2H2O.........................................................0.2g NaH2PO4 .........................................................0.125g MgSO4·7H2O ......................................................0.1g L-Isoleucine .....................................................0.026g L-Leucine.........................................................0.026g L-Lysine...........................................................0.026g L-Threonine .....................................................0.024g L-Valine .........................................................0.0235g L-Tyrosine........................................................0.018g L-Arginine .....................................................0.0174g L-Phenylalanine.............................................0.0165g L-Cystine .........................................................0.012g L-Histidine........................................................8.0mg L-Methionine ....................................................7.5mg Phenol Red.......................................................5.0mg L-Tryptophan ....................................................4.0mg Inositol .............................................................1.8mg Biotin ...............................................................1.0mg Calcium pantothenate ......................................1.0mg Choline chloride...............................................1.0mg Folic acid..........................................................1.0mg Nicotinamide....................................................1.0mg Pyridoxal·HCl ..................................................1.0mg Thiamine·HCl ..................................................1.0mg Riboflavin ........................................................0.1mg Serum ............................................50.0mL–100.0mL Glutamine solution.......................................... 6.0mL pH 7.2–7.4 at 25°C
Glutamine Solution: Composition per 100.0mL: L-Glutamine.........................................................5.0g
NaCl (0.85% solution) ................................ 100.0mL
Preparation of Glutamine Solution: Add the glutamine to the 0.85% NaCl solution. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except glutamine and serum, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.2–7.4 with 10% Na2CO3 solution. Filter sterilize. Aseptically add 6.0mL of sterile glutamine solution and 50.0–100.0mL of sterile serum. Human serum, bovine serum, horse serum, or fetal calf serum may be used. Mix thoroughly.
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Use: For the cultivation of mammalian cells in suspension.
Tissue Culture Tyrode Solution (TC Tyrode Solution) Composition per 1002.0mL: NaCl....................................................................8.0g Glucose ...............................................................1.0g NaHCO3 ..............................................................1.0g CaCl2·2H2O ........................................................0.2g KCl......................................................................0.2g MgCl2·6H2O .......................................................0.1g NaH2PO4 ...........................................................0.05g Phenol Red (1% solution)............................... 2.0mL pH 7.2–7.4 at 25°C
Preparation of Tissue Culture Tyrode Solution: Add components, except Phenol Red, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Add 2.0mL of Phenol Red solution. Adjust pH to 7.2–7.4. Filter sterilize.
Use: For use in tissue culture procedures.
Tissue Culture Vitamins Minimal Eagle, 100X (TC Vitamins Minimal Eagle, 100X) Composition per liter: Inositol .............................................................2.0mg Calcium pantothenate ......................................1.0mg Choline chloride...............................................1.0mg Folic acid .........................................................1.0mg Nicotinamide....................................................1.0mg Pyridoxal..........................................................1.0mg Thiamine·HCl ..................................................1.0mg Riboflavin ........................................................0.1mg pH 7.2–7.4 at 25°C
Preparation of TC Vitamins, Minimal Eagle 100X: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
Use: For the preparation of TC minimal medium Eagle used in tissue culture procedures.
T1N0 Broth (Tryptone Broth) Composition per liter: Pancreatic digest of casein................................10.0g pH 7.1 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling.
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T1N1 Agar
Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of Vibrio cholerae and other Vibrio species.
T1N1 Agar (Tryptone Salt Agar) Composition per liter: Agar ..................................................................20.0g NaCl ..................................................................10.0g Pancreatic digest of casein................................10.0g pH 7.1 ± 0.2 at 25°C
Preparation of Medium: Add components to
Use: For the cultivation of Vibrio cholerae and other Vibrio species.
T1N3 Broth (Tryptone Salt Broth) Composition per liter: NaCl..................................................................30.0g Pancreatic digest of casein................................10.0g pH 7.1 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes. Allow tubes to cool in a slanted position.
Use: For the cultivation of Vibrio cholerae and other
Use: For the cultivation of Vibrio cholerae and other
Composition per liter:
Vibrio species.
T1N2 Agar (Tryptone Salt Agar) Composition per liter: Agar ..................................................................20.0g NaCl ..................................................................20.0g Pancreatic digest of casein................................10.0g pH 7.1 ± 0.2 at 25°C
Vibrio species.
T1N6 Broth (Tryptone Salt Broth) NaCl..................................................................60.0g Pancreatic digest of casein................................10.0g pH 7.1 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of Vibrio cholerae and other Vibrio species.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes. Allow tubes to cool in a slanted position.
Use: For the cultivation of Vibrio cholerae and other Vibrio species.
T1N1 Broth (Tryptone Salt Broth)
T1N8 Broth (Tryptone Salt Broth) Composition per liter: NaCl..................................................................80.0g Pancreatic digest of casein................................10.0g pH 7.1 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Composition per liter:
Use: For the cultivation of Vibrio cholerae and other
NaCl ..................................................................10.0g Pancreatic digest of casein................................10.0g pH 7.1 ± 0.2 at 25°C
Vibrio species.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
T1N10 Broth (Tryptone Salt Broth) Composition per liter: NaCl................................................................100.0g Pancreatic digest of casein................................10.0g pH 7.1 ± 0.2 at 25°C
Todd-Hewitt Broth, Modified Preparation of Medium: Add components to
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distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Glucose ...............................................................2.0g NaHCO3 ..............................................................2.0g NaCl....................................................................2.0g Na2HPO4 .............................................................0.4g pH 7.8 ± 0.2 at 25°C
Use: For the cultivation of Vibrio cholerae and other
Source: This medium is available as a premixed
Vibrio species.
TOC Agar (Tween 80 Oxgall Caffeic Acid Agar) Composition per liter:
powder from Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 10 min at 10 psi pressure–115°C.
Agar ..................................................................20.0g Oxgall................................................................10.0g Caffeic acid .........................................................0.3g Tween 80....................................................... 10.0mL
Use: For the cultivation of group A streptococci
Source: This medium is available as a prepared me-
Todd-Hewitt Broth (ATCC Medium 235)
dium from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes.
Use: For the differentiation and identification of Candida albicans and Cryptococcus neoformans. Cryptococcus albicans produces germ tubes and chlamydospores when grown on this medium. Cryptococcus neoformans appears as tan to brown colonies.
Todd-Hewitt Broth Composition per liter: Beef heart, infusion from ................................500.0g Neopeptone .......................................................20.0g Na2CO3 ...............................................................2.5g Glucose ...............................................................2.0g NaCl ....................................................................2.0g Na2HPO4 .............................................................0.4g pH 7.8 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of group A streptococci used in serological typing, and for the cultivation of a variety of pathogenic microorganisms.
Todd-Hewitt Broth Composition per liter: Pancreatic digest of casein................................20.0g Infusion from 450.0g fat-free minced meat ......10.0g
used in serological typing, and for the cultivation of a variety of pathogenic microorganisms.
Composition per liter: Peptone .............................................................20.0g Beef heart, solids from infusion..........................3.1g Na2CO3 ...............................................................2.5g Glucose ...............................................................2.0g NaCl....................................................................2.0g Na2HPO4 .............................................................0.4g pH 7.8 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of Group A streptococci used in serological typing, and for the cultivation of a variety of pathogenic microorganisms.
Todd-Hewitt Broth, Modified Composition per liter: Neopeptone .......................................................20.0g Glucose ...............................................................2.0g NaHCO3 ..............................................................2.0g NaCl....................................................................2.0g Na2HPO4 .............................................................0.4g Beef heart infusion............................................. 1.0L pH 7.8 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 10 min at 10 psi pressure–115°C.
Use: For the cultivation of streptococci for serological identification.
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Toluidine Blue DNA Agar
Toluidine Blue DNA Agar Composition per liter: Agar ..................................................................10.0g NaCl ..................................................................10.0g Tris(hydroxymethyl)aminomethane buffer.........6.1g Deoxyribonucleic acid ........................................0.3g Toluidine Blue O.............................................0.083g CaCl2, anhydrous .............................................1.1mg pH 9.0 ± 0.2 at 25°C
Preparation of Medium: Add tris(hydroxymethyl)aminomethane buffer to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 9.0. Add the remaining components, except Toluidine Blue O. Mix thoroughly. Gently heat and bring to boiling. Add Toluidine Blue O. Mix thoroughly. If used the same day, sterilization is not necessary. Cool to 50°C. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation and differentiation of Staphylococcus aureus.
Toluidine Blue DNA Agar
MgSO4 ................................................................0.1g Lysine..............................................................0.058g Isoleucine........................................................0.052g Leucine ...........................................................0.052g Phenol Red......................................................0.050g Threonine........................................................0.048g Valine ..............................................................0.046g Tyrosine ..........................................................0.036g Phenylalanine..................................................0.032g Histidine..........................................................0.031g L-Cystine.........................................................0.024g Methionine......................................................0.015g Tryptophan......................................................0.010g Inositol .............................................................2.0mg Choline.............................................................1.0mg Folic acid .........................................................1.0mg Nicotinamide....................................................1.0mg Pantothenic acid...............................................1.0mg Pyridoxal·HCl ..................................................1.0mg Thiamine·HCl ..................................................1.0mg Riboflavin ........................................................0.1mg Fetal bovine serum, heat inactivated .......... 100.0mL pH 7.2–7.4 at 25°C
Composition per liter:
Preparation of Medium: Add components, ex-
Agar ..................................................................10.0g NaCl ..................................................................10.0g Tris(hydroxymethyl)aminomethane buffer.........6.1g Deoxyribonucleic acid (DNA)............................0.3g Toluidine Blue O.............................................0.083g CaCl2, anhydrous .............................................1.1mg pH 7.3 ± 0.2 at 25°C
cept fetal bovine serum, to distilled/deionized water and bring volume to 905.0mL. Mix thoroughly. Adjust pH to 7.2–7.4. Autoclave for 15 min at 15 psi pressure–121°C. Aseptically add 100.0mL of sterile, heat-inactivated fetal bovine serum. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation of Toxoplasma gondii.
Preparation of Medium: Add components, except Toluidine Blue O, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Add Toluidine Blue O. Mix thoroughly. Medium does not have to be sterilized if used immediately. Pour into sterile Petri dishes or distribute into sterile tubes. Allow tubes to cool in a slanted position.
Use: For the cultivation and differentiation of bacteria based on their production of deoxyribonuclease (DNase). Bacteria that produce DNase turn the medium pink.
Toxoplasma Medium Composition per liter: NaCl ....................................................................6.8g NaHCO3 ..............................................................2.2g Glucose ...............................................................1.0g KCl......................................................................0.4g Glutamine........................................................0.292g CaCl2 ...................................................................0.2g NaH2PO4·H2O.................................................0.125g Arginine ..........................................................0.105g
TPEY Agar (Tellurite Polymyxin Egg Yolk Agar) Composition per liter: NaCl..................................................................20.0g Agar ..................................................................15.5g Pancreatic digest of casein................................10.0g Yeast extract........................................................5.0g D-Mannitol ..........................................................5.0g LiCl .....................................................................2.0g Egg yolk emulsion (30% solution) ............. 100.0mL Chapman tellurite solution............................ 10.0mL Polymyxin B solution ..................................... 0.4mL pH 7.1 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Egg Yolk Emulsion (30% Solution): Composition per 100.0mL: NaCl....................................................................0.6g Egg yolk........................................................ 30.0mL
Preparation of Egg Yolk Emulsion (30% Solution): Add NaCl and egg yolk to distilled/deion-
Transgrow Medium ized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Chapman Tellurite Solution: Composition per 100.0mL: K2TeO3 ................................................................1.0g
Preparation of Chapman Tellurite Solution: Add K2TeO3 to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Polymyxin B Solution: Composition per 100.0mL: Polymyxin B .......................................................1.0g
Preparation of Polymyxin B Solution: Add polymyxin B to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Caution: Potassium tellurite is toxic. Preparation of Medium: Add components—except 30% egg yolk emulsion, Chapman tellurite solution, and polymyxin B solution—to distilled/ deionized water and bring volume to 890.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 100.0mL of sterile 30% egg yolk emulsion, 10.0mL of sterile Chapman tellurite solution, and 0.4mL of sterile polymyxin B solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the recovery of staphylococci.
TPGY Medium (Thioglycolate Peptone Glucose Yeast Extract Medium) Composition per liter: Pancreatic digest of casein................................50.0g Peptone................................................................5.0g Yeast extract........................................................5.0g Glucose ...............................................................1.0g Sodium thioglycolate ..........................................1.0g pH 7.1 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of a variety of anaerobic bacteria.
Trace Elements Solution HO-LE Composition per liter: H3BO3 ...............................................................2.85g MnCl2·4H2O .......................................................1.8g Sodium tartrate..................................................1.77g
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FeSO4·7H2O......................................................1.36g CoCl2·6H2O ......................................................0.04g CuCl2·2H2O.....................................................0.027g Na2MoO4·2H2O ..............................................0.025g ZnCl2 .................................................................0.02g
Preparation of Trace Elements Solution HOLE: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
Use: For the enrichment of other media requiring added trace metals.
Transgrow Medium Composition per liter: GC agar base............................................... 730.0mL Hemoglobin solution .................................. 250.0mL Vitox supplement .......................................... 10.0mL VCN antibiotic solution................................ 10.0mL pH 7.3 ± 0.2 at 25°C
GC Agar Base: Composition per 730.0mL: Special peptone.................................................15.0g Agar ..................................................................20.0g NaCl....................................................................5.0g K2HPO4...............................................................4.0g Cornstarch...........................................................1.0g KH2PO4...............................................................1.0g pH 7.2 ± 0.2 at 25°C
Preparation of GC Agar Base: Add components of GC medium base and the hemoglobin to distilled/deionized water and bring volume to 730.0mL. Mix thoroughly. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°– 50°C.
Hemoglobin Solution: Composition per 250.0mL: Hemoglobin ........................................................5.0g
Preparation of Hemoglobin Solution: Add hemoglobin to distilled/deionized water and bring volume to 250.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Vitox Supplement: Composition per 10.0mL: Glucose ...............................................................2.0g L-Cysteine·HCl ...............................................0.518g L-Glutamine ........................................................0.2g L-Cystine.........................................................0.022g Adenine sulfate .................................................0.01g Nicotinamide adenine dinucleotide .................5.0mg Cocarboxylase..................................................2.0mg Guanine·HCl ....................................................0.6mg Fe(NO3)3·6H2O................................................0.4mg p-Aminobenzoic acid.....................................0.26mg
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Transgrow Medium
Vitamin B12 ......................................................0.2mg Thiamine·HCl ................................................0.06mg
Supplement B: Composition per 10.0mL:
Preparation of Vitox Supplement: Add com-
Supplement B contains yeast concentrate, glutamine, coenzyme, cocarboxylase, hematin, and growth factors.
ponents to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
VCN Antibiotic Solution: Composition per 10.0mL: Colistin methane sulfonate...............................7.5mg Vancomycin .....................................................3.0mg Nystatin........................................................12,500U
Preparation of VCN Antibiotic Solution: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: To 730.0mL of cooled, sterile GC agar base, aseptically add 250.0mL of sterile hemoglobin solution, 10.0mL of sterile Vitox supplement, and 10.0mL of VCN antibiotic solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes. Use: For the cultivation and transport of fastidious microorganisms, especially Neisseria species.
Transgrow Medium Composition per liter: GC medium base......................................... 730.0mL Hemoglobin solution................................... 250.0mL Supplement B................................................ 10.0mL VCNT antibiotic solution.............................. 10.0mL pH 7.3 ± 0.2 at 25°C
GC Medium Base: Composition per 730.0mL: Proteose peptone no. 3 ......................................15.0g Agar ..................................................................20.0g NaCl ....................................................................5.0g K2HPO4 ...............................................................4.0g Glucose ...............................................................1.5g Cornstarch...........................................................1.0g KH2PO4 ...............................................................1.0g pH 7.2 ± 0.2 at 25°C
Preparation of GC Medium Base: Add components to distilled/deionized water and bring volume to 730.0mL. Mix thoroughly. Gently heat until boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Hemoglobin Solution: Composition per 250.0mL: Hemoglobin ......................................................10.0g
Preparation of Hemoglobin Solution: Add hemoglobin to distilled/deionized water and bring volume to 250.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Preparation of Supplement B: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. Source: Supplement B is available as a premixed powder from BD Diagnostic Systems. VCNT Antibiotic Solution: Composition per 10.0mL: Colistin methane sulfonate ..............................7.5mg Trimethoprim lactate........................................5.0mg Vancomycin .....................................................3.0mg Nystatin........................................................ 12,500U
Preparation of VCNT Antibiotic Solution: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: To 730.0mL of cooled, sterile GC medium base, aseptically add 250.0mL of sterile hemoglobin solution, 10.0mL of sterile supplement B, and 10.0mL of VCNT antibiotic solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation and transport of fastidious microorganisms, especially Neisseria species.
Transgrow Medium with Trimethoprim Composition per liter: Agar ..................................................................20.0g Hemoglobin ......................................................10.0g Pancreatic digest of casein..................................7.5g Selected meat peptone ........................................7.5g NaCl....................................................................5.0g K2HPO4...............................................................4.0g Glucose ...............................................................1.5g Cornstarch...........................................................1.0g KH2PO4...............................................................1.0g Supplement solution ..................................... 10.0mL VCNT inhibitor............................................. 10.0mL pH 6.7 ± 0.2 at 25°C
Source: This medium is available as a prepared medium from BD Diagnostic Systems.
Supplement Solution: Composition per liter: Glucose ...........................................................100.0g L-Cysteine·HCl..................................................25.9g L-Glutamine ......................................................10.0g L-Cystine .............................................................1.1g Adenine...............................................................1.0g
Transport Medium Nicotinamide adenine dinucleotide ..................0.25g Vitamin B12 .........................................................0.1g Thiamine pyrophosphate.....................................0.1g Guanine·HCl .....................................................0.03g Fe(NO3)3·6H2O .................................................0.02g p-Aminobenzoic acid......................................0.013g Thiamine·HCl ..................................................3.0mg
Source: The supplement solution (IsoVitaleX enrichment) is available from BD Diagnostic Systems. This enrichment may be replaced by supplement VX from BD Diagnostic Systems.
Preparation of Supplement Solution: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
VCNT Inhibitor: Composition per 10.0mL: Colistin.............................................................7.5mg Trimethoprim lactate........................................5.0mg Vancomycin .....................................................3.0mg Nystatin........................................................12,500U
Preparation of VCNT Inhibitor: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except supplement solution and VCNT inhibitor, to distilled/deionized water and bring volume to 980.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C under 5–30% CO2. Aseptically add 10.0mL of sterile supplement solution and 10.0mL of sterile VCNT inhibitor. Mix thoroughly. Aseptically distribute under 5–30% CO2 into sterile screwcapped tubes.
Use: For the transportation and recovery of pathogenic Neisseria species.
Transgrow Medium without Trimethoprim Composition per liter: Agar ..................................................................20.0g Hemoglobin ......................................................10.0g Pancreatic digest of casein..................................7.5g Selected meat peptone ........................................7.5g NaCl ....................................................................5.0g K2HPO4 ...............................................................4.0g Glucose ...............................................................1.5g Cornstarch...........................................................1.0g KH2PO4 ...............................................................1.0g Supplement solution ..................................... 10.0mL VCN inhibitor ............................................... 10.0mL pH 6.7 ± 0.2 at 25°C
435
Source: This medium is available as a prepared medium from BD Diagnostic Systems. Supplemement Solution: Composition per liter: Glucose ...........................................................100.0g L-Cysteine·HCl..................................................25.9g L-Glutamine ......................................................10.0g L-Cystine .............................................................1.1g Adenine...............................................................1.0g Nicotinamide adenine dinucleotide ..................0.25g Vitamin B12 .........................................................0.1g Thiamine pyrophosphate ....................................0.1g Guanine·HCl .....................................................0.03g Fe(NO3)3·6H2O.................................................0.02g p-Aminobenzoic acid......................................0.013g Thiamine·HCl ..................................................3.0mg
Source: The supplement solution IsoVitaleX enrichment is available from BD Diagnostic Systems. This enrichment may be replaced by supplement VX from BD Diagnostic Systems.
Preparation of Supplement Solution: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
VCN Inhibitor: Composition per 10.0mL: Colistin.............................................................7.5mg Vancomycin .....................................................3.0mg Nystatin........................................................ 12,500U
Preparation of VCN Inhibitor: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except supplement solution and VCN inhibitor, to distilled/deionized water and bring volume to 980.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C under 5–30% CO2. Aseptically add 10.0mL of sterile supplement solution and 10.0mL of sterile VCN inhibitor. Mix thoroughly. Aseptically distribute under 5–30% CO2 into sterile screwcapped tubes.
Use: For the transportation and recovery of pathogenic Neisseria species.
Transport Medium Composition per liter: Sodium glycerophosphate.................................10.0g Agar ....................................................................3.0g Sodium thioglycolate ..........................................1.0g CaCl2·2H2O ........................................................0.1g Methylene Blue................................................2.0mg pH 7.3 ± 0.2 at 25°C
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Transport Medium Stuart
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
ing. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Preparation of Medium: Add components to
Brain Heart Infusion Broth: Composition per liter:
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Distribute into screw-capped tubes or vials. Fill tubes nearly to capacity. Leave only enough space so that when a small swab is introduced the tube does not overflow. Autoclave for 10 min at 15 psi pressure–121°C. Tighten caps on tubes.
Use: For the transportation of swab specimens for the recovery of a wide variety of microorganisms, including Neisseria gonorrhoeae.
Transport Medium Stuart Composition per liter: Sodium glycerophosphate.................................10.0g Agar ....................................................................3.0g Sodium thioglycolate ..........................................0.9g CaCl2·2H2O.........................................................0.1g Methylene Blue................................................2.0mg pH 7.3 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Distribute into screw-capped tubes or vials. Fill tubes nearly to capacity. Leave only enough space so that when a small swab is introduced the tube does not overflow. Autoclave for 10 min at 15 psi pressure–121°C. Tighten caps on tubes.
Use: For the transportation of swab specimens for the recovery of a wide variety of microorganisms, including Neisseria gonorrhoeae.
Treponema Isolation Medium Composition per liter: Solution A ................................................... 450.0mL Spirolate broth............................................. 450.0mL Rabbit serum, inactivated at 56°C for 30 min ............. 100.0mL pH 7.4 ± 0.2 at 25°C
Solution A: Composition per 450.0mL: Agar ....................................................................8.0g Asparagine ........................................................0.25g Sodium thioglycolate ........................................0.25g Pancreatic digest of casein................................0.25g Brain heart infusion broth ........................... 450.0mL
Preparation of Solution A: Combine components. Mix thoroughly. Gently heat and bring to boil-
Pancreatic digest of gelatin...............................14.5g Brain heart, solids from infusion ........................6.0g Peptic digest of animal tissue .............................6.0g NaCl....................................................................5.0g Casein .................................................................5.0g Glucose ...............................................................3.0g Na2HPO4 .............................................................2.5g
Preparation of Brain Heart Infusion Broth: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly.
Spirolate Broth: Composition per liter: Pancreatic digest of casein................................15.0g Glucose ...............................................................5.0g Yeast extract........................................................5.0g NaCl....................................................................2.5g L-Cysteine·HCl·H2O............................................1.0g Sodium thioglycolate ..........................................0.5g Palmitic acid .....................................................0.05g Stearic acid........................................................0.05g Oleic acid ..........................................................0.05g Linoleic acid .....................................................0.05g
Preparation of Spirolate Broth: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C.
Preparation of Medium: Combine 450.0mL of sterile solution A, 450.0mL of sterile spirolate broth, and 100.0mL of rabbit serum. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the isolation and cultivation of oral, genital, and fecal treponemes.
Treponema Isolation Medium Composition per liter: Beef heart, solids from infusion........................20.0g Ionagar no. 2 .......................................................7.2g K2HPO4...............................................................2.0g Arabinose............................................................0.8g Glucose ...............................................................0.8g Maltose ...............................................................0.8g Polypeptone ........................................................0.8g Pyruvate ..............................................................0.8g Starch, soluble.....................................................0.8g Sucrose................................................................0.8g Cysteine·HCl.....................................................0.68g (NH4)2SO4 ..........................................................0.6g Serine ..................................................................0.4g
Treponema Medium Tryptose ..............................................................0.4g Yeast extract........................................................0.4g NaCl ....................................................................0.2g Rumen fluid ................................................ 500.0mL Rabbit serum–cocarboxylase solution ........ 100.0mL pH 7.2 ± 0.2 at 25°C
Rabbit Serum-Cocarboxylase Solution: Composition per liter: Rabbit serum, heat inactivated.................... 100.0mL Cocarboxylase solution................................... 1.0mL
Preparation of Rabbit Serum-Cocarboxylase Solution: Heat rabbit serum at 56°C for 1h. Add 1.0mL of cocarboxylase solution. Mix thoroughly.
Cocarboxylase Solution: Composition per 1.0mL: Cocarboxylase.....................................................0.5g
Preparation of Cocarboxylase Solution: Add cocarboxylase to 1.0mL of distilled/deionized water. Mix thoroughly. Filter sterilize. Preparation of Medium: Add components, except rumen fluid and rabbit serum-cocarboxylase solution, to distilled/deionized water and bring volume to 400.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C. Aseptically add 500.0mL of sterile rumen fluid and 100.0mL of sterile rabbit serum–cocarboxylase solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation of oral treponemes.
Treponema Medium Composition per liter: Pancreatic digest of casein................................30.0g Ionagar no. 2 .......................................................8.0g Glucose ...............................................................5.0g Yeast extract........................................................5.0g NaCl ....................................................................2.5g Cysteine·HCl.....................................................0.75g Horse serum, inactivated............................. 100.0mL pH 7.4 ± 0.2 at 25°C
437
Treponema Medium Composition per liter: Spirolate agar .............................................. 900.0mL Rabbit serum, inactivated at 56°C for 30 min ............. 100.0mL
Spirolate Agar: Composition per liter: Pancreatic digest of casein................................15.0g Agar ..................................................................14.0g Glucose ...............................................................5.0g Yeast extract........................................................5.0g NaCl....................................................................2.5g L-Cysteine·HCl·H2O............................................1.0g Sodium thioglycolate ..........................................0.5g Palmitic acid .....................................................0.05g Stearic acid........................................................0.05g Oleic acid ..........................................................0.05g Linoleic acid .....................................................0.05g
Preparation of Spirolate Agar: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C.
Preparation of Medium: To 900.0mL of cooled, sterile spirolate agar, aseptically add 100.0mL of rabbit serum. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the isolation of oral treponemes.
Treponema Medium Composition per liter: Spirolate agar .............................................. 675.0mL Brain heart infusion broth........................... 225.0mL Rabbit serum, inactivated at 56°C for 30 min ............. 100.0mL pH 7.0–7.2 ± 0.2 at 25°C
Spirolate Agar: Composition per 675.0mL:
cept horse serum, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 100.0mL of sterile horse serum. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Pancreatic digest of casein................................15.0g Ionagar no. 2 .......................................................8.0g Glucose ...............................................................5.0g Yeast extract........................................................5.0g NaCl....................................................................2.5g L-Cysteine·HCl·H2O............................................1.0g Sodium thioglycolate ..........................................0.5g Palmitic acid .....................................................0.05g Stearic acid........................................................0.05g Oleic acid ..........................................................0.05g Linoleic acid .....................................................0.05g
Use: For the isolation and cultivation of oral tre-
Preparation of Spirolate Agar: Add compo-
ponemes.
nents to distilled/deionized water and bring volume
Preparation of Medium: Add components, ex-
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Treponema Medium
to 675.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Spirolate Broth: Composition per liter:
Brain Heart Infusion Broth: Composition per liter: Pancreatic digest of gelatin ...............................14.5g Brain heart, solids from infusion ........................6.0g Peptic digest of animal tissue..............................6.0g NaCl ....................................................................5.0g Casein..................................................................5.0g Glucose ...............................................................3.0g Na2HPO4 .............................................................2.5g
Pancreatic digest of casein................................15.0g Glucose ...............................................................5.0g Yeast extract........................................................5.0g NaCl....................................................................2.5g L-Cysteine·HCl·H2O............................................1.0g Sodium thioglycolate ..........................................0.5g Palmitic acid .....................................................0.05g Stearic acid........................................................0.05g Oleic acid ..........................................................0.05g Linoleic acid .....................................................0.05g
Preparation of Brain Heart Infusion Broth:
Preparation of Spirolate Broth: Add compo-
Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly.
Preparation of Medium: Aseptically combine 675.0mL of cooled, sterile spirolate agar, 225.0mL of cooled, sterile brain heart infusion broth, and 100.0mL of rabbit serum. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation of oral treponemes.
Treponema Medium Composition per liter: Solution A ................................................... 440.0mL Spirolate broth............................................. 440.0mL Rabbit serum, inactivated at 56°C for 30 min ............. 100.0mL Mucin solution .............................................. 20.0mL pH 7.8 ± 0.2 at 25°C
Solution A: Composition per 440.0mL: Ionagar no. 2 .......................................................8.0g Brain heart infusion broth ........................... 440.0mL
Brain Heart Infusion Broth: Composition per liter: Pancreatic digest of gelatin ...............................14.5g Brain heart, solids from infusion ........................6.0g Peptic digest of animal tissue..............................6.0g NaCl ....................................................................5.0g Casein..................................................................5.0g Glucose ...............................................................3.0g Na2HPO4 .............................................................2.5g
Preparation of Brain Heart Infusion Broth: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly.
Preparation of Solution A: Add 8.0g of ionagar to 440.0mL of brain heart infusion broth. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
nents to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°.
Mucin Solution: Composition per 20.0mL: Mucin..................................................................0.2g
Preparation of Mucin Solution: Add mucin to distilled/deionized water and bring volume to 20.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Aseptically combine 440.0mL of solution A, 440.0mL of spirolate broth, 100.0mL of rabbit serum, and 20.0mL of mucin solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the isolation of intestinal treponemes.
Treponema Medium Composition per liter: Agar ..................................................................13.0g Glucose ...............................................................1.4g Cysteine·HCl.....................................................0.64g (NH4)2SO4 ..........................................................0.5g Polypeptone ........................................................0.5g Starch, soluble.....................................................0.5g Yeast extract........................................................0.5g Resazurin .........................................................1.6mg Salts solution............................................... 500.0mL Bovine rumen fluid ..................................... 280.0mL pH 7.2–7.5 at 25°C
Salts Solution: Composition per liter: NaHCO3 ............................................................10.0g NaCl....................................................................2.0g K2HPO4...............................................................1.0g KH2PO4...............................................................1.0g CaCl2 ...................................................................0.2g MgSO4 ................................................................0.2g CoCl.................................................................3.4mg
Treponema Medium MnSO4 .............................................................3.4mg NaMoO4 ...........................................................3.4mg
Preparation of Salts Solution: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly.
Preparation of Medium: Add components, except bovine rumen fluid, to distilled/deionized water and bring volume to 720.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add bovine rumen fluid. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation of intestinal treponemes.
Treponema Medium Composition per liter: Cysteine·HCl·H2O...............................................1.0g Glucose ...............................................................1.0g Nicotinamide.......................................................0.4g Spermidine·4HCl ..............................................0.15g Sodium isobutyrate ...........................................0.02g Thiamine pyrophosphate..................................5.0mg PPLO broth ................................................. 900.0mL Rabbit serum, inactivated ........................... 100.0mL pH 7.8 ± 0.2 at 25°C
PPLO Broth: Composition per 900.0mL: Beef heart, infusion from solids........................50.0g Peptone..............................................................10.0g NaCl ....................................................................5.0g
Preparation of PPLO Broth: Add components to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly.
Preparation of Medium: Combine components, except rabbit serum. Mix thoroughly. Filter sterilize. Aseptically add sterile rabbit serum. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation of oral treponemes. For the cultivation of Treponema denticola, Treponema macrodentium, and Treponema oralis.
Treponema Medium Composition per liter: Spirolate broth............................................. 675.0mL Brain heart infusion broth ........................... 225.0mL Rabbit serum ............................................... 100.0mL
Spirolate Broth: Composition per liter: Pancreatic digest of casein................................15.0g Glucose ...............................................................5.0g Yeast extract........................................................5.0g
439
NaCl....................................................................2.5g L-Cysteine·HCl·H2O............................................1.0g Sodium thioglycolate ..........................................0.5g Palmitic acid .....................................................0.05g Stearic acid........................................................0.05g Oleic acid ..........................................................0.05g Linoleic acid .....................................................0.05g
Preparation of Spirolate Broth: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C.
Brain Heart Infusion Broth: Composition per liter: Pancreatic digest of gelatin...............................14.5g Brain heart, solids from infusion ........................6.0g Peptic digest of animal tissue .............................6.0g NaCl....................................................................5.0g Casein .................................................................5.0g Glucose ...............................................................3.0g Na2HPO4 .............................................................2.5g
Preparation of Brain Heart Infusion Broth: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C.
Preparation of Medium: Aseptically combine 675.0mL of cooled, sterile spirolate broth, 225.0mL of cooled, sterile brain heart infusion broth, and 100.0mL of rabbit serum. Mix thoroughly.
Use: For the cultivation of oral treponemes.
Treponema Medium Composition per liter: Heart infusion broth, modified ................... 450.0mL Spirolate broth ............................................ 450.0mL Rabbit serum, inactivated ........................... 100.0mL pH 7.4 ± 0.2 at 25°C
Heart Infusion Broth, Modified: Composition per liter: Beef heart, solids from infusion......................500.0g Tryptose ............................................................10.0g NaCl....................................................................5.0g Asparagine ..........................................................2.5g Sodium thioglycolate ..........................................2.5g Pancreatic digest of casein..................................2.5g
Preparation of Heart Infusion Broth, Modified: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C.
Spirolate Broth: Composition per liter: Pancreatic digest of casein................................15.0g
440
Treponema Medium
Glucose ...............................................................5.0g Yeast extract........................................................5.0g NaCl ....................................................................2.5g L-Cysteine·HCl·H2O............................................1.0g Sodium thioglycolate ..........................................0.5g Palmitic acid .....................................................0.05g Stearic acid........................................................0.05g Oleic acid ..........................................................0.05g Linoleic acid .....................................................0.05g
Preparation of Spirolate Broth: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C.
Preparation of Medium: Aseptically combine 450.0mL of cooled, sterile spirolate broth, 450.0mL of cooled, sterile heart infusion broth, modified, and 100.0mL of rabbit serum. Mix thoroughly. Aseptically distribute into sterile tubes or flasks. Use: For the cultivation of treponemes.
Treponema Medium Composition per 500.0mL: Beef heart, solids from infusion......................250.0g Sucrose..............................................................50.0g Tryptose ..............................................................5.0g NaCl ....................................................................2.5g Yeast extract........................................................2.5g Agar ....................................................................0.5g Sodium thioglycolate ........................................0.38g MgSO4 ..............................................................0.05g Horse serum, inactivated............................. 100.0mL pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components, except horse serum, to distilled/deionized water and bring volume to 400.0mL. Mix thoroughly. Adjust pH to 7.4. Gently heat and bring to boiling. Distribute into tubes in 4.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C. Prior to inoculation, add 1.0mL sterile horse serum to each tube.
Use: For the cultivation and maintenance of Treponema pallidum and other Treponema species.
Treponema Medium 1 Composition per liter: Thioglycolate agar USP, alternate............... 900.0mL Normal calf serum ...................................... 100.0mL pH 7.1 ± 0.2 at 25°C
Thioglycolate Agar USP, Alternate: Composition per 900.0mL: Pancreatic digest of casein................................15.0g Ionagar no. 2 .......................................................7.0g
Glucose ...............................................................5.5g Yeast extract........................................................5.0g NaCl....................................................................2.5g L-Cystine .............................................................0.5g Sodium thioglycolate ..........................................0.5g
Preparation of Thioglycolate Agar USP, Alternate: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Preparation of Medium: Aseptically combine 900.0mL of cooled sterile thioglycolate agar USP, alternate, and 100.0mL of calf serum. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation of treponemes.
Treponema Medium 2 Composition per liter: Pancreatic digest of casein................................30.0g Ionagar no. 2 .......................................................7.0g Glucose ...............................................................5.0g Yeast extract........................................................5.0g NaCl....................................................................2.5g L-Cysteine·HCl·H2O............................................2.0g Rabbit serum............................................... 100.0mL pH 7.2 ± 0.2 at 25°C
Preparation of Medium: Add components, except rabbit serum, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile rabbit serum. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation of treponemes.
Treponema Medium 3 Composition per liter: Spirolate agar .............................................. 675.0mL Brain heart infusion broth........................... 225.0mL Rabbit serum............................................... 100.0mL
Spirolate Agar: Composition per liter: Pancreatic digest of casein................................15.0g Ionagar no. 2 .......................................................7.0g Glucose ...............................................................5.0g Yeast extract........................................................5.0g NaCl....................................................................2.5g L-Cysteine·HCl·H2O............................................1.0g Sodium thioglycolate ..........................................0.5g Palmitic acid .....................................................0.05g
Trichomonas Medium No. 2
441
Stearic acid........................................................0.05g Oleic acid ..........................................................0.05g Linoleic acid .....................................................0.05g
Preparation of Salts Solution: Add components
Preparation of Spirolate Agar: Add compo-
Preparation of Medium: Add components, ex-
nents to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 25°C.
cept bovine rumen fluid, to distilled/deionized water and bring volume to 720.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 280.0mL of sterile bovine rumen fluid. Mix thoroughly. Aseptically and anaerobically distribute into sterile tubes or flasks under 100% N2.
Brain Heart Infusion Broth: Composition per liter: Pancreatic digest of gelatin ...............................14.5g Brain heart, solids from infusion ........................6.0g Peptic digest of animal tissue..............................6.0g NaCl ....................................................................5.0g Casein..................................................................5.0g Glucose ...............................................................3.0g Na2HPO4 .............................................................2.5g
Preparation of Brain Heart Infusion Broth: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C.
to distilled/deionized water and bring volume to 1.0L. Mix thoroughly.
Use: For the cultivation of fecal and intestinal treponemes.
Trichomonas Medium Composition per liter: Liver digest .......................................................25.0g NaCl....................................................................6.5g Glucose ...............................................................5.0g Agar ....................................................................1.0g Horse serum .................................................. 80.0mL pH 6.4 ± 0.2 at 25°C
Preparation of Medium: Aseptically combine 675.0mL of cooled, sterile spirolate broth, 225.0mL of cooled, sterile brain heart infusion broth, and 100.0mL of rabbit serum. Mix thoroughly.
Source: This medium is available as a premixed
Use: For the cultivation of treponemes.
Horse serum .................................................. 80.0mL
powder from Oxoid Unipath.
Horse Serum: Composition per 80.0mL: Preparation of Horse Serum: Gently heat ster-
Treponema Medium, Prereduced Composition per liter:
ile horse serum to 56°C for 30 min. Aseptically adjust pH to 6.0 with 0.1N HCl. Use immediately.
Agar ....................................................................1.6g Glucose ...............................................................1.4g Cysteine·HCl·H2O.............................................0.64g (NH4)2SO4...........................................................0.5g Polypeptone ........................................................0.5g Starch, soluble.....................................................0.5g Yeast extract........................................................0.5g Resazurin .........................................................1.6mg Salts solution............................................... 500.0mL Bovine rumen fluid ..................................... 280.0mL pH 7.2–7.5 at 25°C
Preparation of Medium: Add components, ex-
Salts Solution: Composition per liter:
Composition per liter:
NaHCO3 ............................................................10.0g NaCl ....................................................................2.0g K2HPO4 ...............................................................1.0g KH2PO4 ...............................................................1.0g CaCl2 ...................................................................0.2g MgSO4 ................................................................0.2g CoCl .................................................................3.4mg MnSO4 .............................................................3.4mg NaMoO4 ...........................................................3.4mg
cept horse serum, to distilled/deionized water and bring volume to 920.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 80.0mL of freshly prepared sterile horse serum. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation of Trichomonas vaginalis.
Trichomonas Medium No. 2 Glucose .............................................................22.5g Liver digest .......................................................18.0g Pancreatic digest of casein................................17.0g NaCl....................................................................5.0g Pancreatic digest of soybean meal......................3.0g K2HPO4...............................................................2.5g Chloramphenicol.............................................0.125g Horse serum ................................................ 250.0mL Calcium pantothenate (0.5% solution) ........... 1.0mL pH 6.2 ± 0.2 at 25°C
442
Trichomonas Selective Medium
Source: This medium is available as a prepared medium from Oxoid Unipath.
Preparation of Medium: Add components, except horse serum, to distilled/deionized water and bring volume to 750.0mL. Mix thoroughly. Autoclave for 15 min at 5 psi pressure–108°C. Cool to 45°–50°C. Aseptically add 250.0mL of sterile horse serum. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the isolation of Trichomonas vaginalis.
Trichomonas Selective Medium Composition per liter: Liver digest .......................................................25.0g NaCl ....................................................................6.5g Glucose ...............................................................5.0g Agar ....................................................................1.0g Horse serum .................................................. 80.0mL Antibiotic inhibitor ....................................... 10.0mL pH 6.4 ± 0.2 at 25°C
Glucose ...............................................................5.0g Agar ....................................................................1.0g Horse serum .................................................. 80.0mL Antibiotic inhibitor ....................................... 10.0mL pH 6.4 ± 0.2 at 25°C
Horse Serum: Composition per 80.0mL: Horse serum .................................................. 80.0mL
Preparation of Horse Serum: Gently heat sterile horse serum to 56°C for 30 min. Aseptically adjust pH to 6.0 with 0.1N HCl. Use immediately.
Antibiotic Inhibitor: Composition per 10.0mL: Chloramphenicol..........................................100.0mg
Preparation of Antibiotic Inhibitor: Add chloramphenicol to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, ex-
Horse serum .................................................. 80.0mL
cept horse serum, to distilled/deionized water and bring volume to 910.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 80.0mL of freshly prepared sterile horse serum and 10.0mL of sterile antibiotic inhibitor. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Preparation of Horse Serum: Gently heat ster-
Use: For the cultivation of Trichomonas vaginalis
Source: This medium is available as a premixed powder from Oxoid Unipath.
Horse Serum: Composition per 80.0mL:
ile horse serum to 56°C for 30 min. Aseptically adjust pH to 6.0 with 0.1N HCl. Use immediately.
Antibiotic Inhibitor: Composition per 10.0mL: Streptomycin ................................................500.0mg Penicillin G .............................................1,000,000U
Preparation of Antibiotic Inhibitor: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except horse serum, to distilled/deionized water and bring volume to 910.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 80.0mL of freshly prepared sterile horse serum and 10.0mL of sterile antibiotic inhibitor. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation of Trichomonas vaginalis from specimens with a mixed bacterial flora.
Trichomonas Selective Medium Composition per liter: Liver digest .......................................................25.0g NaCl ....................................................................6.5g
from specimens with a mixed bacterial flora.
Trichosel™ Broth, Modified Composition per liter: Pancreatic digest of casein................................12.0g Yeast extract........................................................5.0g Liver extract........................................................2.0g Maltose ...............................................................2.0g L-Cysteine·HCl....................................................1.0g Agar ....................................................................1.0g Chloramphenicol.................................................0.1g Methylene Blue................................................3.0mg Horse serum .................................................. 50.0mL pH 6.0 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 13 psi pressure–118°C. Cool to 45°–50°C. Aseptically add 50.0mL of sterile horse serum. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the isolation and cultivation of Trichomonas species.
Trypaflavin Nalidixic Acid Serum Agar
Trimethylamine N-Oxide Medium (TMAO Medium) Composition per liter: Beef extract .......................................................10.0g Peptone..............................................................10.0g NaCl ....................................................................5.0g Agar ....................................................................2.0g Trimethylamine N-oxide.....................................1.0g Yeast extract........................................................1.0g pH 7.5 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into screw-capped tubes in 4.0mL volumes. Autoclave for 15 min at 15 psi pressure– 121°C. Allow tubes to cool in an upright position.
Use: For the cultivation and differentiation of Campylobacter. Campylobacter jejuni and Campylobacter coli will not grow.
Triple Sugar Iron Agar (TSI Agar) Composition per liter: Peptone..............................................................20.0g Agar ..................................................................12.0g Lactose ..............................................................10.0g Sucrose..............................................................10.0g NaCl ....................................................................5.0g Beef extract .........................................................3.0g Yeast extract........................................................3.0g Glucose ...............................................................1.0g Ferric citrate........................................................0.3g Na2S2O3 ..............................................................0.3g Phenol Red......................................................0.025g pH 7.4 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems and Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Allow tubes to cool in a slanted position to form a 1.0-inch butt.
Use: For the differentiation of members of the Enterobacteriaceae based on their fermentation of lactose, sucrose, and glucose and the production of H2S.
443
Triple Sugar Iron Agar (TSI Agar) Composition per liter: Agar ..................................................................13.0g Pancreatic digest of casein................................10.0g Peptic digest of animal tissue ...........................10.0g Lactose..............................................................10.0g Sucrose..............................................................10.0g NaCl....................................................................5.0g Glucose ...............................................................1.0g Fe(NH4)2(SO4)2·6H2O ........................................0.2g Na2S2O3 ..............................................................0.2g Phenol Red......................................................0.025g pH 7.3 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Allow tubes to cool in a slanted position to form a 1.0-inch butt.
Use: For the differentiation of members of the Enterobacteriaceae based on their fermentation of lactose, sucrose, and glucose and the production of H2S.
Trypaflavin Nalidixic Acid Serum Agar (TNSA Agar) Composition per liter: Ionagar no. 2 .....................................................12.0g Peptone .............................................................10.0g Beef extract.........................................................3.0g H2O ............................................................. 926.5mL Bovine serum, heat inactivated..................... 50.0mL Nalidixic acid solution.................................. 20.0mL Trypaflavin solution........................................ 3.5mL pH 7.2–7.4 at 25°C
Nalidixic Acid Solution: Composition per 10.0mL: Nalidixic acid....................................................0.02g
Preparation of Nalidixic Acid Solution: Add nalidixic acid to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. Trypaflavin Solution: Composition per 10.0mL: Trypaflavin..........................................................0.1g
Preparation of Trypaflavin Solution: Add trypaflavin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components—except bovine serum, nalidixic acid solution, and try-
444
Trypanosome Medium
paflavin solution—to distilled/deionized water and bring volume to 926.5mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 50.0mL of sterile bovine serum, 20.0mL of sterile nalidixic acid solution, and 3.5mL of trypaflavin solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation and cultivation of Listeria species from preenriched specimens.
Trypanosome Medium Composition per 1300.0mL: Solid phase......................................................... 1.0L Liquid phase (Locke’s solution) ................. 300.0mL pH 7.2–7.4 at 25°C
Solid Phase: Composition per liter: Agar ..................................................................15.0g NaCl ....................................................................8.0g Peptone................................................................5.0g Beef extract .........................................................3.0g Rabbit blood, defibrinated .......................... 300.0mL
Preparation of Solid Phase: Add components, except rabbit blood, to distilled/deionized water and bring volume to 700.0mL. Mix thoroughly. Adjust pH to 7.2–7.4. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Aseptically add 300.0mL of sterile defibrinated rabbit blood. Mix thoroughly. Distribute 10.0mL aliquots into sterile screw-capped tubes. Allow to solidify in a slanted position.
Liquid Phase (Locke's Solution): Composition per liter: NaCl ....................................................................8.0g Glucose ...............................................................2.5g KH2PO4 ...............................................................0.3g CaCl2 ...................................................................0.2g KCl......................................................................0.2g
Preparation of Liquid Phase (Locke’s Solution): Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C.
Preparation of Medium: Aseptically overlay agar slants (solid phase) with 3.0mL per tube of sterile liquid phase (Locke’s solution). Use: For the cultivation of Leishmania donovani, Leishmania braziliensis, Trypanosoma gambiense, and Trypanosoma rhodesiense.
NaCl....................................................................5.0g Glucose ...............................................................1.0g pH 7.6 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For use as a base medium to which enrichments are added. For the cultivation of fastidious microorganisms.
Tryptic Nitrate Medium Composition per liter: Tryptose ............................................................20.0g Na2HPO4 .............................................................2.0g Agar ....................................................................1.0g Glucose ...............................................................1.0g KNO3 ..................................................................1.0g pH 7.6 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes in 10.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation and differentiation of Pseudomonas and related genera. For the differentiation of bacteria based on their reduction of nitrate to nitrite. After incubation of the bacterium in tryptic nitrate medium for 18–24 hr, sulfanillic acid and αnaphthol reagents are added. Nitrate reduction is indicated by the development of a red to violet color.
Tryptic Soy Agar with Sodium Chloride (ATCC Medium 2276) Composition per liter: Pancreatic digest of casein................................50.0g NaCl..................................................................20.0g Agar ..................................................................15.0g Pancreatic digest of soybean meal......................5.0g MgSO4·7H2O ......................................................1.5g pH 7.3 ± 0.2 at 25°C
Preparation of Medium: Add components to
Composition per liter:
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Tryptic digest of beef heart ...............................10.0g
Use: For the cultivation of Vibrio species.
Tryptic Digest Broth
Trypticase Peptone Glucose Yeast Extract Broth
Tryptic Soy Fast Green Agar (TSFA) Composition per liter: Pancreatic digest of casein................................17.0g Agar ..................................................................15.0g NaCl ....................................................................5.0g Papaic digest of soybean meal ............................3.0g K2HPO4 ...............................................................2.5g Glucose ...............................................................2.5g Fast Green FCF.................................................0.25g pH 7.3 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically adjust pH to 7.3. Pour into sterile Petri dishes.
Use: For the isolation and cultivation of Salmonella species.
Trypticase Agar Base
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Use: For differentiation of microorganisms based on their motility and fermentation reactions. Fermentation of carbohydrate changes the medium yellow.
Trypticase Novobiocin Broth (TN Broth) Composition per liter: Pancreatic digest of casein................................17.0g NaCl....................................................................5.0g Papaic digest of soybean meal............................3.0g K2HPO4...............................................................2.5g Glucose ...............................................................2.5g Bile salts no. 3.....................................................1.5g K2HPO4...............................................................1.5g Novobiocin solution...................................... 10.0mL pH 7.3 ± 0.2 at 25°C
Novobiocin Solution: Composition per 10.0mL: Novobiocin .......................................................0.02g
Composition per liter:
Preparation of Novobiocin Solution: Add no-
Pancreatic digest of casein................................20.0g Agar ....................................................................3.5g Phenol Red........................................................0.02g pH 7.4 ± 0.2 at 25°C
vobiocin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Source: This medium is available as a premixed powder from BD Diagnostic Systems and Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the differentiation of microorganisms based on their motility.
Trypticase Agar Base with Carbohydrate Composition per liter: Pancreatic digest of casein................................20.0g Carbohydrate.......................................................5.0g Agar ....................................................................3.5g Phenol Red........................................................0.02g pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes. Autoclave for 15 min at 13 psi pressure–118°C. Do not overheat. Pour into sterile Petri dishes or leave in tubes.
Preparation of Medium: Add components, except novobiocin solution, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile novobiocin solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation of verotoxin-producing Escherichia coli.
Trypticase Peptone Glucose Yeast Extract Broth (TPGY Broth) Composition per liter: Pancreatic digest of casein................................50.0g Yeast extract......................................................20.0g Peptone ...............................................................5.0g Glucose ...............................................................4.0g Sodium thioglycolate ..........................................1.0g pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes in 15.0mL volumes. Autoclave for 10 min at 15 psi pressure– 121°C.
Use: For the cultivation of Clostridium botulinum.
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Trypticase Peptone Glucose Yeast Extract Broth, Buffered
Trypticase Peptone Glucose Yeast Extract Broth, Buffered Composition per liter: Pancreatic digest of casein................................50.0g Yeast extract......................................................20.0g Na2HPO4 .............................................................5.0g Peptone................................................................5.0g Glucose ...............................................................4.0g Sodium thioglycolate ..........................................1.0g pH 7.3 ± 0.2 at 25°C
Preparation of Medium: Add components to
Agar ..................................................................15.0g Papaic digest of soybean meal............................5.0g NaCl....................................................................5.0g pH 7.3 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Do not overheat. Pour into sterile Petri dishes or leave in tubes.
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat until dissolved. Adjust pH to 7.3. Distribute into tubes in 15.0mL volumes. Autoclave for 8 min at 15 psi pressure–121°C.
Use: For the isolation and cultivation of a wide variety
Use: For the isolation and cultivation of Clostridium perfringens.
Trypticase Soy Agar with Human Blood
Trypticase Peptone Glucose Yeast Extract Broth with Trypsin (TPGYT Broth) Composition per 1067.0mL: Pancreatic digest of casein................................50.0g Yeast extract......................................................20.0g Peptone................................................................5.0g Glucose ...............................................................4.0g Sodium thioglycolate ..........................................1.0g Trypsin solution ............................................ 67.0mL pH 7.0 ± 0.2 at 25°C
Trypsin Solution: Composition per 100.0mL: Trypsin ................................................................1.5g
Preparation of Trypsin Solution: Add trypsin to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except trypsin solution, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes in 15.0mL volumes. Autoclave for 10 min at 15 psi pressure– 121°C. Immediately prior to use, aseptically add 1.0mL of sterile trypsin solution to each tube. Mix thoroughly.
Use: For the cultivation of Clostridium botulinum.
Trypticase Soy Agar (Tryptic Soy Agar) (Soybean Casein Digest Agar) (ATCC Medium 77) Composition per liter: Pancreatic digest of casein................................15.0g
of fastidious as well as nonfastidious microorganisms.
Composition per liter: Pancreatic digest of casein................................15.0g Agar ..................................................................15.0g Papaic digest of soybean meal............................5.0g NaCl....................................................................5.0g Human blood, defibrinated ........................... 50.0mL pH 7.3 ± 0.2 at 25°C
Preparation of Medium: Add components, except human blood, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile human blood. Mix thoroughly. Pour into sterile Petri dishes in 17.0mL volumes or distribute into sterile tubes.
Use: For the cultivation of a wide variety of fastidious microorganisms. For the observation of hemolytic reactions of a variety of bacteria. May be used to perform the CAMP test for the presumptive identification of group B streptococci (Streptococcus agalactiae).
Trypticase Soy Agar with Lecithin and Polysorbate 80 (Microbial Content Test Agar) Composition per liter: Pancreatic digest of casein................................15.0g Agar ..................................................................15.0g Papaic digest of soybean meal............................5.0g NaCl....................................................................5.0g Polysorbate 80 (Tween 80) .................................5.0g Lecithin ...............................................................0.7g pH 7.3 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Trypticase Soy Agar with Sheep Blood, Formate, and Fumarate Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 13 psi pressure–118°C. Cool to 45°–50°C. Pour into sterile Petri dishes in 17.0mL volumes or leave in tubes.
Use: For the detection and enumeration of microorganisms in replicate plating techniques. Also used for the detection and enumeration of microorganisms present on surfaces of sanitary importance.
Trypticase Soy Agar, Modified (ATCC Medium 1481) Composition per liter: Pancreatic digest of casein................................17.0g Agar ..................................................................15.0g NaCl ....................................................................5.0g Papaic digest of soybean meal ............................3.0g K2HPO4 ...............................................................2.5g Glucose ...............................................................2.5g L-Glutamine................................................... 10.0mL pH 6.5 ± 0.2 at 25°C
Preparation of Medium: Add components, except glutamine, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 10.0mL of sterile glutamine. Mix thoroughly. Adjust pH to 6.5. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: Used as a base that is supplemented. For the cultivation of fastidious microorganisms. When supplemented with sheep blood, this medium is useful for the observation of hemolytic reactions of a variety of bacteria.
Trypticase Soy Agar, Modified (TSA II™) Composition per liter: Pancreatic digest of casein................................14.5g Agar ..................................................................14.0g Papaic digest of soybean meal ............................5.0g NaCl ....................................................................5.0g Growth factors (BD Diagnostic Systems) ..........1.5g pH 7.3 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Distribute into tubes or flasks. Autoclave
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for 15 min at 15 psi pressure–121°C. Do not overheat. Pour into sterile Petri dishes or leave in tubes. For blood plates, 50.0–100.0mL of sterile defibrinated sheep blood may be added to sterile medium that has been melted and cooled to 45°–50°C.
Use: Used as a base that is supplemented. For the cultivation of fastidious microorganisms. When supplemented with sheep blood, this medium is useful for the observation of hemolytic reactions of a variety of bacteria. It may be used to perform the CAMP test for the presumptive identification of group B streptococci (Streptococcus agalactiae).
Trypticase Soy Agar with Sheep Blood (Tryptic Soy Blood Agar) (TSA Blood Agar) Composition per liter: Pancreatic digest of casein................................15.0g Agar ..................................................................15.0g Papaic digest of soybean meal............................5.0g NaCl....................................................................5.0g Sheep blood, defibrinated ............................. 50.0mL pH 7.3 ± 0.2 at 25°C
Preparation of Medium: Add components, except sheep blood, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile sheep blood. Mix thoroughly. Pour into sterile Petri dishes in 17.0mL volumes or distribute into sterile tubes.
Use: For the cultivation of a wide variety of fastidious microorganisms. For the observation of hemolytic reactions of a variety of bacteria. May be used to perform the CAMP test for the presumptive identification of group B streptococci (Streptococcus agalactiae).
Trypticase Soy Agar with Sheep Blood, Formate, and Fumarate Composition per liter: Pancreatic digest of casein................................14.5g Agar ..................................................................14.0g Papaic digest of soybean meal............................5.0g NaCl....................................................................5.0g Sucrose................................................................2.0g Growth factors ....................................................1.5g Sheep blood, defibrinated ............................. 50.0mL Formate-fumarate solution............................ 13.0mL pH 7.3 ± 0.2 at 25°C
Source: Growth factors are available as a premixed powder from BD Diagnostic Systems.
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Trypticase Soy Agar with Sheep Blood and Gentamicin
Formate-Fumarate Solution: Composition per 100.0mL: Sodium formate...................................................6.0g Fumaric acid .......................................................6.0g
Preparation of Formate-Fumarate Solution: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Adjust pH to 7.0. Filter sterilize.
Preparation of Medium: Add components, except sheep blood, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile sheep blood. Mix thoroughly. Pour into sterile Petri dishes. Prior to inoculation, aseptically spread 0.2mL of sterile formate-fumarate solution on each plate.
Use: For the isolation of Streptococcus pneumoniae from a variety of clinical specimens.
Trypticase Soy Agar with Sheep Blood and Gentamicin (TSA II with Sheep Blood and Gentamicin) Composition per liter: Pancreatic digest of casein................................14.5g Agar ..................................................................14.0g Papaic digest of soybean meal ............................5.0g NaCl ....................................................................5.0g Growth factors ....................................................1.5g Sheep blood, defibrinated ............................. 50.0mL Gentamicin solution...................................... 10.0mL pH 7.3 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Gentamicin Solution: Composition per 10.0mL: Gentamicin.......................................................2.5mg
Preparation of Gentamicin Solution: Add gentamicin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except sheep blood and gentamicin solution, to distilled/deionized water and bring volume to 940.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C. Aseptically add sterile sheep blood and sterile gentamicin solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation of Streptococcus pneumoniae from a variety of clinical specimens.
Trypticase Soy Agar with Sheep Blood, Sucrose, and Tetracycline Composition per liter: Pancreatic digest of casein................................14.5g Agar ..................................................................14.0g Papaic digest of soybean meal............................5.0g NaCl....................................................................5.0g Sucrose................................................................2.0g Growth factors ....................................................1.5g Sheep blood, defibrinated ............................. 50.0mL Tetracycline solution..................................... 10.0mL pH 7.3 ± 0.2 at 25°C
Source: Growth factors are available as a premixed powder from BD Diagnostic Systems.
Tetracycline Solution: Composition per 10.0mL: Tetracycline......................................................0.5mg
Preparation of Tetracycline Solution: Add tetracycline to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except sheep blood and tetracycline solution, to distilled/deionized water and bring volume to 940.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile sheep blood and sterile tetracycline solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation of Streptococcus pneumoniae from a variety of clinical specimens.
Trypticase Soy Agar with Tobramycin Composition per liter: Pancreatic digest of casein................................17.0g Agar ..................................................................15.0g NaCl....................................................................5.0g Papaic digest of soybean meal............................3.0g K2HPO4...............................................................2.5g Glucose ...............................................................2.5g Tobramycin solution ..................................... 10.0mL pH 7.3 ± 0.2 at 25°C
Tobromycin Solution: Composition per 10.0mL: Tobramycin ......................................................8.0mg
Preparation of Tobromycin Solution: Add tobramycin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except tobramycin solution, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi
Trypticase Soy Broth with 10 mM Glucose pressure–121°C. Cool to 45°–50°C. Aseptically add sterile tobramycin solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation and maintenance of Serratia marcescens.
Trypticase Soy Agar with Sheep Blood and Tween 80 (ATCC Medium 1893) Composition per liter: Pancreatic digest of casein................................15.0g Agar ..................................................................15.0g Papaic digest of soybean meal ............................5.0g NaCl ....................................................................5.0g Sheep blood, defibrinated ............................. 50.0mL Tween 80....................................................... 10.0mL pH 7.3 ± 0.2 at 25°C
Preparation of Medium: Add components, except sheep blood, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile sheep blood. Mix thoroughly. Pour into sterile Petri dishes in 17.0mL volumes or distribute into sterile tubes.
Use: For the cultivation of a wide variety of fastidious microorganisms.
Trypticase Soy Agar with Sheep Blood and Vacnomycin (ATCC Medium 1976) Composition per liter: Pancreatic digest of casein................................14.5g Agar ..................................................................14.0g Papaic digest of soybean meal ............................5.0g NaCl ....................................................................5.0g Growth factors ....................................................1.5g Sheep blood, defibrinated ............................. 50.0mL Vancomycin solution..................................... 10.0mL pH 7.3 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Vancomycin Solution: Composition per 10.0mL:
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940.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 50°–55°C. Aseptically add sterile sheep blood and sterile gentamicin solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation of Streptococcus and Enterococcus spp. from a variety of clinical specimens.
Trypticase Soy Agar Yeast Extract (TSAYE) Composition per liter: Pancreatic digest of casein................................17.0g Agar ..................................................................15.0g Yeast extract........................................................6.0g NaCl....................................................................5.0g Papaic digest of soybean meal............................3.0g K2HPO4...............................................................2.5g Glucose ...............................................................2.5g pH 7.3 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of a wide variety of heterotrophic microorganisms. For the isolation and cultivation of Listeria monocytogenes.
Trypticase Soy Broth with 10mM Glucose Composition per liter: Pancreatic digest of casein................................17.0g NaCl....................................................................5.0g Papaic digest of soybean meal............................3.0g K2HPO4...............................................................2.5g Glucose ...............................................................1.8g pH 7.3 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of a variety of fastidious and
Vacnomycin .....................................................4.0mg
nonfastidious microorganisms from clinical and nonclinical specimens.
Preparation of Vancomycin Solution: Add vancomycin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Trypticase Soy Broth with 10 mM Glucose
Preparation of Medium: Add components, except sheep blood and vancomycin solution, to distilled/deionized water and bring volume to
(ATCC Medium 1189) Composition per liter: Pancreatic digest of casein................................18.0g
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Trypticase Soy Broth without Glucose
Papaic digest of soybean meal ............................6.0g NaCl ....................................................................6.0g Glucose ...............................................................1.0g pH 7.3 ± 0.2 at 25°C
Source: This medium without glucose is available as a premixed powder from BD Diagnostic Systems.
NaCl....................................................................5.0g Papaic digest of soybean meal............................3.0g K2HPO4...............................................................2.5g Glucose ...............................................................2.5g Sheep blood, defibrinated ............................. 50.0mL
Preparation of Medium: Add components, ex-
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Do not overheat. Pour into sterile Petri dishes or leave in tubes.
cept sheep blood, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 50.0mL of sterile, defibrinated sheep blood. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the isolation and cultivation of Staphylococ-
Use: For cultivation and maintenance of Bartonella
Preparation of Medium: Add components to
cus aureus subsp. aureus
bacilliformis.
Trypticase Soy Broth with Tobramycin
Trypticase Soy Broth without Glucose Composition per liter: Pancreatic digest of casein................................17.0g NaCl ....................................................................5.0g Papaic digest of soybean meal ............................3.0g K2HPO4 ...............................................................2.5g pH 7.3 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of a wide variety of micro-
Composition per liter: Pancreatic digest of casein................................17.0g NaCl....................................................................5.0g Papaic digest of soybean meal............................3.0g K2HPO4...............................................................2.5g Glucose ...............................................................2.5g Agar ....................................................................1.0g Tobramycin solution ..................................... 10.0mL pH 7.3 ± 0.2 at 25°C
Tobromycin Solution: Composition per 10.0mL: Tobramycin ......................................................8.0mg
organisms when the presence of carbohydrate is undesirable.
Preparation of Tobromycin Solution: Add to-
Trypticase Soy Broth with 1.5% NaCl
Preparation of Medium: Add components, ex-
Composition per liter: Pancreatic digest of casein................................17.0g NaCl ..................................................................15.0g Papaic digest of soybean meal ............................3.0g K2HPO4 ...............................................................2.5g Glucose ...............................................................2.5g pH 7.3 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation and maintenance of Pasteurella species.
Trypticase Soy Broth with Sheep Blood (LMG Medium 189) Composition per liter: Pancreatic digest of casein................................17.0g
bramycin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. cept tobramycin solution, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile tobramycin solution. Mix thoroughly. Aseptically distribute into sterile tubes.
Use: For the cultivation and maintenance of Serratia marcescens.
Trypticase Soy Broth with Tween 80 Composition per liter: Pancreatic digest of casein................................17.0g NaCl....................................................................5.0g Papaic digest of soybean meal............................3.0g K2HPO4...............................................................2.5g Glucose ...............................................................2.5g Agar ....................................................................1.0g Tween 80......................................................... 1.0mL pH 7.3 ± 0.2 at 25°C
Tryptone Bile X-glucuronide Agar, Chromocult Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation and maintenance of Coryne-
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serum, or human serum may be used. Mix thoroughly. Pour into sterile Petri dishes.
Use: For the selective isolation of microorganisms from clinical specimens, especially from the nose, throat, and vagina.
bacterium genitalium.
Trypticase Soy Broth with Yeast Extract Composition per liter: Pancreatic digest of casein................................17.0g Yeast extract........................................................6.0g NaCl ....................................................................5.0g Papaic digest of soybean meal ............................3.0g K2HPO4 ...............................................................2.5g Glucose ...............................................................2.5g pH 7.3 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation and maintenance of a wide variety of heterotrophic microorganisms.
Trypticase Tellurite Agar Base Composition per liter: Agar ..................................................................20.0g Pancreatic digest of casein................................10.0g Peptic digest of animal tissue............................10.0g NaCl ....................................................................5.0g Glucose ...............................................................2.0g Serum ............................................................ 50.0mL Chapman tellurite solution............................ 10.0mL pH 7.5 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Chapman Tellurite Solution: Composition per 100.0mL:
Tryptone Bile Glucuronide Agar, Harlequim (Harlequin TBGA) Composition per liter: Tryptone............................................................20.0g Agar ..................................................................15.0g Bilie salts no. 3 ...................................................1.5g X-glucuronide .................................................0.075g pH 7.2 ± 0.2 at 25°C
Source: This medium is available from lab m. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Allow to soak for 10 min. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°– 50°C. Pour into sterile Petri dishes.
Use: For the simple enumeration of E. coli without the need for membranes, or preincubation. The medium has been modified by the addition of a chromogenic substrate to detect the β-glucuronidase, which is highly specific for E. coli. The advantage of the chromogenic substrate is that it requires no UV lamp to visualise the reaction, and it is concentrated within the colony, facilitating easier enumeration in the presence of other organisms, or when large numbers are present on the plate.
Tryptone Bile X-glucuronide Agar, Chromocult (Chromocult TBX ) (ChromocultTryptone Bile X-glucuronide Agar) Composition per liter:
Add K2TeO3 to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Peptone ............................................................20.0g Agar ..................................................................15.0g Bile salts no. 3 ....................................................1.5g X-β-D-glucuronide .........................................0.075g pH 7.2 ± 0.2 at 25°C
Caution: Potassium tellurite is toxic.
Source: This medium is available from Merck.
Preparation of Medium: Add components, ex-
Preparation of Medium: Add components to
K2TeO3 ................................................................1.0g
Preparation of Chapman Tellurite Solution:
cept serum and Chapman tellurite solution, to distilled/deionized water and bring volume to 940.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile serum and sterile Chapman tellurite solution. Sheep serum, rabbit
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Pour into sterile Petri dishes.
Use: For the differentiation of E. coli from other coliforms. The presence of the enzyme β-D-glucu-
452
Tryptone Phosphate Broth
ronidase differentiates most E. coli spp. from other coliforms. E. coli absorbs the chromogenic substrate 5-bromo-4-chloro-3-indolyl-β-D-glucuronide (X-β-Dglucuronide). The enzyme β-glucuronidase splits the bond between the chromophore 5-bromo-4-chloro-3indolyle- and the β-D-glucuronide. E. coli colonies are colored blue-green. Growth of accompanying Grampositive flora is largely inhibited by the use of bile salts The prepared medium is clear and yellowish.
Source: This medium is available as a premixed
Tryptone Phosphate Broth
Tryptone Soya Broth with 0.1% Tween 80
Composition per liter:
powder from Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of a wide variety of microorganisms.
Pancreatic digest of casein................................20.0g NaCl ....................................................................5.0g K2HPO4 ..............................................................2.0g KH2PO4 ..............................................................2.0g Tween 80....................................................... 15.0mL pH 7.0 ± 0.2 at 25°C
Composition per liter:
Preparation of Medium: Add components to
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of enteropathogenic Escher-
Pancreatic digest of casein................................15.0g Papaic digest of soybean meal............................5.0g NaCl....................................................................5.0g Tween 80.............................................................1.0g
Preparation of Medium: Add components to
Use: For the cultivation of Corynebacterium genitalium and Corynebacterium pseudogenitalium.
ichia coli.
Tryptone Soya Agar Composition per liter: Agar ..................................................................15.0g Pancreatic digest of casein................................15.0g NaCl ....................................................................5.0g Pancreatic digest of soybean meal ......................5.0g pH 7.3 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of a wide variety of microorganisms.
Tryptone Soya Broth Composition per liter: Pancreatic digest of casein................................17.0g NaCl ....................................................................5.0g Pancreatic digest of soybean meal ......................3.0g K2HPO4 ...............................................................2.5g Glucose ...............................................................2.5g pH 7.3 ± 0.2 at 25°C
Tryptone Water Broth (Tryptone Broth) Composition per liter: Pancreatic digest of casein................................10.0g NaCl....................................................................5.0g pH 7.5 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of production of indole by microorganisms.
Tryptone Yeast Extract Agar Composition per liter: Pancreatic digest of casein................................10.0g Agar ....................................................................2.0g Yeast extract........................................................1.0g Bromcresol Purple ............................................0.04g Carbohydrate solution................................. 100.0mL pH 7.0 ± 0.2 at 25°C
Carbohydrate Solution: Composition per 100.0mL: Carbohydrate.....................................................10.0g
Tryptose Agar with Sheep Blood Preparation of Carbohydrate Solution: Add carbohydrate to distilled/deionized water and bring volume to 100.0mL. Glucose or mannitol may be used. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except carbohydrate solution, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Adjust pH to 7.0. Gently heat and bring to boiling. Distribute into tubes in 13.5mL volumes. Autoclave for 20 min at 10 psi pressure–115°C. Cool to 45°– 50°C. Aseptically add 1.5mL of carbohydrate solution to each tube. Mix thoroughly. Solidify agar quickly by placing tubes in ice water.
Use: For the cultivation and differentiation of Staphylococcus aureus based on glucose and mannitol fermentation. Bacteria that ferment the added carbohydrate turn the medium yellow.
Tryptone Yeast Extract Agar 1 Composition per liter: Agar ..................................................................20.0g Pancreatic digest of casein................................10.0g Yeast extract........................................................5.0g K2HPO4 ..............................................................4.4g Glucose ...............................................................2.0g NaCl ....................................................................2.0g pH 7.2 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.2. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
453
Tryptose Agar Composition per liter: Agar ..................................................................15.0g Pancreatic digest of casein................................10.0g Peptic digest of animal tissue ...........................10.0g NaCl....................................................................5.0g Glucose ...............................................................1.0g pH 7.2 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of fastidious aerobic and facultative microorganisms.
Tryptose Agar with Citrate Composition per liter: Agar ..................................................................15.0g Pancreatic digest of casein................................10.0g Peptic digest of animal tissue ...........................10.0g Sodium citrate...................................................10.0g NaCl....................................................................5.0g Glucose ...............................................................1.0g pH 7.2 ± 0.2 at 25°C
Preparation of Medium: Add components to
Use: For the cultivation and maintenance of a wide
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
variety of heterotrophic bacteria.
Use: For the cultivation and maintenance of fastidi-
Tryptophan 1% Solution (Trypticase 1% Solution) (Tryptone 1% Solution) Composition per liter: Pancreatic digest of casein................................10.0g pH 7.0 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the differentiation of bacteria, especially members of the Enterobacteaceae, based on their production of indole.
ous aerobic and facultative microorganisms, including Brucella species and streptococci.
Tryptose Agar with Sheep Blood (ATCC Medium 546) Composition per liter: Agar ..................................................................15.0g Tryptose ............................................................10.0g NaCl....................................................................5.0g Beef extract.........................................................3.0g Sheep blood, defibrinated ...................50.0-100.0mL pH 7.3 ± 0.2 at 25°C
Preparation of Medium: Add components, except sheep blood, to distilled/deionized water and bring volume to 900–950mL. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes. Autoclave for 15 min at 15 psi pressure–121°C. Cool
454
Tryptose Agar with Thiamine
to 45°–50°C. Aseptically add sterile sheep blood. Mix thoroughly. Pour into sterile Petri dishes in 17.0mL volumes or distribute into sterile tubes.
Use: For the cultivation and maintenance of a wide
Beef extract.........................................................3.0g Yeast extract........................................................1.0g Sheep blood, defibrinated ............................. 50.0mL pH 7.3 ± 0.2 at 25°C
variety of fastidious microorganisms.
Source: This medium is available as a premixed
Tryptose Agar with Thiamine Composition per liter: Agar ..................................................................15.0g Pancreatic digest of casein................................10.0g Peptic digest of animal tissue............................10.0g NaCl ....................................................................5.0g Glucose ...............................................................1.0g Thiamine·HCl ..................................................5.0mg pH 7.2 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of fastidious aerobic and facultative microorganisms, including Brucella species and streptococci.
Tryptose Blood Agar Composition per liter: Agar ..................................................................12.0g Tryptose ............................................................10.0g NaCl ....................................................................5.0g Beef extract .........................................................3.0g Sheep blood, defibrinated ............................. 70.0mL pH 7.2 ± 0.2 at 25°C
Source: This medium is available as a premixed
powder from BD Diagnostic Systems.
Preparation of Medium: Add components, except sheep blood, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile sheep blood. Mix thoroughly. Pour into sterile Petri dishes in 17.0mL volumes or distribute into sterile tubes.
Use: For the cultivation and maintenance of a wide variety of fastidious microorganisms.
Tryptose Broth Composition per liter: Pancreatic digest of casein................................10.0g Peptic digest of animal tissue ...........................10.0g NaCl....................................................................5.0g Glucose ...............................................................1.0g pH 7.2 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of fastidious aerobic and facultative microorganisms, including streptococci.
powder from Oxoid Unipath.
Preparation of Medium: Add components, except sheep blood, to distilled/deionized water and bring volume to 930.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile sheep blood. Mix thoroughly. Pour into sterile Petri dishes in 17.0mL volumes or distribute into sterile tubes.
Use: For the cultivation and maintenance of a wide variety of fastidious microorganisms.
Tryptose Blood Agar Base with Yeast Extract Composition per liter: Agar ..................................................................15.0g Tryptose ............................................................10.0g NaCl ....................................................................5.0g
Tryptose Broth Composition per liter: Pancreatic digest of casein................................10.0g Peptic digest of animal tissue ...........................10.0g NaCl....................................................................5.0g Glucose ...............................................................1.0g Thiamine·HCl ..................................................5.0mg pH 7.2 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of fastidious aerobic and facultative microorganisms.
Tryptose Phosphate Broth, Modified
Preparation of Medium: Add components to
Tryptose Broth with Citrate Composition per liter: Pancreatic digest of casein................................10.0g Peptic digest of animal tissue............................10.0g Sodium citrate ...................................................10.0g NaCl ....................................................................5.0g Glucose ...............................................................1.0g Thiamine·HCl ..................................................5.0mg pH 7.2 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the isolation and cultivation of a variety of fastidious aerobic microorganisms, especially Brucella species, from clinical sources.
Tryptose Cycloserine Dextrose Agar
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of Erysipelothris tonsillarum.
Tryptose Phosphate Broth Composition per liter: Tryptose ............................................................20.0g NaCl....................................................................5.0g Na2HPO4 .............................................................2.5g Glucose ...............................................................2.0g pH 7.3 ± 0.2 at 25°C
Source: This medium is available as a premixed
Composition per liter: Agar ..................................................................20.0g Tryptose ............................................................15.0g Pancreatic digest of soybean meal ......................5.0g Yeast extract........................................................5.0g Ferric ammonium citrate.....................................1.0g Cycloserine solution ..................................... 10.0mL pH 7.6 ± 0.2 at 25°C
Cycloserine Solution: Composition per 10.0mL: D-Cycloserine ......................................................0.4g
Preparation of Cycloserine Solution: Add
455
powder from BD Diagnostic Systems and Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Prior to the inoculation of anaerobic microorganisms, place tubes of sterile medium in a 100°C bath for 15 min and cool undisturbed.
Use: For the cultivation of a variety of fastidious bacteria.
D-
cycloserine to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except cycloserine solution, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile cycloserine solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation and cultivation of Clostridium species, especially Clostridium botulinum.
Tryptose Phosphate Agar Composition per liter: Tryptose ............................................................20.0g Agar ..................................................................15.0g NaCl ....................................................................5.0g Na2HPO4 .............................................................2.5g Glucose ...............................................................2.0g pH 7.3 ± 0.2 at 25°C
Tryptose Phosphate Broth, Modified Composition per liter: Enzymatic digest of casein ...............................20.0g NaCl....................................................................5.0g Na2HPO4 .............................................................2.5g Glucose ...............................................................2.0g pH 7.3 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Prior to the inoculation of anaerobic microorganisms, place tubes of sterile medium in a 100°C bath for 15 min and cool undisturbed.
Use: For the cultivation of a variety of fastidious microorganisms, including pneumococci, streptococci, and meningococci.
456
Tryptose Sulfite Cycloserine Agar
Tryptose Sulfite Cycloserine Agar (TSC Agar) Composition per liter: Tryptose ............................................................15.0g Agar ..................................................................14.0g Pancreatic digest of soybean meal ......................5.0g Yeast extract........................................................5.0g Ferric ammonium citrate.....................................1.0g Na2S2O5 ..............................................................1.0g Cycloserine solution ..................................... 10.0mL pH 7.6 ± 0.2 at 25°C
Cycloserine Solution: Composition per 10.0mL: D-Cycloserine ......................................................0.4g
Preparation of Cycloserine Solution: Add cycloserine to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except cycloserine solution, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile cycloserine solution. Mix thoroughly. Pour into sterile Petri dishes.
Use: For the presumptive identification and enumeration of Clostridium perfringens.
Tryptose Sulfite Cycloserine Agar (TSC Agar) Composition per liter: Tryptose ............................................................15.0g Agar ..................................................................14.0g Beef extract .........................................................5.0g Pancreatic digest of soybean meal ......................5.0g Yeast extract........................................................5.0g Ferric ammonium citrate.....................................1.0g Na2S2O5 ..............................................................1.0g Egg yolk emulsion ........................................ 50.0mL Cycloserine solution ..................................... 10.0mL pH 7.6 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath. Egg Yolk Emulsion: Composition: Chicken egg yolks..................................................11 Whole chicken egg...................................................1
Preparation of Egg Yolk Emulsion: Soak eggs with 1:100 dilution of saturated mercuric chloride solution for 1 min. Crack eggs and separate yolks from whites. Mix egg yolks with 1 chicken egg.
Cycloserine Solution: Composition per 10.0mL: D-Cycloserine ......................................................0.4g
Preparation of Cycloserine Solution: Add cycloserine to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except cycloserine solution and egg yolk emulsion, to distilled/deionized water and bring volume to 940.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C. Aseptically add sterile cycloserine solution and egg yolk emulsion. Mix thoroughly. Pour into sterile Petri dishes.
Use: For the presumptive identification and enumeration of Clostridium perfringens.
Tryptose Sulfite Cycloserine Agar with Polymyxin and Kanamycin Composition per liter: Tryptose ............................................................15.0g Agar ..................................................................14.0g Beef extract.........................................................5.0g Pancreatic digest of soybean meal......................5.0g Yeast extract........................................................5.0g Ferric ammonium citrate.....................................1.0g Na2S2O5 ..............................................................1.0g Antibiotic solution ........................................ 10.0mL pH 7.6 ± 0.2 at 25°C
Antibiotic Solution: Composition per 10.0mL: D-Cycloserine ......................................................0.4g
Polymyxin B sulfate .........................................0.03g Kanamycin sulfate ..........................................0.012g
Preparation of Antibiotic Solution: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except antibiotic solution, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile antibiotic solution. Mix thoroughly. Pour into sterile Petri dishes.
Use: For the isolation and enumeration of Clostridium perfringens from clinical specimens.
Tryptose Sulfite Cycloserine Agar without Egg Yolk (TSC Agar without Egg Yolk) Composition per liter: Tryptose ............................................................15.0g
TSN Agar Agar ..................................................................14.0g Beef extract .........................................................5.0g Pancreatic digest of soybean meal ......................5.0g Yeast extract........................................................5.0g Ferric ammonium citrate.....................................1.0g Na2S2O5 ..............................................................1.0g Cycloserine solution ..................................... 10.0mL pH 7.6 ± 0.2 at 25°C
Cycloserine Solution: Composition per 10.0mL: D-Cycloserine ......................................................0.4g
457
fluorogenic substrate for the alkaline and acid phosphatase. The acid phosphatase is a highly specific indicator for C. perfringens. The acid phosphatase splits the fluorogenic substrate MUP forming 4-methylumbelliferone which can be identified as it fluorescence in long wave UV light. Thus a strong suggestion for the presence of C. perfringens can be obtained. The acid phosphatase splits the fluorogenic substrate MUP forming 4-methylumbelliferone which can be identified as it fluorescence in long wave UV light, providing a strong suggestion for the presence of Clostridium perfringens.
Preparation of Cycloserine Solution: Add cycloserine to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except cycloserine solution, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile cycloserine solution. Mix thoroughly. Pour into sterile Petri dishes.
Use: For the presumptive identification and enumeration of Clostridium perfringens.
TSC Agar, Fluorocult (Fluorocult TSC Agar) (Fluorocult Tryptose Sulfite Cycloserine Agar) (Tryptose Sulfite Cycloserine Agar, Fluorocult) Composition per liter: Agar ..................................................................15.0g Tryptose ............................................................15.0g Peptone from soymeal ........................................5.0g Yeast extract........................................................5.0g Na2S2O5 ..............................................................1.0g Ammonium ferric citrate ....................................1.0g D-Cycloserine......................................................0.2g 4-Methylumbelliferyl-phosphate disodium salt............................................50.0mg
Source: This medium is available from Merck. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Pour into sterile Petri dishes.
TSN Agar (Trypticase Sulfite Neomycin Agar) Composition per liter: Pancreatic digest of casein................................15.0g Agar ..................................................................13.5g Yeast extract......................................................10.0g Na2SO3 ................................................................1.0g Ferric citrate........................................................0.5g Neomycin sulfate ..............................................0.05g Polymyxin sulfate .............................................0.02g Buffered thioglycolate solution .................... 50.0mL pH 7.2 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Buffered Thioglycolate Solution: Composition per 50.0mL: Buffer solution .............................................. 35.0mL Sodium thioglycolate solution ...................... 15.0mL
Preparation of Buffered Thioglycolate Solution: Combine components. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Buffer Solution: Composition per 100.0mL: Na2CO3 .............................................................28.0g K2HPO4...............................................................5.7g
Preparation of Buffer Solution: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly.
Thioglycolate Solution: Composition per 100.0mL: Sodium thioglycolate ........................................13.3g
Preparation of Thioglycolate Solution: Add
Use: For the isolation and enumeration of the vege-
sodium thioglycolate to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly.
tative and spore forms of Clostridium perfringens. DCycloserine inhibits the accompanying bacterial flora and causes the colonies which develop to remain smaller. 4-Methylumbelliferyl-phosphate (MUP) is a
cept buffered thioglycolate solution, to distilled/ deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Auto-
Preparation of Medium: Add components, ex-
458
Tween 80 Hydrolysis Broth
clave for 12 min at 13 psi pressure–118°C. Do not overheat. Cool to 45°–50°C. Aseptically add buffered thioglycolate solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the selective isolation of Clostridium perfringens.
Tween 80 Hydrolysis Broth Composition per liter:
Tween 80 Solution: Composition per 50.0mL: Tween 80...........................................................10.0g
Preparation of Tween 80 Solution: Add Tween 80 to distilled/deionized water and bring volume to 50.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Preparation of Medium: Add components, ex-
Na2HPO4 ...........................................................5.79g NaH2PO4 ...........................................................3.53g Neutral Red .......................................................0.02g Tween 80 solution ........................................... 5.0mL pH 7.0 ± 0.2 at 25°C
cept Tween 80 solution, to distilled/deionized water and bring volume to 975.0mL. Mix thoroughly. Adjust pH to 7.2. Autoclave for 15 min at 15 psi pressure–121°C. Aseptically add 25.0mL of sterile Tween 80 solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Tween 80 Solution: Composition per 50.0mL:
Use: For the differentiation of Mycobacterium spe-
Tween 80...........................................................10.0g
Preparation of Tween 80 Solution: Add Tween 80 to distilled/deionized water and bring volume to 50.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Preparation of Medium: Add components, except Tween 80 solution, to distilled/deionized water and bring volume to 995.0mL. Mix thoroughly. Adjust pH to 7.2. Autoclave for 15 min at 15 psi pressure–121°C. Aseptically add 5.0mL of sterile Tween 80 solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the differentiation of Mycobacterium species. Strains that hydrolyze Tween 80 within 5 days turn the medium pink to red.
Tween 80 Hydrolysis Broth Composition per 125.0mL: Neutral Red .........................................................0.1g Solution 1...................................................... 38.9mL Solution 2...................................................... 61.1mL Tween 80 solution ......................................... 25.0mL pH 7.0 ± 0.2 at 25°C
cies. Strains that hydrolyze Tween 80 within 5 days turn the medium pink to red.
Tween 80 Hydrolysis Broth Composition per 102.5mL: NaHPO4 (0.066M solution) .......................... 61.1mL KH2PO4 (0.066M solution)........................... 38.9mL Neutral Red (0.1% solution) ........................... 2.0mL Tween 80......................................................... 0.5mL pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Combine components. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the differentiation of Mycobacterium species. Strains that hydrolyze Tween 80 within 5 days turn the medium pink to red.
Tween 80 Hydrolysis Medium Composition per liter:
KH2PO4 .............................................................22.7g
Agar ..................................................................12.0g Peptone .............................................................10.0g Tween 80...........................................................10.0g NaCl....................................................................5.0g CaCl2 ...................................................................0.1g pH 7.2–7.4 at 25°C
Preparation of Solution 1: Add KH2PO4 to dis-
Preparation of Medium: Add components to dis-
Solution 2: Composition per 400.0mL:
tilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes.
Na2HPO4 ...........................................................23.8g
Use: For the cultivation and differentiation of
Preparation of Solution 2: Add Na2HPO4 to dis-
Pseudomonas species based on their ability to hydrolyze Tween 80. Bacteria that hydrolyze Tween 80 appear as colonies surrounded by an opaque zone.
Solution 1: Composition per 400.0mL:
tilled/deionized water and bring volume to 400.0mL. Mix thoroughly.
tilled/deionized water and bring volume to 400.0mL. Mix thoroughly.
TYI-S-33 Medium
TY Medium Composition per liter: Agar ..................................................................15.0g Pancreatic digest of casein..................................5.0g Yeast extract........................................................3.0g CaCl2·6H2O.........................................................1.3g
Preparation of Medium: Add components to
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distilled/deionized water and bring volume to 800.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C. Aseptically add the sterile CaCl2·2H2O solution and sterile glucose solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of a vari-
Use: For the cultivation of a wide variety of bacteria.
Pancreatic digest of casein............................... 20.0g Yeast extract......................................................10.0g NaCl....................................................................2.0g L-Cysteine·HCl ...................................................1.0g Ascorbic acid ..................................................... 0.2g Ferric ammonium citrate................................22.8mg Bovine serum, heat inactivated................... 100.0mL Special 107 vitamin mix ............................. 100.0mL Buffer solution .............................................. 50.0mL Glucose solution ........................................... 50.0mL pH 6.8 ± 0.2 at 25°C
TY Salt Medium Composition per liter: NaCl ..................................................................10.0g Pancreatic digest of casein................................10.0g Yeast extract........................................................5.0g pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of a wide variety of bacteria.
TYGS Medium (Tryptone Yeast Extract Glucose Salt Medium) Composition per liter: Agar ..................................................................15.0g Pancreatic digest of casein................................10.0g NaCl ....................................................................8.0g Yeast extract........................................................1.0g CaCl2·2H2O solution................................... 100.0mL Glucose solution ......................................... 100.0mL
CaCl2·2H2O Solution: Composition per 100.0mL: CaCl2·2H2O.........................................................0.3g
Preparation of CaCl2·2H2O Solution: Add the
CaCl2·2H2O to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Glucose Solution: Composition per 100.0mL:
ety of bacteria.
TYI-S-33 Medium Composition per liter:
Glucose Solution: Composition per 50.0mL: Glucose .............................................................10.0g
Preparation of Glucose Solution: Add glucose to distilled/deionized water and bring volume to 50.0mL. Mix thoroughly. Filter sterilize.
Buffer Solution: Composition per 50.0mL: K2HPO4...............................................................1.0g KH2PO4.............................................................. 0.6g
Preparation of Buffer Solution: Add components to distilled/deionized water and bring volume to 50.0mL. Mix thoroughly. Adjust pH to 6.8. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C.
Special 107 Vitamin Mix: Composition per 120.0.0mL: Solution 1........................................................ 1.2mL Solution 2........................................................ 0.4mL Solution 3........................................................ 0.4mL Solution 4 vitamins ..................................... 100.0mL
Preparation of Special 107 Vitamin Mix:
Preparation of Glucose Solution: Add glucose to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Aseptically combine 1.2mL of sterile solution 1, 0.4mL of sterile solution 2, 0.4mL of sterile solution 3, and 100.0mL of sterile solution 4 vitamins. Bring volume to 120.0mL with sterile distilled/deionized water.
Preparation of Medium: Add components, ex-
Solution 1:
cept CaCl2·2H2O solution and glucose solution, to
Vitamin B12 ....................................................40.0mg
D-Glucose ............................................................1.0g
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TYM Basal Medium, Modified 1
Preparation of Solution 1: Add vitamin B12 to
distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
TYM Basal Medium, Modified 1 Composition per liter:
DL-6,8-thioctic acid to absolute ethanol and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Pancreatic digest of peptone .............................20.0g Yeast extract......................................................10.0g Maltose ...............................................................5.0g L-Cysteine·HCl ...................................................1.0g K2HPO4...............................................................0.8g KH2PO4...............................................................0.8g Agar, noble..........................................................0.5g L-Ascorbic acid ...................................................0.2g pH 7.8 ± 0.2 at 25°C
Solution 3:
Preparation of Medium: Add components, except
Solution 2: Composition per 100.0.0mL: DL-6,8-Thioctic
acid, oxidized.....................100.0mg Absolute ethanol ......................................... 100.0mL
Preparation of Solution 2: Add
Tween 80...........................................................50.0g Absolute ethanol ......................................... 100.0mL
Preparation of Solution 3: Add Tween 80 to absolute ethanol and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Solution 4 Vitamins: Composition per liter: Vitamin B12 ....................................................10.0mg Calcium D-(+)-pantothenate.............................2.3mg Choline chloride.............................................1.25mg Riboflavin ........................................................0.7mg Calciferol (vitamin D2) ..................................0.25mg Vitamin A, crystallized alcohol .....................0.25mg p-Aminobenzoic acid...................................0.125mg i-Inositol.......................................................0.125mg Thiamine·HCl ..............................................0.025mg Niacin.........................................................0.0625mg Niacinamide ...............................................0.0625mg Pyridoxal·HCl ............................................0.0625mg Pyridoxine·HCl ..........................................0.0625mg Biotin ...........................................................0.025mg α-Tocopherol phosphate, disodium salt.......0.025mg Folic acid......................................................0.025mg Menadione (vitamin K3) ..............................0.025mg
agar, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.8 with NaOH. Add the agar. Mix thoroughly. Gently heat and bring to boiling. Distribute into screw-capped tubes. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation of Trichomonas species.
TYM Basal Medium, Modified 2 Composition per liter: Pancreatic digest of casein................................20.0g Yeast extract......................................................10.0g Maltose ...............................................................5.0g L-Cysteine·HCl ...................................................1.0g K2HPO4...............................................................0.8g KH2PO4...............................................................0.8g Agar, noble..........................................................0.5g L-Ascorbic acid ...................................................0.2g Lamb serum, heat inactivated ..................... 300.0mL pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Add components, ex-
ponents to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
cept agar and lamb serum, to distilled/deionized water and bring volume to 700.0mL. Mix thoroughly. Adjust to pH 7.0 with NaOH. Add the agar. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 25°C. Aseptically add 300.0mL of sterile, heat-inactivated lamb serum. Mix thoroughly. Aseptically distribute into sterile screw-capped tubes. Use soon after preparation.
Preparation of Medium: Add components, ex-
Use: For the cultivation of Trichomonas vaginalis
Preparation of Solution 4 Vitamins: Add com-
cept heat-inactivated bovine serum, special 107 vitamin solution, glucose solution, and buffer solution, to distilled/deionized water and bring volume to 700.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Aseptically add 100.0mL of sterile, heat-inactivated bovine serum, 100.0mL of sterile special 107 vitamin solution, 50.0mL of sterile glucose solution, and 50.0mL of sterile buffer solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation of Entamoeba species.
and Hypotrichomonas species.
TYM Basal Medium, Modified 4 Composition per liter: Pancreatic digest of casein................................20.0g Yeast extract......................................................10.0g Maltose ...............................................................5.0g L-Cysteine·HCl ...................................................1.0g K2HPO4...............................................................0.8g KH2PO4...............................................................0.8g Agar, noble..........................................................0.5g
U Broth L-Ascorbic
acid ...................................................0.2g Horse serum, heat inactivated..................... 300.0mL pH 6.0 ± 0.2 at 25°C
Preparation of Medium: Add components, except
Preparation of MES Buffer Solution: Add MES buffer to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Adjust pH to 5.5. Filter sterilize.
agar and horse serum, to distilled/deionized water and bring volume to 700.0mL. Mix thoroughly. Adjust pH to 6.0. Add the agar. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Aseptically add 300.0mL of heat-inactivated horse serum. Mix thoroughly. Aseptically distribute into screw-capped tubes.
Penicillin Solution: Composition per 10.0mL:
Use: For the cultivation of Tritrichomonas foetus
Urea Solution: Composition per 100.0mL:
and Trichomonas vaginalis.
U Agar Plates (Ureaplasma Agar Plates) (MES Agar) Composition per 100.2mL: Base agar....................................................... 65.0mL Horse serum .................................................. 20.0mL Yeast dialysate............................................... 10.0mL MES (2-N-Morpholinoethane sulfonic acid) buffer solution.................... 3.0mL Penicillin solution ........................................... 2.0mL Urea solution................................................... 0.2mL pH 5.5 ± 0.2 at 25°C
Base Agar: Composition per liter: Papaic digest of soybean meal ..........................20.0g Agarose .............................................................10.0g NaCl ....................................................................5.0g Phenol Red (2% solution) ............................... 1.0mL
Preparation of Base Agar: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Adjust pH to 7.3. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Yeast Dialysate: Composition per 10.0mL: Yeast, active dried ...........................................450.0g
Preparation of Yeast Dialysate: Add active, dried yeast to distilled/deionized water and bring volume to 1250.0mL. Gently heat and bring to 40°C. Autoclave for 15 min at 15 psi pressure–121°C. Put into dialysis tubing. Dialyze against 1.0L of distilled/ deionized water for 2 days at 4°C. Discard tubing and its contents. Autoclave dialysate for 15 min at 15 psi pressure–121°C. Store at −20°C. MES Buffer Solution: Composition per 100.0mL: MES (2-N-Morpholinoethane sulfonic acid) buffer .................................19.52g
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Penicillin .................................................... 100,000U
Preparation of Penicillin Solution: Add penicillin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Urea.....................................................................6.0g
Preparation of Urea Solution: Add urea to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: To 65.0mL of cooled, sterile base agar, aseptically add 10.0mL of sterile yeast dialysate, 20.0mL of horse serum, 2.0mL of sterile penicillin solution, 3.0mL of sterile MES buffer solution, and 0.2mL of sterile urea solution. Mix thoroughly. Pour into 10mm × 35mm Petri dishes in 5.0mL volumes. Allow plates to stand overnight at 25°C to remove excess surface moisture.
Use: For the isolation and cultivation of Ureaplasma species.
U Broth (Ureaplasma Broth) Composition per 99.5mL: Base agar....................................................... 65.0mL Horse serum .................................................. 20.0mL Yeast dialysate .............................................. 10.0mL Penicillin solution ........................................... 2.0mL MES (2-N-Morpholinoethane sulfonic acid) buffer solution ................... 1.0mL Na2SO3 solution.............................................. 1.0mL Urea solution................................................... 0.5mL pH 5.5 ± 0.2 at 25°C
Base Agar: Composition per liter: Papaic digest of soybean meal..........................20.0g Agarose .............................................................10.0g NaCl....................................................................5.0g Phenol Red (2% solution)............................... 1.0mL
Preparation of Base Agar: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Adjust pH to 7.3. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
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U9 Broth
Yeast Dialysate: Composition per 10.0mL:
U9 Broth (Urease Color Test Medium)
Yeast, active dried ...........................................450.0g
Composition per 101.6mL:
Preparation of Yeast Dialysate: Add active,
U9 base ......................................................... 95.0mL Horse serum, unheated.................................... 5.0mL Penicillin G solution ....................................... 1.0mL Urea solution................................................... 0.5mL Phenol Red solution........................................ 0.1mL pH 6.0 ± 0.2 at 25°C
dried yeast to distilled/deionized water and bring volume to 1250.0mL. Gently heat and bring to 40°C. Autoclave for 15 min at 15 psi pressure–121°C. Put into dialysis tubing. Dialyze against 1.0L of distilled/ deionized water for 2 days at 4°C. Discard tubing and its contents. Autoclave dialysate for 15 min at 15 psi pressure–121°C. Store at −20°C.
Penicillin Solution: Composition per 10.0mL: Penicillin ....................................................100,000U
Preparation of Penicillin Solution: Add penicillin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
MES Buffer Solution: Composition per 100.0mL: MES (2-N-Morpholinoethane sulfonic acid) buffer .................................19.52g
Preparation of MES Buffer Solution: Add MES buffer to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Adjust pH to 5.5. Filter sterilize.
Na2SO3 Solution: Composition per 10.0mL: Na2SO3 ............................................................0.126g
Preparation of Na2SO3 Solution: Add Na2SO3
to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Urea Solution: Composition per 100.0mL:
U9 Base: Composition per 100.0mL: NaCl..................................................................0.63g Pancreatic digest of casein..............................0.425g Papaic digest of soybean meal........................0.075g K2HPO4...........................................................0.063g Glucose ...........................................................0.063g KH2PO4.............................................................0.02g
Preparation of U9 Base: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Adjust pH to 5.5 with 1N HCl. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Penicillin G Solution: Composition per 10.0mL: Penicillin G ......................................................0.63 g
Preparation of Penicillin G Solution: Add penicillin G to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Urea Solution: Composition per 30.0mL: Urea.....................................................................3.0g
Preparation of Urea Solution: Add urea to distilled/deionized water and bring volume to 30.0mL. Mix thoroughly. Filter sterilize.
Urea.....................................................................6.0g
Phenol Red Solution: Composition per 10.0mL:
Preparation of Urea Solution: Add urea to dis-
Phenol Red..........................................................0.1g
tilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation of Phenol Red Solution: Add Phe-
Preparation of Medium: To 65.0mL of cooled, sterile base agar, aseptically add 10.0mL of sterile yeast dialysate, 20.0mL of horse serum, 2.0mL of sterile penicillin solution, 1.0mL of sterile MES buffer solution, 1.0mL of sterile Na2SO3 solution, and 0.5mL of sterile urea solution. Mix thoroughly. Pour into 10mm × 35mm Petri dishes in 5.0mL volumes. Allow plates to stand overnight at 25°C to remove excess surface moisture. Use within 48h.
Use: For the isolation and cultivation of Ureaplasma urealyticum.
nol Red to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: To 95.0mL of cooled, sterile U9 base, aseptically add 5.0mL of sterile horse serum, 1.0mL of sterile penicillin G solution, 0.5mL of sterile urea solution, and 0.1mL of sterile Phenol Red solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the isolation and identification of T-strain mycoplasmas from clinical specimens, especially Ureaplasma urealyticum. T-mycoplasmas are the only members of the Mycoplasma group known to
U9B Broth contain urease. Bacteria with urease activity turn the medium dark pink.
U9 Broth with Amphotericin B Composition per 101.6mL: U9 base ......................................................... 95.0mL Horse serum, unheated.................................... 5.0mL Antibiotic solution .......................................... 1.0mL Urea solution................................................... 0.5mL Phenol Red solution ........................................ 0.1mL pH 6.0 ± 0.2 at 25°C
U9 Base: Composition per 100.0mL: NaCl ..................................................................0.63g Pancreatic digest of casein ..............................0.425g Papaic digest of soybean meal ........................0.075g K2HPO4 ...........................................................0.063g Glucose ...........................................................0.063g KH2PO4 .............................................................0.02g
Preparation of U9 Base: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Adjust pH to 5.5 with 1N HCl. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Antibiotic Solution: Composition per 10.0mL: Penicillin G .......................................................0.63g Amphotericin B................................................2.5mg
Preparation of Antibiotic Solution: Add penicillin G and amphotericin B to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Urea Solution: Composition per 30.0mL: Urea.....................................................................3.0g
Preparation of Urea Solution: Add urea to distilled/deionized water and bring volume to 30.0mL. Mix thoroughly. Filter sterilize.
Phenol Red Solution: Composition per 10.0mL: Phenol Red..........................................................0.1g
Preparation of Phenol Red Solution: Add Phenol Red to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: To 95.0mL of cooled, sterile U9 base, aseptically add 5.0mL of sterile horse serum, 1.0mL of sterile antibiotic solution, 0.5mL of sterile urea solution, and 0.1mL of sterile Phenol Red solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
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Use: For the isolation and identification of T-strain mycoplasmas from clinical specimens, especially Ureaplasma urealyticum. T-mycoplasmas are the only members of the Mycoplasma group known to contain urease. Bacteria with urease activity turn the medium dark pink.
U9B Broth Composition per 102.1mL: U9 base ......................................................... 95.0mL Horse serum, unheated.................................... 5.0mL Penicillin G solution ....................................... 1.0mL Urea solution................................................... 0.5mL L-Cysteine·HCl·H2O solution ......................... 0.5mL Phenol Red solution........................................ 0.1mL pH 6.0 ± 0.2 at 25°C
U9 Base: Composition per 100.0mL: NaCl..................................................................0.63g Pancreatic digest of casein..............................0.425g Papaic digest of soybean meal........................0.075g K2HPO4...........................................................0.063g Glucose ...........................................................0.063g KH2PO4.............................................................0.02g
Preparation of U9 Base: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Adjust pH to 5.5 with 1N HCl. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C.
Penicillin G Solution: Composition per 10.0mL: Penicillin G ......................................................0.63 g
Preparation of Penicillin G Solution: Add penicillin G to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Urea Solution: Composition per 30.0mL: Urea.....................................................................3.0g
Preparation of Urea Solution: Add urea to distilled/deionized water and bring volume to 30.0mL. Mix thoroughly. Filter sterilize. L-Cysteine·HCl·H2O
Solution: Composition per 50.0mL: L-Cysteine·HCl·H2O ...........................................1.0g
Preparation of L-Cysteine·HCl·H2O Solution: Add urea to distilled/deionized water and bring volume to 50.0mL. Mix thoroughly. Filter sterilize.
Phenol Red Solution: Composition per 10.0mL: Phenol Red..........................................................0.1g
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U9C Broth
Preparation of Phenol Red Solution: Add Phe-
Preparation of Urea Solution: Add urea to dis-
nol Red to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
tilled/deionized water and bring volume to 30.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: To 95.0mL of cooled,
L-Cysteine·HCl·H2O
sterile U9 base, aseptically add 5.0mL of sterile horse serum, 1.0mL of sterile penicillin G solution, 0.5mL of sterile urea solution, 0.5mL of sterile L-cysteine·HCl·H2O solution, and 0.1mL of sterile Phenol Red solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the isolation and identification of T-strain mycoplasmas from clinical specimens, especially Ureaplasma urealyticum. T-mycoplasmas are the only members of the Mycoplasma group known to contain urease. Bacteria with urease activity turn the medium dark pink.
U9C Broth Composition per 102.0mL: U9C base....................................................... 90.0mL Horse serum, unheated.................................. 10.0mL Penicillin G solution ....................................... 1.0mL L-Cysteine·HCl·H2O solution ......................... 0.5mL Urea solution................................................... 0.3mL GHL tripeptide solution .................................. 0.1mL Phenol Red solution ........................................ 0.1mL pH 6.0 ± 0.2 at 25°C
U9C Base: Composition per 100.0mL: NaCl ..................................................................0.85g Pancreatic digest of casein................................0.25g Papaic digest of soybean meal ..........................0.15g K2HPO4 .............................................................0.12g Glucose .............................................................0.12g MgCl2·6H2O .......................................................0.2g Yeast extract........................................................0.1g KH2PO4 .............................................................0.02g
Preparation of U9C Base: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Adjust pH to 5.5 with 2N HCl. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Penicillin G Solution: Composition per 10.0mL: Penicillin G ......................................................0.63 g
Preparation of Penicillin G Solution: Add penicillin G to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Urea Solution: Composition per 30.0mL: Urea.....................................................................3.0g
Solution: Composition per 50.0mL: L-Cysteine·HCl·H2O ...........................................1.0g
Preparation of L-Cysteine·HCl·H2O Solution: Add urea to distilled/deionized water and bring volume to 50.0mL. Mix thoroughly. Filter sterilize.
GHL Tripeptide Solution: Composition per 10.0mL: GHL tripeptide.................................................0.2mg
Preparation of GHL Tripeptide Solution: Add GHL tripeptide (glycyl-L-histidyl-L-lysine acetate) to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Phenol Red Solution: Composition per 10.0mL: Phenol Red..........................................................0.1g
Preparation of Phenol Red Solution: Add Phenol Red to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: To 90.0mL of cooled, sterile U9C base, aseptically add 10.0mL of sterile horse serum, 1.0mL of sterile penicillin G solution, 0.3mL of sterile urea solution, 0.5mL of sterile L-cysteine·HCl·H2O solution, 0.1mL of sterile GHL tripeptide solution, and 0.1mL of sterile Phenol Red solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the isolation and identification of T-strain mycoplasmas from clinical specimens, especially Ureaplasma urealyticum. T-mycoplasmas are the only members of the Mycoplasma group known to contain urease. Bacteria with urease activity turn the medium dark pink.
Urea Agar (Urease Test Agar) (Urea Agar Base, Christensen) Composition per liter: Urea...................................................................20.0g Agar ..................................................................15.0g NaCl....................................................................5.0g KH2PO4...............................................................2.0g Peptone ...............................................................1.0g Glucose ...............................................................1.0g Phenol Red......................................................0.012g pH 6.8 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Urea Broth 10B for Ureaplasma urealyticum Preparation of Medium: Add components, except agar, to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize. Add agar to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C. Aseptically add the 100.0mL of sterile basal medium. Mix thoroughly. Distribute into sterile tubes. Allow tubes to solidify in a slanted position.
Use: For the differentiation of a variety of microorganisms, especially members of the Enterobacteriaceae, aerobic actinomycetes, streptococci, and nonfermenting Gram-negative bacteria, on the basis of urease production.
Urea Agar Base Composition per liter:
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Horse serum, unheated.................................. 20.0mL Fresh yeast extract solution .......................... 10.0mL L-Cysteine·HCl·H2O........................................ 0.5mL CVA enrichment ............................................. 0.5mL Urea solution................................................... 0.4mL Phenol Red...................................................... 0.1mL
PPLO Broth without Crystal Violet: Composition per 900.0mL: Beef heart, solids from infusion........................16.1g Peptone .............................................................3.25g NaCl..................................................................1.61g
Preparation of PPLO Broth without Crystal Violet: Add components to distilled/deionized water and bring volume to 900.0mL. Adjust pH to 5.5 with 2N HCl. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 37°C.
Fresh Yeast Extract Solution: Composition per 100.0mL:
Agar ..................................................................15.0g NaCl ....................................................................5.0g Na2HPO4 .............................................................1.2g Peptone................................................................1.0g Glucose ...............................................................1.0g KH2PO4 ...............................................................0.8g Phenol Red......................................................0.012g Urea solution................................................. 50.0mL pH 6.8 ± 0.2 at 25°C
Preparation of Fresh Yeast Extract Solution: Add the live Baker’s yeast to 100.0mL of distilled/ deionized water. Autoclave for 90 min at 15 psi pressure–121°C. Allow to stand. Remove supernatant solution. Adjust pH to 6.6–6.8.
Source: This medium is available as a premixed powder from Oxoid Unipath.
L-Cysteine·HCl·H2O ...........................................1.0g
Urea Solution: Composition per 100.0mL: Urea...................................................................40.0g
Preparation of Urea Solution: Add urea to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except urea solution, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 20 min at 10 psi pressure–115°C. Cool to 50°C. Aseptically add 50.0mL of sterile urea solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes. Allow tubes to solidify in a slanted position.
Use: For the detection of Proteus species based on rapid urease activity and the identification of other members of the Enterobacteriaceae based on urease activity. Urease-positive bacteria turn the medium pink.
Urea Broth 10B for Ureaplasma urealyticum
Baker’s yeast live, pressed, starch-free.............25.0g
L-Cysteine·HCl·H2O
Solution: Composition per 50.0mL: Preparation of L-Cysteine·HCl·H2O Solution: Add L-cysteine·HCl·H2O to distilled/deionized
water and bring volume to 50.0mL. Mix thoroughly. Filter sterilize.
CVA Enrichment: Composition per liter: Glucose ...........................................................100.0g L-Cysteine·HCl·H2O..........................................25.9g L-Glutamine ......................................................10.0g Adenine...............................................................1.0g L-Cystine·2HCl ...................................................1.0g Nicotinamide adenine dinucleotide ..................0.25g Cocarboxylase.....................................................0.1g Guanine·HCl .....................................................0.03g Fe(NO3)3 ...........................................................0.02g p-Aminobenzoic acid......................................0.013g Vitamin B12 .......................................................0.01g Thiamine·HCl ..................................................3.0mg
Preparation of CVA Enrichment: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
Composition per 100.5mL:
Urea Solution: Composition per 30.0mL:
PPLO broth without Crystal Violet............... 70.0mL
Urea.....................................................................3.0g
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Urea Broth Base
Preparation of Urea Solution: Add urea to dis-
Source: This medium is available as a prepared me-
tilled/deionized water and bring volume to 30.0mL. Mix thoroughly. Filter sterilize.
dium from BD Diagnostic Systems.
Preparation of Medium: Aseptically combine
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize. Aseptically distribute into sterile tubes or flasks.
the components, except the PPLO broth without Crystal Violet. Aseptically add this mixture to the cooled, sterile PPLO broth without Crystal Violet. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation and maintenance of Ureaplasma urealyticum and other Ureaplasma species. Urease-positive bacteria turn the medium to peach orange.
Urea Broth Base Composition per liter: NaCl ....................................................................5.0g Na2HPO4 .............................................................1.2g Peptone................................................................1.0g Glucose ...............................................................1.0g KH2PO4 ...............................................................0.8g Phenol Red......................................................0.012g Urea solution................................................. 50.0mL pH 6.8 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath. Urea Solution: Composition per 100.0mL: Urea...................................................................40.0g
Preparation of Urea Solution: Add urea to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, ex-
Preparation of Medium: Add components to
Use: For the differentiation of members of the Enterobacteriaceae based on the rapid detection of urease activity. Urease-positive bacteria turn the medium cerise.
Urea Semisolid Medium Composition per liter: Solution A................................................... 400.0mL Solution B ..................................................... 50.0mL
Solution A: Composition per 400.0mL: Pancreatic digest of casein..................................6.0g Yeast extract........................................................2.8g NaCl....................................................................1.0g Agar ....................................................................0.3g L-Cystine .............................................................0.1g Thioglycollic acid ......................................... 0.12mL pH 7.2 ± 0.2 at 25°C
Preparation of Solution A: Add components to distilled/deionized water and bring volume to 400.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 60°C. Solution B: Composition per 50.0mL:
cept urea solution, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Autoclave for 20 min at 10 psi pressure–115°C. Cool to 50°C. Aseptically add 50.0mL of sterile urea solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Urea.....................................................................8.0g Na2HPO4 .............................................................3.8g KH2PO4.............................................................3.64g Yeast extract......................................................0.04g Phenol Red.......................................................4.0mg
Use: For the differentiation of members of the Enter-
Preparation of Solution B: Add components to
obacteriaceae based on urease production. Ureasepositive bacteria turn the medium pink.
distilled/deionized water and bring volume to 50.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Aseptically combine
Urea R Broth (Urea Rapid Broth) Composition per liter: Urea...................................................................20.0g Yeast extract........................................................0.1g Na2HPO4 .........................................................0.095g KH2PO4 ...........................................................0.091g Phenol Red........................................................0.01g pH 6.9 ± 0.2 at 25°C
400.0mL of sterile solution A and 50.0mL of sterile solution B. Mix thoroughly. Aseptically distribute into sterile screw-capped tubes in 7.0mL volumes. Pass the tubes into an anaerobic chamber containing 85% N2 + 10% H2 + 5% CO2 for 60 min. Close screw caps tightly.
Use: For the cultivation and differentiation of anaerobic bacteria based on their production of urease. Bacteria that produce urease turn the medium bright red.
Urease Test Broth
Urea Test Broth Composition per liter: Urea...................................................................20.0g Na2HPO4 .............................................................9.5g KH2PO4 ...............................................................9.1g Yeast extract........................................................0.1g Phenol Red........................................................0.01g Urea solution............................................... 100.0mL
Urea Solution: Composition per 100.0mL: Urea...................................................................20.0g
Preparation of Urea Solution: Add urea to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except urea solution, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile urea solution. Mix thoroughly. Aseptically distribute into sterile tubes in 3.0mL volumes.
Use: For the cultivation and differentiation of members of the Enterobacteriaceae and aerobic actinomycetes based on their production of urease. Bacteria that produce urease turn the medium bright red.
Urea Test Broth Composition per 99.6mL: H broth base .................................................. 85.0mL Horse serum .................................................. 10.0mL Penicillin solution ........................................... 2.0mL MES (2-N-Morpholinoethane sulfonic acid) buffer solution.................... 1.0mL Na2SO3 solution.............................................. 1.0mL Urea solution................................................... 0.5mL Phenol Red solution ........................................ 0.1mL pH 7.2 ± 0.2 at 25°C
H Broth Base: Composition per liter: NaCl ....................................................................5.0g Pancreatic digest of casein..................................5.0g Peptone................................................................5.0g Beef extract .........................................................3.0g K2HPO4 ...............................................................2.5g Glucose ...............................................................1.0g
Preparation of H Broth Base: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes in 4.0mL volumes. Autoclave for 15 min at 10 psi pressure–115°C. Cool to 45°–50°C.
467
Penicillin Solution: Composition per 10.0mL: Penicillin .................................................... 100,000U
Preparation of Penicillin Solution: Add penicillin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
MES Buffer Solution: Composition per 100.0mL: MES (2-N-Morpholinoethane sulfonic acid) buffer .................................19.52g
Preparation of MES Buffer Solution: Add MES buffer to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Adjust pH to 5.5. Filter sterilize.
Na2SO3 Solution: Composition per 10.0mL: Na2SO3 ............................................................0.126g
Preparation of Na2SO3 Solution: Add Na2SO3
to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Urea Solution: Composition per 100.0mL: Urea.....................................................................6.0g
Preparation of Urea Solution: Add urea to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Phenol Red Solution: Composition per 10.0mL: Phenol Red..........................................................0.1g
Preparation of Phenol Red Solution: Add Phenol Red to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: To 85.0mL of cooled sterile H broth base, aseptically add 10.0mL of sterile horse serum, 2.0mL of sterile penicillin solution, 1.0mL of MES buffer solution, 1.0mL of Na2SO3 solution, 0.5mL of urea solution, and 0.1 mL of sterile Phenol Red solution. Mix thoroughly. Aseptically distribute into test tubes in 3.0mL volumes. Use: For the cultivation and differentiation of Ureaplasma species based on their production of urease.
Urease Test Broth (Urea Broth) Composition per liter: Urea...................................................................20.0g Na2HPO4 .............................................................9.5g KH2PO4...............................................................9.1g
468
UVM Listeria Enrichment Broth
Yeast extract........................................................0.1g Phenol Red........................................................0.01g pH 6.8 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Source: This medium is available as a premixed
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize. Aseptically distribute into sterile tubes or flasks.
Preparation of Medium: Add components to
Use: For the selective isolation of Listeria monocytogenes.
V Agar
Use: For the differentiation of organisms, especially the Enterobacteriaceae, on the basis of urease production. Urease-positive bacteria turn the medium pink.
UVM Listeria Enrichment Broth (University of Vermont Listeria Enrichment Broth) Composition per liter: NaCl ..................................................................20.0g Na2HPO4 .............................................................9.6g Pancreatic digest of casein..................................5.0g Peptic digest of animal tissue..............................5.0g Beef extract .........................................................5.0g Yeast extract........................................................5.0g KH2PO4 .............................................................1.35g Esculin ................................................................1.0g Nalidixic acid .................................................40.0mg Acriflavine·HCl..............................................12.0mg pH 7.2 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the selective isolation of Listeria monocytogenes.
UVM Modified Listeria Enrichment Broth (University of Vermont Modified Listeria Enrichment Broth) Composition per liter: NaCl ..................................................................20.0g Na2HPO4 .............................................................9.6g Pancreatic digest of casein..................................5.0g Peptic digest of animal tissue..............................5.0g Beef extract .........................................................5.0g Yeast extract........................................................5.0g KH2PO4 .............................................................1.35g Esculin ................................................................1.0g Nalidixic acid .................................................20.0mg Acriflavine·HCl..............................................12.0mg pH 7.2 ± 0.2 at 25°C
Composition per liter: Agar ..................................................................13.5g Pancreatic digest of casein................................12.0g Peptone .............................................................10.0g Peptic digest of animal tissue .............................5.0g NaCl....................................................................5.0g Beef extract.........................................................3.0g Yeast extract........................................................3.0g Cornstarch...........................................................1.0g Human blood, anticoagulated ....................... 50.0mL pH 7.4 ± 0.2 at 25°C
Source: This medium is available as a prepared medium from BD Diagnostic Systems.
Preparation of Medium: Add components, except human blood, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 50°C. Aseptically add 50.0mL of human blood. Mix thoroughly. Pour into sterile Petri dishes or leave in tubes.
Use: For the isolation and differentiation of Gardnerella vaginalis from clinical specimens. Plates are incubated under an atmosphere with 3-10% CO2. Gardnerella vaginalis appears as small white colonies with diffuse β-hemolysis.
V-8™ Agar Composition per liter: Agar ..................................................................20.0g CaCO3 .................................................................4.0g V-8 canned vegetable juice ......................... 200.0mL pH 7.3 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the isolation and cultivation of Actinomadura species.
Veillonella Agar
V-8 Agar Composition per liter: Agar ..................................................................15.0g CaCO3 .................................................................2.0g V-8 canned vegetable juice ......................... 200.0mL
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation of numerous yeasts and filamentous fungi.
Veal Infusion Agar Composition per liter: Agar ..................................................................15.0g Veal, infusion from ...........................................10.0g Pancreatic digest of casein..................................5.0g Peptic digest of animal tissue..............................5.0g NaCl ....................................................................5.0g pH 7.4 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of a variety of microorganisms. Can be used for the cultivation of fastidious microorganisms when enriched with blood or serum.
Veal Infusion Agar (ATCC Medium 521) Composition per liter: Veal, infusion from .........................................500.0g Agar ..................................................................15.0g Pancreatic digest of casein..................................5.0g Peptic digest of animal tissue..............................5.0g NaCl ....................................................................5.0g pH 7.4 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min
469
at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of a variety of microorganisms. Can be used for the cultivation of fastidious microorganisms when enriched with blood or serum.
Veal Infusion Broth Composition per liter: Veal, infusion from ...........................................10.0g Pancreatic digest of casein..................................5.0g Peptic digest of animal tissue .............................5.0g NaCl....................................................................5.0g pH 7.4 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Use freshly prepared solution.
Use: For the cultivation of streptococci and other microorganisms.
Veal Infusion Broth with Horse Serum Composition per liter: Veal, infusion from .........................................500.0g Pancreatic digest of casein..................................5.0g Peptic digest of animal tissue .............................5.0g NaCl....................................................................5.0g Horse serum, heat inactivated..................... 100.0mL pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components, except horse serum, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C. Aseptically add 100.0mL of horse serum. Mix thoroughly. Aseptically distribute into tubes or flasks. Use freshly prepared solution or boil without mixing prior to use.
Use: For the cultivation and maintenance of Streptococcus pyogenes.
Veillonella Agar Composition per liter: Agar ..................................................................15.0g Pancreatic digest of casein..................................5.0g Yeast extract........................................................3.0g Sodium thioglycolate ........................................0.75g Vancomycin .....................................................7.5mg
470
Veillonella Medium
Basic Fuchsin...................................................2.0mg Sodium lactate (60% solution)...................... 21.0mL pH 7.5± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Caution: Basic Fuchsin is a potential carcinogen and care must be taken to avoid inhalation of the powdered dye and contact with the skin.
Preparation of Medium: Add components, except vancomycin, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C. Aseptically add vancomycin. Mix thoroughly. Pour into sterile Petri dishes or leave in tubes.
Use: For the selective isolation and cultivation of Veillonella species.
Veillonella Medium Composition per liter: Pancreatic digest of casein..................................5.0g Yeast extract........................................................3.0g Tween 80.............................................................1.0g Glucose ...............................................................1.0g Sodium thioglycolate ........................................0.75g Sodium lactate (60% solution)...................... 21.0mL pH 7.5 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.5 with K2CO3. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation and maintenance of Veillonella species.
Veillonella Medium, DSM Composition per liter: Sodium lactate (60% solution)............................7.5g Pancreatic digest of casein ..................................5.0g Yeast extract........................................................3.0g Tween 80.............................................................1.0g Glucose ...............................................................1.0g Sodium thioglycolate ........................................0.75g Putrescine.........................................................3.0mg Resazurin .........................................................1.0mg pH 7.5 ± 0.2 at 25°C
Preparation of Medium: Prepare and dispense medium anaerobically under 100% N2. Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.5 with K2CO3. Anaerobically distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation and maintenance of Veillonella parvula and other Veillonella species.
Veillonella Selective Medium Composition per liter: Pancreatic digest of casein..................................5.0g Yeast extract........................................................3.0g Tween 80.............................................................1.0g Sodium thioglycolate ........................................0.75g Sodium lactate (50% solution)...................... 25.0mL Streptomycin solution ................................... 10.0mL pH 6.6 ± 0.2 at 25°C
Streptomycin Solution: Composition per 10.0mL: Streptomycin....................................................5.0mg
Preparation of Streptomycin Solution: Add streptomycin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. Preparation of Medium: Add components, except streptomycin solution, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Adjust pH to 6.6 with K2CO3. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile streptomycin solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the cultivation of Veillonella species.
Vibrio Agar Composition per liter: Sucrose..............................................................20.0g Agar ..................................................................15.0g NaCl..................................................................10.0g Sodium citrate·2H2O.........................................10.0g Na2S2O3·5H2O ....................................................6.5g Oxgall .................................................................5.0g Yeast extract........................................................5.0g Pancreatic digest of casein..................................4.0g Proteose peptone.................................................3.0g Sodium deoxycholate..........................................1.0g Sodium lauryl sulfate..........................................0.2g Water Blue ..........................................................0.2g Cresol Red ........................................................0.02g pH 8.5 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 8.5. Gently heat and bring to boiling. Do not autoclave. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the isolation and cultivation of the Vibrio cholerae.
Vitamin B6 Blood Agar
Vibrio parahaemolyticus Sucrose Agar (VPSA) Composition per liter:
471
NaCl....................................................................5.0g Pancreatic digest of casein..................................5.0g Peptic digest of animal tissue .............................5.0g
NaCl ..................................................................30.0g Agar ..................................................................15.0g Sucrose..............................................................10.0g Yeast extract........................................................7.0g Tryptose ..............................................................5.0g Pancreatic digest of casein..................................5.0g Bile salts no. 3.....................................................1.5g Bromthymol Blue ...........................................0.025g pH 8.6 ± 0.2 at 25°C
Preparation of Veal Infusion Broth: Add com-
Preparation of Medium: Add components to dis-
Preparation of Amphotericin B Solution:
tilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Do not autoclave. Cool to 50°C. Pour into sterile Petri dishes in 20.0mL volumes. Allow plates to dry before using.
Use: For the isolation, cultivation, and differentiation of Vibrio parahaemolyticus. Vibrio parahaemolyticus and Vibrio vulnificus appear as blue to green colonies. Other Vibrio species appear as yellow colonies.
Violet Peptone Bile Lactose Broth Composition per liter: Lactose ..............................................................10.0g Peptone..............................................................10.0g Bile salts..............................................................5.0g Gentian Violet ...................................................0.04g pH 7.6 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the selective cultivation of members of the
ponents to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure– 121°C. Use freshly prepared solution.
Amphotericin B Solution: Composition per 10.0mL: Amphotericin B ..................................................2.5g Add amphotericin B to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Gentamicin Solution: Composition per 10.0mL: Gentamicin..........................................................0.5g
Preparation of Gentamicin Solution: Add gentamicin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Vancomycin Solution: Composition per 10.0mL: Vancomycin ........................................................0.5g
Preparation of Vancomycin Solution: Add vancomycin to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize. Preparation of Medium: To 100.0mL of sterile veal infusion broth, aseptically add bovine serum albumin, Phenol Red, amphotericin B solution, gentamicin solution, and vancomycin solution. Mix thoroughly. Dispense 2.0mL of medium into serum vials. Store at 4°C and use for up to 2 months.
Use: For the maintenance and transport of specimens suspected of being virally infected.
Enterobacteriaceae.
Viral Transport Medium (VTM) Composition per 104.1mL: Bovine serum albumin ........................................0.5g Veal infusion broth...................................... 100.0mL Amphotericin B solution................................. 2.0mL Gentamicin...................................................... 1.0mL Phenol Red...................................................... 0.4mL Vancomycin .................................................... 0.2mL pH 7.4 ± 0.2 at 25°C
Veal Infusion Broth: Composition per liter: Veal, infusion from .........................................500.0g
Vitamin B6 Blood Agar (ATCC Medium 860) Composition per liter: Agar ..................................................................15.0g Pancreatic digest of casein................................15.0g Papaic digest of soybean meal............................5.0g NaCl....................................................................5.0g Sheep blood, defibrinated ............................. 50.0mL pH 7.3 ± 0.2 at 25°C
Preparation of Medium: Add components, except sheep blood, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add
472
Vitamin B6 Blood Agar with Pyridoxal-HCl
sterile, defibrinated sheep blood. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation and maintenance of fastidious microorganisms, especially Streptococcus species.
Vitamin B6 Blood Agar with PyridoxalHCl (ATCC Medium 1511) Composition per liter: Agar ..................................................................15.0g Pancreatic digest of casein................................15.0g Papaic digest of soybean meal ............................5.0g NaCl ....................................................................5.0g Pyridoxal·HCl ...................................................0.01g Sheep blood, defibrinated ............................. 50.0mL pH 7.3 ± 0.2 at 25°C
Campylobacter fetus, Campylobacter hyointestinalis, Campylobacter jejuni, Campylobacter lari, Campylobacter mucosalis, Campylobacter species, Campylobacter sputorum, Capnocytophaga gingivalis, Capnocytophaga ochracea, Capnocytophaga sputigena, Clostridium colinum, Clostridium difficile, Clostridium species, Clostridium spiroforme, Falcivibrio grandis, Falcivibrio vaginalis, Fusobacterium simiae, Gardnerella vaginalis, Leptotrichia buccalis, Pectinatus frisingensis, Peptostreptococcus anaerobius, Peptostreptococcus asaccharolyticus, Peptostreptococcus indolicus, Peptostreptococcus magnus, Peptostreptococcus micros, Peptostreptococcus prevotii, Peptostreptococcus tetradius, Propionibacterium acnes, Propionibacterium avidum, Propionibacterium granulosum, Propionibacterium lymphophilum, and Tonsillophilus suis.
Preparation of Medium: Add components, except sheep blood, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile, defibrinated sheep blood. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation and maintenance of fastidious microorganisms, especially Streptococcus species.
VL Agar with Blood Composition per liter: Agar ..................................................................20.0g Tryptone ............................................................10.0g NaCl ....................................................................5.0g Yeast extract........................................................5.0g Beef extract .........................................................2.0g Glucose ...............................................................2.0g L-Cysteine·HCl ...................................................0.3g Sheep blood or horse blood ........................ 100.0mL pH 7.4 ± 0.2 at 25°C
Preparation of Medium: Add components, except sheep blood, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Adjust pH to 7.4. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Warm sheep blood to 50°C. Aseptically add 100.0mL of sterile sheep blood or 100.0mL of sterile horse blood. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
Use: For the cultivation and maintenance of Bacterionema helcogenes, Bacteroides nodosus, Bacteroides pyogenes, Bacteroides salivosus, Bacteroides suis, Bifidobacterium adolescentis, Bifidobacterium bifidum, Bifidobacterium breve, Bifidobacterium longum, Campylobacter coli, Campylobacter concisus,
VL Medium Composition per liter: Pancreatic digest of casein................................10.0g Agar ....................................................................6.0g NaCl....................................................................5.0g Yeast extract........................................................5.0g Meat extract ........................................................2.0g Glucose ...............................................................2.0g L-Cysteine·HCl·H2O ...........................................0.3g Antibiotic solution ........................................ 10.0mL pH 7.4 ± 0.2 at 25°C
Antibiotic Solution: Composition per 10.0mL: Kanamycin..........................................................0.1g Vancomycin .....................................................7.5mg
Preparation of Antibiotic Solution: Add components to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except antibiotic solution, to distilled/deionized water and bring volume to 990.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add sterile antibiotic solution. Mix thoroughly. Aseptically distribute into sterile tubes or flasks.
Use: For the isolation and cultivation of Bacteroides species.
Vogel and Johnson Agar Composition per liter: Agar ..................................................................16.0g Pancreatic digest of casein................................10.0g D-Mannitol ........................................................10.0g Glycine..............................................................10.0g
VRE Agar Yeast extract........................................................5.0g K2HPO4 ...............................................................5.0g LiCl .....................................................................5.0g Phenol Red......................................................0.025g K2TeO3 solution ............................................ 20.0mL pH 7.2 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems and Oxoid Unipath.
K2TeO3 Solution: Composition per 100.0mL: K2TeO3 ................................................................1.0g
Preparation of K2TeO3 Solution: Add K2TeO3
to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Caution: Potassium tellurite is toxic. Preparation of Medium: Add components, except K2TeO3 solution, to distilled/deionized water and bring volume to 980.0mL. Mix thoroughly. Gently heat and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 45°–50°C. Aseptically add 20.0mL of sterile K2TeO3 solution. Mix thoroughly. Pour into sterile Petri dishes or distribute into sterile tubes.
473
Neutral Red.......................................................0.03g Crystal Violet ..................................................0.002g pH 7.4 ± 0.2 at 25°C
Source: This medium is available from Merck. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Heat in a boiling water bath or in free flowing steam with frequent stirring until completely dissolved. Do not boil for more than 2 min. Do not autoclave. Do not overheat. Pour into sterile Petri dishes. The plates are clear and dark red.
Use: For the detection and enumeration of coliform bacteria, in particular E. coli. Crystal violet and bile salts largely inhibit the growth of Gram-positive accompanying bacterial flora. Lactose-postitive colonies show a color change to red of the pH indicator. E. coli colonies schow a fluorescence under UV light. Lactose-negative Enterobacteriaceae are colorless. Lactose-positive colonies are red and often surrounded by a turbid zone due to the precipitation of bile acids. Light blue fluorescing colonies denote E. coli.
VRB MUG Agar (Violet Red Bile Lactose MUG Agar)
Use: For the detection of coagulase-positive Staphy-
Composition per liter:
lococcus aureus.
Peptone................................................................7.0g K2HPO4 ...............................................................5.0g Glucose ...............................................................5.0g pH 6.9 ± 0.2 at 25°C
Agar ..................................................................13.0g Lactose..............................................................10.0g Meat peptone ......................................................7.0g NaCl....................................................................5.0g Yeast extract........................................................3.0g Bile salt mixture..................................................1.5g 4-Methylumbelliferyl-β-D-glucuronide ..............0.1g Neutral Red.......................................................0.03g Crystal Violet ..................................................0.002g pH 7.4 ± 0.2 at 37°C
Preparation of Medium: Add components to
Source: This medium is available from Fluka, Sig-
VP Medium (Voges-Proskauer Medium) Composition per liter:
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 6.9. Distribute into tubes in 3.0mL volumes. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation and differentiation of bacteria based on their ability to produce acetoin.
VRB Agar, Fluorocult (Fluorocult VRB Agar) Composition per liter: Agar ..................................................................13.0g Lactose ..............................................................10.0g Peptone from meat ..............................................7.0g NaCl ....................................................................5.0g Yeast extract........................................................3.0g Bile salt mixture..................................................1.5g 4-Methylumbelliferyl-β-D-glucuronide ..............0.1g
ma-Aldrich.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 50°C. Pour into sterile Petri dishes.
Use: For the detection and enumeration of coliform bacteria, in particular E. coli. Gram-positive accompanying flora are extensively inhibited by Crystal Violet and bile salts. A color-change to red indicates lactose-positive colonies, within which E. coli can be demonstrated by fluorescence in the UV.
VRE Agar Composition per 1004mL: Tryptone............................................................20.0g
474
VRE Agar
Agar ..................................................................10.0g Yeast extract........................................................5.0g NaCl ....................................................................5.0g Sodium citrate .....................................................1.0g Aesculin ..............................................................1.0g Ferric ammonium citrate.....................................0.5g NaN3 .................................................................0.15g Selective supplement solution ........................ 4.0mL pH 7.0 ± 0.2 at 25°C
Selective Supplement Solution: Composition per 4.0mL:
Source: This medium is available as a premixed
cept selective supplement solution, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 50°C. Aseptially add 4.0mL selective supplement solution. Mix thoroughly. Pour into sterile Petri dishes.
powder from Oxoid Unipath.
Selective Supplement Solution: Composition per 4.0mL: Meropenum......................................................1.0mg Vancomycin .....................................................6.0mg
Preparation of Selective Supplement Solution: Add components to distilled/deionized water and bring volume to 4.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except selective supplement solution, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 50°C. Aseptially add 4.0mL selective supplement solution. Mix thoroughly. Pour into sterile Petri dishes.
Use: For the isolation of vancomycin resistant enterococci (VRE) from clinical samples. Nonresitant enterococci containing the Van C genes will not grow on this medium.The selective supplement suppresses growth of Gram negative bacteria and E. gallinarum. The medium contains an indicator system to detect the growth of aesculin-hydrolysing organisms. Enterococci produce black zones around the colonies from the formation of black iron phenolic compounds derived from aesculin-hydrolyis products and ferrous iron.
VRE Agar Composition per 1004mL: Tryptone ............................................................20.0g Agar ..................................................................10.0g Yeast extract........................................................5.0g NaCl ....................................................................5.0g Sodium citrate .....................................................1.0g Aesculin ..............................................................1.0g Ferric ammonium citrate.....................................0.5g NaN3 .................................................................0.15g Selective supplement solution ........................ 4.0mL pH 7.0 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath.
Gentamicin...................................................512.0mg
Preparation of Selective Supplement Solution: Add gentamicin to distilled/deionized water and bring volume to 4.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, ex-
Use: For the isolation of high level aminoglycoside resistant enterococci (HLARE) from clinical samples. Nonresitant enterococci containing the Van C genes will not grow on this medium.The selective supplement suppresses growth of Gram negative bacteria and E. gallinarum. The medium contains an indicator system to detect the growth of aesculin-hydrolysing organisms. Enterococci produce black zones around the colonies from the formation of black iron phenolic compounds derived from aesculin-hydrolyis products and ferrous iron.
VRE Broth Composition per 1004mL: Calf brain infusion solids..................................12.5g Proteose peptone...............................................10.0g Beef heart infusion solids ...................................5.0g NaCl....................................................................5.0g Na2HPO4 .............................................................2.5g Glucose ...............................................................2.0g Selective supplement solution ........................ 4.0mL pH 7.4 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath.
Selective Supplement Solution: Composition per 4.0mL: Meropenum......................................................2.0mg
Preparation of Selective Supplement Solution: Add meropenum to distilled/deionized water and bring volume to 4.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except selective supplement solution, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat while stirring and bring to boiling. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 50°C. Aseptially add 4.0mL selective
Wickerham Broth
475
supplement solution. Mix thoroughly. Aseptically distribute into sterile tubes.
lution for 1 min. Crack eggs and separate yolks from whites. Mix egg yolks with 6 chicken eggs.
Use: For the isolation of high level aminoglycoside resistant enterococci (HLARE) from clinical samples. Nonresitant enterococci will not grow on this medium. The selective supplement suppresses growth of Gram negative bacteria and E. gallinarum.
Preparation of Medium: Add components to
Wagatsuma Agar Composition per 1050.0mL: NaCl ..................................................................70.0g Agar ..................................................................15.0g Mannitol............................................................10.0g Peptone..............................................................10.0g K2HPO4 ..............................................................5.0g Yeast extract........................................................3.0g Crystal Violet ...................................................1.0mg Red blood cells.............................................. 50.0mL pH 8.0 ± 0.2 at 25°C
Red Blood Cells: Composition per 100.0mL: Blood, human or rabbit ............................... 100.0mL
Preparation of Red Blood Cells: Mix freshly drawn human or rabbit blood with anticoagulant and an equal volume of sterile 0.85% saline solution. Centrifuge cells at 4000 × g at 4°C for 15 min. Pour off saline and wash two more times with sterile saline. After last wash, pour off saline and resuspend cells to their original volume.
Preparation of Medium: Add components, except blood, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 8.0. Place in a steam bath for 30 min. Do not autoclave. Cool to 45°–50°C. Add 50.0mL of washed red blood cells. Mix thoroughly. Pour into sterile Petri dishes. Dry plates before using.
Use: For the cultivation and detection of thermostable hemolysin of Vibrio parahaemolyticus by the Kanagawa reaction.
Wallerstein Medium Composition per 4.225L: Malachite Green................................................0.75g Egg yolk emulsion ......................................... 3.125L Glycerol ...................................................... 100.0mL pH 6.75 ± 0.2 at 25°C
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the isolation of Mycobacterium species other than Mycobacterium leprae.
Wickerham Broth Composition per 100.0mL: Carbohydrate.....................................................10.0g Yeast nitrogen base ..................................... 100.0mL
Yeast Nitrogen Base, 10X: Composition per liter: Glucose .............................................................10.0g KH2PO4...............................................................1.0g MgSO4·7H2O ......................................................0.5g NaCl....................................................................0.1g CaCl2·2H2O ........................................................0.1g DL-Methionine...................................................0.02g DL-Tryptophan...................................................0.02g L-Histidine·HCl .................................................0.01g Inositol .............................................................2.0mg H3BO3 ..............................................................0.5mg ZnSO4·7H2O ....................................................0.4mg MnSO4·4H2O ...................................................0.4mg Thiamine·HCl ..................................................0.4mg Pyridoxine........................................................0.4mg Niacin...............................................................0.4mg Calcium pantothenate ......................................0.4mg p-Aminobenzoic acid.......................................0.2mg Riboflavin ........................................................0.2mg FeCl3 ................................................................0.2mg Na2MoO4·4H2O ...............................................0.2mg KI .....................................................................0.1mg CuSO4·5H2O ..................................................0.04mg Folic acid ..........................................................2.0µg Biotin ................................................................2.0µg pH 4.5 ± 0.2 at 25°C
Preparation of Yeast Nitrogen Base: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly.
Chicken egg yolks..................................................66 Whole chicken egg...................................................6
Preparation of Medium: To 100.0mL of yeast nitrogen base, add 10.0g of carbohydrate. Mix thoroughly. Filter sterilize. Aseptically distribute 0.5mL into tubes containing 4.5mL of sterile, distilled/ deionized water.
Preparation of Egg Yolk Emulsion: Soak eggs
Use: For the cultivation and differentiation of bacte-
with 1:100 dilution of saturated mercuric chloride so-
ria based on carbohydrate assimilation.
Egg Yolk Emulsion: Composition:
476
Wickerham Broth
Wickerham Broth Composition per 100.0mL: KNO3 ................................................................0.78g Yeast carbon base........................................ 100.0mL pH 4.5 ± 0.2 at 25°C
Yeast Carbon Base: Composition per liter: Glucose .............................................................10.0g KH2PO4 ...............................................................1.0g MgSO4·7H2O ......................................................0.5g NaCl ....................................................................0.1g CaCl2·2H2O.........................................................0.1g DL-Methionine...................................................0.02g DL-Tryptophan...................................................0.02g L-Histidine·HCl .................................................0.01g Inositol .............................................................2.0mg H3BO3 ..............................................................0.5mg ZnSO4·7H2O ....................................................0.4mg MnSO4·4H2O ...................................................0.4mg Thiamine·HCl ..................................................0.4mg Pyridoxine........................................................0.4mg Niacin...............................................................0.4mg Calcium pantothenate ......................................0.4mg p-Aminobenzoic acid.......................................0.2mg Riboflavin ........................................................0.2mg FeCl3 ................................................................0.2mg Na2MoO4·4H2O ...............................................0.2mg KI .....................................................................0.1mg CuSO4·5H2O ..................................................0.04mg Folic acid.......................................................... 2.0µg Biotin ............................................................... 2.0µg
Preparation of Yeast Carbon Base: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly.
Preparation of Medium: To 100.0mL of yeast carbon base, add 0.78g of KNO3 (or peptone). Mix thoroughly. Filter sterilize. Aseptically distribute 0.5mL into tubes containing 4.5mL of sterile distilled/deionized water. Use: For the cultivation and differentiation of bacteria based on nitrate assimilation.
Wickerham Broth with Raffinose Composition per 100.0mL: Raffinose ...........................................................20.0g Yeast nitrogen base ..................................... 100.0mL
Yeast Nitrogen Base, 10X: Composition per liter: Glucose .............................................................10.0g KH2PO4 ...............................................................1.0g MgSO4·7H2O ......................................................0.5g NaCl ....................................................................0.1g CaCl2·2H2O.........................................................0.1g
DL-Methionine...................................................0.02g DL-Tryptophan...................................................0.02g L-Histidine·HCl .................................................0.01g
Inositol .............................................................2.0mg H3BO3 ..............................................................0.5mg ZnSO4·7H2O ....................................................0.4mg MnSO4·4H2O ...................................................0.4mg Thiamine·HCl ..................................................0.4mg Pyridoxine........................................................0.4mg Niacin...............................................................0.4mg Calcium pantothenate ......................................0.4mg p-Aminobenzoic acid.......................................0.2mg Riboflavin ........................................................0.2mg FeCl3 ................................................................0.2mg Na2MoO4·4H2O ...............................................0.2mg KI .....................................................................0.1mg CuSO4·5H2O ..................................................0.04mg Folic acid ..........................................................2.0µg Biotin ................................................................2.0µg pH 4.5 ± 0.2 at 25°C
Preparation of Yeast Nitrogen Base: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly.
Preparation of Medium: To 100.0mL of yeast nitrogen base, add 20.0g of raffinose. Mix thoroughly. Filter sterilize. Aseptically distribute 0.5mL into tubes containing 4.5mL of sterile distilled/deionized water.
Use: For the cultivation and differentiation of bacteria based on carbohydrate assimilation.
Wilkins-Chalgren Agar Composition per liter: Agar ..................................................................15.0g Gelatin peptone.................................................10.0g Pancreatic digest of casein................................10.0g NaCl....................................................................5.0g Yeast extract........................................................5.0g Glucose ...............................................................1.0g L-Arginine ...........................................................1.0g Sodium pyruvate.................................................1.0g Hemin ..............................................................5.0mg Vitamin K1 (Menadione) .................................0.5mg pH 7.1 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Add antibiotic to be assayed; varying concentrations of antibiotics are used. Mix thoroughly. Pour into sterile Petri dishes or leave in tubes.
Wilkins-Chalgren Anaerobe Agar with NS Supplement Use: For the cultivation and maintenance of anaero-
477
bic bacteria. For standardized antimicrobic susceptibility testing to determine the minimum inhibitory concentrations of antimicrobics for anaerobic bacteria.
Hemin ..............................................................5.0mg Sodium succinate .............................................2.5mg Vancomycin .....................................................2.5mg Menadione .......................................................0.5mg
Wilkins-Chalgren Anaerobe Agar
Preparation of GN Anaerobe Selective Supplement: Add components to distilled/deionized
Composition per liter: Agar ..................................................................10.0g Pancreatic digest of casein................................10.0g Gelatin peptone .................................................10.0g NaCl ....................................................................5.0g Yeast extract........................................................5.0g Glucose ...............................................................1.0g L-Arginine ...........................................................1.0g Sodium pyruvate .................................................1.0g Hemin...............................................................5.0mg Menadione .......................................................0.5mg Defibrinated blood ........................................ 50.0mL Tween 80......................................................... 1.0mL pH 7.1 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath.
water and bring volume to 20.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except defibrinated blood and GN anaerobe selective supplement, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Aseptically add 20.0mL of GN anaerobe selective supplement and 50.0mL of defibrinated blood. Bring volume to 1.0L with distilled/deionized water. Mix thoroughly. Pour into sterile Petri dishes or leave in tubes.
Use: For the selective isolation of Gram-negative anaerobes.
Preparation of Medium: Add components, except defibrinated blood, to distilled/deionized water and bring volume to 950.0mL. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure– 121°C. Cool to 50°–55°C. Aseptically add 50.0mL of defibrinated blood. Mix thoroughly. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation of nonsporulating anaerobes.
Wilkins-Chalgren Anaerobe Agar with GN Supplement Composition per liter: Agar ..................................................................10.0g Pancreatic digest of casein................................10.0g Gelatin peptone .................................................10.0g NaCl ....................................................................5.0g Yeast extract........................................................5.0g Glucose ...............................................................1.0g L-Arginine ...........................................................1.0g Sodium pyruvate .................................................1.0g Hemin...............................................................5.0mg Menadione .......................................................0.5mg Defibrinated blood ........................................ 50.0mL GN anaerobe selective supplement............... 20.0mL pH 7.1 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath. GN Anaerobe Selective Supplement Composition per 20.0mL: Nalidixic acid .................................................10.0mg
Wilkins-Chalgren Anaerobe Agar with NS Supplement Composition per liter: Agar ..................................................................10.0g Pancreatic digest of casein................................10.0g Gelatin peptone.................................................10.0g NaCl....................................................................5.0g Yeast extract........................................................5.0g Glucose ...............................................................1.0g L-Arginine ...........................................................1.0g Sodium pyruvate.................................................1.0g Hemin ..............................................................5.0mg Menadione .......................................................0.5mg Defibrinated blood ........................................ 50.0mL NS anaerobe selective supplement .............. 20.0 mL Tween 80......................................................... 1.0mL pH 7.1 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from Oxoid Unipath. NS Anaerobe Selective Supplement: Composition per 20.0mL: Sodium pyruvate.................................................1.0g Nalidixic acid....................................................0.01g Hemin ..............................................................5.0mg Menadione .......................................................0.5mg
Preparation of NS Anaerobe Selective Supplement: Add components to distilled/deionized water and bring volume to 20.0mL. Mix thoroughly. Filter sterilize.
478
Wilkins-Chalgren Anaerobe Broth
Preparation of Medium: Add components, except defibrinated blood and NS anaerobe selective supplement, to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°–55°C. Aseptically add 20.0mL of NS anaerobe selective supplement and 50.0mL of defibrinated blood. Bring volume to 1.0L with distilled/deionized water. Mix thoroughly. Pour into sterile Petri dishes or leave in tubes.
Use: For the selective isolation of nonsporulating anaerobes.
Wilkins-Chalgren Anaerobe Broth (Anaerobe Broth, MIC) Composition per liter: Pancreatic digest of casein................................10.0g Gelatin peptone .................................................10.0g NaCl ....................................................................5.0g Yeast extract........................................................5.0g Glucose ...............................................................1.0g L-Arginine ...........................................................1.0g Sodium pyruvate .................................................1.0g Hemin...............................................................5.0mg Menadione .......................................................0.5mg pH 7.1 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems and Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C.
Use: For the cultivation and antimicrobial susceptibility (MIC) testing of anaerobic bacteria.
Wilson Blair Base Composition per liter: Agar ..................................................................30.0g Proteose peptone no. 3 ......................................10.0g Glucose .............................................................10.0g Beef extract .........................................................5.0g NaCl ....................................................................5.0g Selective reagent ........................................... 70.0mL Brilliant Green (1% solution) ......................... 4.0mL pH 7.3 ± 0.2 at 25°C
Selective Reagent: Composition per 100.0mL: Solution 1.................................................... 100.0mL Solution 2.................................................... 100.0mL Solution 3.................................................... 100.0mL Solution 4...................................................... 20.2mL
Preparation of Selective Reagent: Combine 100.0mL of solution 1, 100.0mL of solution 2, 100.0mL of solution 3, and 20.2mL of solution 4. Mix thoroughly. Gently heat to boiling until a slategrey color develops. Cool to 50°C. Solution 1: Composition per 100.0mL: NaHSO3 ............................................................40.0g
Preparation of Solution 1: Add NaHSO3 to 100.0mL of distilled/deionized water. Mix thoroughly.
Solution 2: Composition per 100.0mL: NaH2PO4 ...........................................................21.0g
Preparation of Solution 2: Add NaH2PO4 to 100.0mL of distilled/deionized water. Mix thoroughly. Solution 3: Composition per 100.0mL: Bismuth ammonium citrate...............................12.5g
Preparation of Solution 3: Add bismuth ammonium citrate to 100.0mL of distilled/deionized water. Mix thoroughly.
Solution 4: Composition per 20.2mL: FeSO4 ................................................................0.96g
Preparation of Solution 4: Add FeSO4 to
20.0mL of distilled/deionized water. Add 0.2mL of concentrated HCl. Mix thoroughly.
Preparation of Medium: Add components, except selective reagent and Brilliant Green solution, to distilled/deionized water and bring volume to 976.0mL. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C. Aseptically add selective reagent and Brilliant Green solution. Mix thoroughly. Pour into sterile Petri dishes or leave in tubes.
Use: For the isolation and cultivation of Salmonella, especially Salmonella typhi.
Winge Agar Composition per liter: Glucose .............................................................20.0g Agar ..................................................................15.0g Yeast extract........................................................3.0g pH 7.2 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 7.2. Gently heat and bring to boiling. Distribute into tubes or flasks. Auto-
XL Agar Base clave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of Candida albicans and Candida tropicalis.
Wolin-Bevis Medium Composition per liter: Agar ..................................................................20.0g (NH4)2SO4...........................................................1.0g KH2HPO4 ............................................................1.0g Glucose .............................................................0.25g L-Histidine·HCl .................................................0.25g Tween 80 (polysorbate 80).............................. 3.0mL pH 5.4 ± 0.2 at 25°C
Preparation of Medium: Add components to
479
Preparation of Solution 1: Add components to distilled/deionized water and bring volume to 900.0mL. Mix thoroughly. Gently heat and bring to boiling.
Solution 2: Composition per 100.0mL: Xanthine..............................................................4.0g
Preparation of Solution 2: Add xanthine to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Gently heat and bring to boiling.
Preparation of Medium: Combine solutions 1 and 2. Mix thoroughly. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the differentiation of aerobic Actinomycete
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
species. Clearing around a colony indicates utilization of xanthine. Streptomyces species utilize xanthine; most Nocardia and Actinomadura species do not utilize xanthine.
Use: For the enhanced production of chlamy-
XL Agar Base (Xylose Lysine Agar Base)
dospores by Candida albicans.
Composition per liter:
Worfel-Ferguson Agar Composition per liter: Sucrose..............................................................20.0g Agar ..................................................................15.0g NaCl ....................................................................2.0g Yeast extract........................................................2.0g K2SO4..................................................................1.0g MgSO4·7H2O ....................................................0.25g pH 6.5 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the detection of capsule production by Klebsiella. For serological detection of the Neufeld (Quellung) reaction.
Xanthine Agar Composition per liter: Solution 1.................................................... 900.0mL Solution 2.................................................... 100.0mL pH 7.0 ± 0.2 at 25°C
Solution 1: Composition per 900.0mL: Agar ..................................................................15.0g Pancreatic digest of gelatin .................................5.0g Beef extract .........................................................3.0g
Agar ..................................................................13.5g Lactose................................................................7.5g Sucrose................................................................7.5g L-Lysine...............................................................5.0g NaCl....................................................................5.0g Xylose .................................................................3.5g Yeast extract........................................................3.0g Phenol Red........................................................0.08g Thiosulfate-citrate solution........................... 20.0mL pH 7.5 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems.
Thiosulfate-Citrate Solution: Composition per 100.0mL: Na2S2O3 ............................................................34.0g Ferric ammonium citrate.....................................4.0g
Preparation of Thiosulfate-Citrate Solution: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly.
Preparation of Medium: Add components, except thiosulfate-citrate solution, to distilled/deionized water and bring volume to 980.0mL. Mix thoroughly. Gently heat while stirring and bring to boiling. Distribute into tubes or flasks. Autoclave for 10 min at 14 psi pressure–118°C. Cool to 55°C. Aseptically add 20.0 mL of the sterile thiosulfate-citrate solution. Mix thoroughly. Pour into sterile Petri dishes or leave in tubes.
480
XL Agar Base
Use: For the isolation, cultivation, and differentiation of enteric pathogens. Nonfermenting xylose/lactose/sucrose bacteria appear as red colonies. Xylosefermenting, lysine-decarboxylating bacteria appear as red colonies. Xylose-fermenting, lysine-nondecarboxylating bacteria appear as opaque yellow colonies. Lactose or sucrose-fermenting bacteria appear as yellow colonies.
XL Agar Base Composition per liter: Agar ....................................................................15 g Lactose ................................................................7.5g Sucrose................................................................7.5g L-Lysine...............................................................5.0g NaCl ....................................................................5.0g Xylose ...............................................................3.75g Yeast extract........................................................3.0g Phenol Red........................................................0.08g Thiosulfate-citrate solution ........................... 20.0mL pH 7.4 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems. Thiosulfate-Citrate Solution: Composition per 100.0mL: Na2S2O3 ............................................................34.0g Ferric ammonium citrate.....................................4.0g
Preparation of Thiosulfate-Citrate Solution: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly.
Preparation of Medium: Add components, except thiosulfate-citrate solution, to distilled/deionized water and bring volume to 980.0mL. Mix thoroughly. Gently heat while stirring and bring to boiling. Distribute into tubes or flasks. Autoclave for 10 min at 14 psi pressure–118°C. Cool to 55°C. Aseptically add 20.0 mL of the sterile thiosulfate-citrate solution. Mix thoroughly. Pour into sterile Petri dishes or leave in tubes.
Use: For the isolation, cultivation, and differentiation of enteric pathogens. Nonfermenting xylose/lactose/sucrose bacteria appear as red colonies. Xylosefermenting, lysine-decarboxylating bacteria appear as red colonies. Xylose-fermenting, lysine-nondecarboxylating bacteria appear as opaque yellow colonies. Lactose or sucrose-fermenting bacteria appear as yellow colonies.
Lactose................................................................7.5g Sucrose................................................................7.5g Na2S2O3 ..............................................................6.8g L-Lysine...............................................................5.0g NaCl....................................................................5.0g Xylose .................................................................3.5g Yeast extract........................................................3.0g Sodium desoxycholate ........................................2.5g Ferric ammonium citrate.....................................0.8g Phenol Red........................................................0.08g pH 7.5 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems and Oxoid Unipath.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Do not overheat. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes. Plates should be poured as soon as possible to avoid precipitation.
Use: For the isolation and differentiation of enteric pathogens, especially Shigella and Providencia species. Nonfermenting xylose/lactose/sucrose bacteria appear as red colonies. Xylose-fermenting, lysinedecarboxylating bacteria appear as red colonies. Xylose-fermenting, lysine-nondecarboxylating bacteria appear as opaque yellow colonies. Lactose or sucrose-fermenting bacteria appear as yellow colonies.
Xylose Lactose Tergitol 4 (XLT-4) Composition per 1004.6mL: Agar ..................................................................18.0g Lactose................................................................7.5g Sucrose................................................................7.5g Na2S2O3 ..............................................................6.8g Lysine..................................................................5.0g NaCl....................................................................5.0g Xylose ...............................................................3.75g Yeast extract........................................................3.0g Proteose peptone.................................................1.6g Ferric ammonium citrate.....................................0.8g Phenol Red........................................................0.08g Selective supplement solution ........................ 4.6mL pH 7.4 ± 0.2 at 25°C
Source: This medium is available as a premixed
XLD Agar (Xylose Lysine Deoxycholate Agar) Composition per liter: Agar ..................................................................13.5g
powder from Oxoid Unipath.
Selective Supplement Solution: Composition per 100.0mL: Tergitol 4..................................................Proprietary
Y 1 Adrenal Cell Growth Medium Preparation of Selective Supplement Solution: Available as premixed solution.
Preparation of Medium: Add components, except selective supplement solution, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Add 4.6mL of selective supplement solution. Mix thoroughly. Gently heat while stirring and bring to boiling. Do not autoclave. Cool to 50°C. Mix thoroughly. Pour into sterile Petri dishes.
Use: For the isolation and identification of Salmonellae from clinical specimens.The presence of the selective agent, Tergitol 4, in this medium inhibits many organisms that can be problematic on other plating media. In addition, biochemical and pH changes within the medium allow Salmonella spp. (black colonies) to be differentiated from organisms, such as E. coli (yellow colonies) and Shigella spp. (red colonies). The enhanced selectivity of XLT-4 Agar reduces the need for further identification procedures, saving time and money, and results in fewer false presumptive positive colonies when compared to other Salmonella plating media.
Xylose Sodium Deoxycholate Citrate Agar Composition per liter: Agar ..................................................................12.0g Xylose ...............................................................10.0g Sodium citrate .....................................................5.0g Na2S2O3·5H2O ....................................................5.0g Beef extract .........................................................5.0g Peptone................................................................5.0g NaCl ....................................................................2.5g Sodium deoxycholate..........................................2.5g Ferric ammonium citrate.....................................1.0g Neutral Red (1% solution) .............................. 2.5mL pH 7.5 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling for 20 sec. Do not autoclave. Cool to 45°–50°C. Pour into sterile Petri dishes.
Use: For the cultivation of Salmonella species and some Shigella species.
Y 1 Adrenal Cell Growth Medium Composition per 101.0mL: Ham’s F-10 medium ..................................... 90.0mL Fetal bovine serum........................................ 10.0mL Penicillin-streptomycin solution ..................... 1.0mL pH 7.0 ± 0.2 at 25°C
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Ham’s F-10 Medium: Composition per liter: NaCl....................................................................7.4g NaHCO3..............................................................1.2g Glucose ...............................................................1.1g NaH2PO4·H2O...................................................0.29g KCl....................................................................0.28g L-Arginine·HCl..................................................0.21g L-Glutamine ......................................................0.15g MgSO4·7H2O ....................................................0.15g Sodium pyruvate............................................... 0.11g KH2PO4.............................................................0.08g CaCl2·2H2O ......................................................0.04g L-Cystine·2HCl .................................................0.04g L-Histidine·HCl·H2O.........................................0.02g L-Lysine·HCl .....................................................0.02g L-Asparagine-H2O.............................................0.01g L-Aspartic acid ..................................................0.01g L-Glutamic acid.................................................0.01g L-Leucine ..........................................................0.01g L-Proline............................................................0.01g L-Serine .............................................................0.01g L-Alanine..........................................................8.9mg Glycine.............................................................7.5mg D-Phenylalanine ...............................................5.0mg L-Methionine ....................................................4.5mg Hypoxanthine...................................................4.1mg L-Threonine ......................................................3.6mg L-Valine ........................................................... 3.5mg L-Isoleucine ......................................................2.6mg L-Tyrosine ........................................................1.8mg Vitamin B12 ......................................................1.4mg Folic acid .........................................................1.3mg Phenol Red.......................................................1.2mg Thiamine·HCl ..................................................1.0mg FeSO4·7H2O ....................................................0.8mg Choline chloride...............................................0.7mg D-Calcium pantothenate ...................................0.7mg Thymidine........................................................0.7mg Niacinamide.....................................................0.6mg L-Tryptophan....................................................0.6mg Isoinositol ........................................................0.5mg Riboflavin ........................................................0.4mg Lipoic acid .......................................................0.2mg Pyridoxine·HCl ................................................0.2mg ZnSO4·7H2O ..................................................0.03mg Biotin .............................................................0.02mg CuSO4·5H2O .....................................................3.0µg
Preparation of Ham’s F-10 Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly.
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Y 1 Adrenal Cell Growth Medium
Penicillin-Streptomycin Solution: Composition per 100.0mL: Streptomycin .......................................................0.5g Penicillin G ................................................500,000U
Preparation of Penicillin-Streptomycin Solution: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Aseptically combine components. Filter sterilize. Store at 4-5°C.
Use: For the cultivation of Y-1 mouse adrenal tissue culture cells used for the detection of heat-labile toxin (LT) produced by enterotoxigenic strains of Escherichia coli. LT causes the conversion of elongated fibroblastlike cells into round, refractile cells.
Y 1 Adrenal Cell Growth Medium Composition per 580.0mL: Ham’s F-10 medium ................................... 500.0mL Fetal bovine serum........................................ 75.0mL Penicillin-streptomycin solution ..................... 5.0mL pH 7.0 ± 0.2 at 25°C
Ham’s F-10 Medium: Composition per liter: NaCl ....................................................................7.4g NaHCO3 ..............................................................1.2g Glucose ...............................................................1.1g NaH2PO4·H2O...................................................0.29g KCl....................................................................0.28g L-Arginine·HCl..................................................0.21g L-Glutamine.......................................................0.15g MgSO4·7H2O ....................................................0.15g Sodium pyruvate ...............................................0.11g KH2PO4 .............................................................0.08g CaCl2·2H2O.......................................................0.04g L-Cystine·2HCl..................................................0.04g L-Histidine·HCl·H2O .........................................0.02g L-Lysine·HCl .....................................................0.02g L-Asparagine-H2O.............................................0.01g L-Aspartic acid ..................................................0.01g L-Glutamic acid .................................................0.01g L-Leucine...........................................................0.01g L-Proline ............................................................0.01g L-Serine .............................................................0.01g L-Alanine..........................................................8.9mg Glycine.............................................................7.5mg D-Phenylalanine ...............................................5.0mg L-Methionine ....................................................4.5mg Hypoxanthine...................................................4.1mg L-Threonine ......................................................3.6mg L-Valine ........................................................... 3.5mg L-Isoleucine ......................................................2.6mg L-Tyrosine.........................................................1.8mg
Vitamin B12 ......................................................1.4mg Folic acid .........................................................1.3mg Phenol Red.......................................................1.2mg Thiamine·HCl ..................................................1.0mg FeSO4·7H2O ....................................................0.8mg Choline chloride...............................................0.7mg D-Calcium pantothenate ...................................0.7mg Thymidine........................................................0.7mg Niacinamide.....................................................0.6mg L-Tryptophan....................................................0.6mg Isoinositol ........................................................0.5mg Riboflavin ........................................................0.4mg Lipoic acid .......................................................0.2mg Pyridoxine·HCl ................................................0.2mg ZnSO4·7H2O ..................................................0.03mg Biotin .............................................................0.02mg CuSO4·5H2O .....................................................3.0µg
Preparation of Ham’s F-10 Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly.
Penicillin-Streptomycin Solution: Composition per 100.0mL: Streptomycin.......................................................0.5g Penicillin G ................................................ 500,000U
Preparation of Penicillin-Streptomycin Solution: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation of Medium: Aseptically combine components. Filter sterilize. Store at 4°–5°C.
Use: For the cultivation of Y-1 mouse adrenal tissue culture cells used for the detection of cholera enterotoxin (CT) produced by enterotoxigenic strains of Vibrio cholerae or Vibrio mimicus. CT causes the conversion of elongated fibroblast-like cells into round, refractile cells.
Yeast Extract Agar Composition per liter: Agar ..................................................................15.0g Peptone ...............................................................9.5g Yeast extract........................................................7.0g Beef extract.........................................................5.0g NaCl....................................................................5.0g pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation of Aeromonas salmonicida.
Yeast Fermentation Medium
Yeast Extract Agar Composition per liter:
Use: For the isolation, cultivation, and maintenance of Propionibacterium species.
Agar ..................................................................20.0g Yeast extract........................................................1.0g Buffer solution ................................................ 2.0mL pH 6.0 ± 0.2 at 25°C
Buffer Solution: Composition per 400.0mL: KH2PO4 .............................................................60.0g Na2HPO4 ...........................................................40.0g
Preparation of Buffer Solution: Add 40.0g of Na2HPO4 to 300.0mL of distilled/deionized water. Mix thoroughly. Add 60.0g of KH2PO4. Mix thoroughly. Adjust pH to 6.0.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes.
Use: For the identification of Histoplasma capsulatum, Blastomyces dermatitidis, and Coccidioides immitis.
Yeast Extract Sucrose Agar (YESA) (ATCC Medium 2125) Composition per liter: Sucrose..............................................................20.0g Agar ..................................................................15.0g Yeast extract........................................................4.0g KH2PO4...............................................................1.0g MgSO4·7H2O ......................................................0.5g pH 6.2 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 6.2. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of various fungi.
Yeast Extract Agar Composition per liter: Agar ..................................................................15.0g Proteose peptone ...............................................10.0g NaCl ....................................................................5.0g Yeast extract........................................................3.0g
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation of a variety of heterotrophic microorganisms.
Yeast Extract Sodium Lactate Medium Composition per liter: Agar ..................................................................15.0g Pancreatic digest of casein................................10.0g Yeast extract......................................................10.0g Sodium lactate...................................................10.0g KH2PO4 ...............................................................2.5g MnSO4 .............................................................5.0mg pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
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Yeast Extract Sucrose Agar Composition per liter: Sucrose............................................................150.0g Agar ..................................................................20.0g Yeast extract......................................................20.0g MgSO4·7H2O ......................................................0.5g Trace metal solution........................................ 1.0mL pH 6.5 ± 0.2 at 25°C
Trace Metal Solution: Composition per 100.0mL: ZnSO4·7H2O .......................................................1.0g CuSO4·5H2O .......................................................0.5g
Preparation of Trace Metal Solution: Add components to 100.0mL distilled/deionized water. Mix thoroughly.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Adjust pH to 6.5. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of various fungi.
Yeast Fermentation Medium Composition per liter: Peptone ...............................................................7.5g Yeast extract........................................................4.5g
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Yeast Glucose Agar
Bromthymol Blue (1.6% solution).................. 1.0mL Carbohydrate solution..................................... 1.0mL
Moss Street, Liverpool and is available from health food shops worldwide.
Carbohydrate Solution: Composition per 10.0mL:
Preparation of Medium: Add components to
Carbohydrate.......................................................0.6g
Preparation of Carbohydrate Solution: Add carbohydrate to distilled/deionized water and bring volume to 10.0mL. Glucose, maltose, lactose, galactose, or trehalose may be used. If raffinose is used, prepare a 12% solution. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except carbohydrate solution, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute in 2.0mL volumes into test tubes that contain an inverted Durham tube. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 45°–50°C. Aseptically add 1.0mL of sterile carbohydrate solution. Mix thoroughly.
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation of Aeromonas salmonicida.
YEPD Medium Composition per liter: Agar ..................................................................20.0g Glucose .............................................................20.0g Peptone .............................................................20.0g Yeast extract......................................................10.0g
Preparation of Medium: Add components to
based on carbohydrate fermentation patterns. Yeasts that can ferment a specific carbohydrate turn the medium yellow.
distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Yeast Glucose Agar
Use: For the cultivation of a variety of heterotrophic microorganisms.
Use: For the cultivation and differentiation of yeast
Composition per liter: Agar ..................................................................15.0g Pancreatic digest of gelatin ...............................7.75g Beef extract .......................................................4.75g Yeast extract........................................................2.5g K2HPO4 ...............................................................2.5g Glucose ...............................................................1.0g pH 7.0 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation and maintenance of a wide variety of bacteria.
Yeastrel Agar Composition per liter: Agar ..................................................................15.0g Peptone................................................................9.5g Yeastrel................................................................7.0g Lab-lemco (meat extract)....................................5.0g NaCl ....................................................................5.0g pH 7.0 ± 0.2 at 25°C
Source: Lab-lemco is available from Oxoid Unipath. Yeastrel is produced by Mapleton’s Foods Ltd.,
Yersinia Selective Agar Base Composition per liter: Mannitol............................................................20.0g Peptone .............................................................17.0g Agar ..................................................................12.5g Proteose peptone.................................................3.0g Yeast extract........................................................2.0g Sodium pyruvate.................................................2.0g NaCl....................................................................1.0g Sodium desoxycholate ........................................0.5g MgSO4·7H2O ....................................................0.01g Neutral Red.......................................................0.03g Crystal Violet ...................................................1.0mg Selective supplement ...................................... 6.0mL pH 7.4 ± 0.2 at 25°C
Source: This medium is available as a premixed powder from BD Diagnostic Systems and Oxoid Unipath.
Selective Supplement: Composition per 6.0mL: Cefsulodin......................................................15.0mg Irgasan..............................................................4.0mg Novobiocin ......................................................2.5mg Ethanol............................................................ 2.0mL
YPNC Medium Preparation of Selective Supplement: Aseptically add components to 4.0mL of distilled/deionized water and 2.0mL of ethanol. Mix thoroughly.
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C. Aseptically add selective supplement. Mix thoroughly. Pour into sterile Petri dishes or leave in tubes.
Use: For the isolation and enumeration of Yersinia enterocolitica from clinical specimens.
YI-S Medium Composition per liter: YI broth....................................................... 880.0mL Bovine serum, heat inactivated................... 100.0mL Vitamin mixture 18 ...................................... 20.0mL
Source: Vitamin mixture 18 is available from Biofluids, Inc., Rockville, MD.
YI Broth: Composition per liter: YI base stock.............................................. 780.0mL 10× Glucose buffer stock ............................ 100.0mL
YI Base Stock: Composition per 780.0mL: Yeast extract......................................................30.0g L-Cysteine·HCl ...................................................1.0g NaCl ....................................................................1.0g Ascorbic acid ......................................................0.2g Ferric ammonium citrate..............................228.0mg
10× Glucose Buffer Stock: Composition per 100.0.0mL: Glucose .............................................................10.0g K2HPO4 ...............................................................1.0g KH2PO4 ...............................................................0.6g
Preparation of 10× Glucose Buffer Stock: Add components to distilled/deionized water and bring volume to 100.0mL. Mix thoroughly. Filter sterilize.
Preparation of YI Base Stock: Add components to 600.0mL of distilled/deionized water. Mix thoroughly. Bring volume to 780.0mL with distilled/ deionized water. Adjust pH to 6.8 with 1N NaOH. Distribute in 78.0mL aliquots to 100.0mL screwcapped bottles. Autoclave for 15 min at 15 psi pressure–121°C. Cool to room temperature.
485
cooled YI base stock. Adjust osmolarity with NaCl to 380.0milliosmols/kg.
Preparation of Medium: Aseptically add 2.0mL of vitamin mixture 18 and 10.0mL of heat-inactivated bovine serum to 88.0mL of YI broth. Distribute in 13.0mL aliquots to 16 x 125mm screw-capped test tubes. Store at 4°C in the dark with the caps screwed on tightly. Use within 96h.
Use: For the cultivation of Entamoeba species.
YPC Medium Composition per liter: Agar ..................................................................15.0g Proteose peptone...............................................15.0g Yeast extract........................................................5.0g KH2PO4...............................................................4.0g Sucrose................................................................2.5g Glucose ...............................................................2.0g L-Cystine .............................................................0.5g Na2SO3 ................................................................0.2g pH 7.2 ± 0.2 at 25°C
Preparation of Medium: Add components to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Gently heat and bring to boiling. Distribute into tubes or flasks. Autoclave for 15 min at 15 psi pressure–121°C. Pour into sterile Petri dishes or leave in tubes.
Use: For the cultivation of Pasteurella multocida.
YPNC Medium Composition per liter: Agar ..................................................................18.0g NaCl..................................................................2.92g KH2PO4...........................................................0.596g Yeast extract........................................................0.5g Sodium hydrogen glutamate (pH 6.0) ..............0.37g K2HPO4...........................................................0.107g NH4Cl .............................................................0.107g MgSO4·7H2O ..................................................0.049g Glucose solution ........................................... 10.0mL Trace metals solution ...................................... 1.0mL pH 6.0 ± 0.2 at 25°C
Glucose Solution: Composition per 10.0mL: Glucose ...............................................................4.0g
Preparation of Glucose Solution: Add glucose to distilled/deionized water and bring volume to 10.0mL. Mix thoroughly. Filter sterilize.
Preparation of YI Broth: Aseptically add
Trace Metals Solution: Composition per liter:
10.0mL of 10× glucose buffer stock to 78.0mL of
EDTA ................................................................50.0g
486
YPNC Medium
ZnSO4·7H2O .....................................................22.0g CaCl2 .................................................................5.54g MnCl2·4H2O .....................................................5.06g FeSO4·7H2O......................................................4.99g (NH4)6 Mo7O14·H2O .........................................1.10g CoSO4·5H2O .....................................................1.57g CoCl2·6H2O ......................................................1.61g
Preparation of Trace Metals Solution: Add components, one at a time, to distilled/deionized water and bring volume to 1.0L. Mix thoroughly. Filter sterilize.
Preparation of Medium: Add components, except glucose solution and trace metals solution, to distilled/deionized water and bring volume to 989.0mL. Mix thoroughly. Gently heat and bring to boiling. Adjust pH to 6.0 with KOH. Autoclave for 15 min at 15 psi pressure–121°C. Cool to 50°C. Aseptically add 10.0mL of sterile glucose solution and 1.0mL of sterile trace metals solution. Mix thoroughly. Pour into sterile Petri dishes or aseptically distribute into sterile tubes.
Use: For the cultivation and maintenance of a variety of Cryptococcus species.
Appendix
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Agars
Peptones
Below are some agars used as solidifying agents in various media.
Below is a list of some of the peptones that are used as ingredients in various media.
Agar Bacteriological (Agar No. 1) An agar with low calcium and magnesium. Available from Oxoid Unipath.
Acidase™ Peptone A hydrochloric acid hydrolysate of casein. It has a nitrogen content of 8% and is deficient in cystine and tryptophan. Available from BD Diagnostic Systems. Bacto Casitone A pancreatic digest of casein. Available from Difco, BD Diagnostic Systems. Bacto Peptamin A peptic digest of animal tissues. Available from Difco, BD Diagnostic Systems. Bacto Peptone An enzymatic digest of animal tissues. It has a high concentration of low molecular weight peptones and amino acids. Available from Difco, BD Diagnostic Systems. Bacto Proteose Peptone An enzymatic digest of animal tissues. It has a high concentration of high molecular weight peptones. Available from Difco, BD Diagnostic Systems. Bacto Soytone A enzymatic hydrolysate of soybean meal. Available from Difco, BD Diagnostic Systems. Bacto Tryptone A pancreatic digest of casein. Available from Difco, BD Diagnostic Systems. Bacto Tryptose An enzymatic hydrolysate containing numerous peptides including those of higher molecular weights. Available from Difco, BD Diagnostic Systems. Biosate™ Peptone A hydrolysate of plant and animal proteins. Available from BD Diagnostic Systems. Casein Hydrolysate A hydrolysate of casein prepared with hydrochloric acid digestion under pressure and neutralized with sodium hydroxide. It contains total nitrogen of 7.6% and NaCl of 28.3%. Available from Oxoid Unipath. Gelatone A pancreatic digest of gelatin. Available from Difco, BD Diagnostic Systems. Gelysate™ Peptone A pancreatic digest of gelatin deficient in cystine and tryptophan and which has a low carbohydrate content. Available from Oxoid Unipath.
Agar, Bacto A purified agar with reduced pigmented compounds, salts, and extraneous matter. Available from Difco, BD Diagnostic Systems. Agar, BiTek™ Agar prepared as a special technical grade. Available from Difco, BD Diagnostic Systems. Agar, Flake A technical grade agar. Available from Difco, BD Diagnostic Systems. Agar, Grade A A select grade agar containing minerals. Available from BD Diagnostic Systems. Agar, Granulated A high grade granulated agar that has been filtered, decolorized, and purified. Available from BD Diagnostic Systems. Agarose A low sulfate neutral gelling fraction of agar that is a complex galactose polysaccharide of near neutral charge. Agar, Purified A very high grade agar that has been filtered, decolorized, and purified by washing and extraction of refined agars. It has reduced mineral content. Available from BD Diagnostic Systems. Agar Technical (Agar No. 3) A technical grade agar. Available from Difco, BD Diagnostic Systems, and Oxoid Unipath. Ionagar A purified agar. Available from Oxoid Unipath. Noble Agar An agar that has been extensively washed and is essentially free of impurities. Available from Difco, BD Diagnostic Systems. Purified Agar An agar that has been extensively washed and extracted with water and organic solvent. Available from Difco, BD Diagnostic Systems, and Oxoid Unipath.
488
Meat and Plant Extracts
Lactoalbumin Hydrolysate A pancreatic digest of lactoalbumin, a milk whey protein. It has high levels of amino acids. It contains total nitrogen of 11.9% and NaCl of 1.4%. Available from Difco, BD Diagnostic Systems, and Oxoid Unipath. Liver Digest Neutralized A papaic digest of liver that contains total nitrogen of 11.0% and NaCl of 1.6%. Available from Oxoid Unipath. Mycological Peptone A peptone that contains total nitrogen of 9.5% and NaCl of 1.1%. Available from Oxoid Unipath. Myosate™ Peptone A pancreatic digest of heart muscle. Available from BD Diagnostic Systems. Neopeptone An enzymatic digest of protein. Available from Difco, BD Diagnostic Systems. Peptone Bacteriological Neutralized A mixed pancreatic and papaic digest of animal tissues. It contains total nitrogen of 14.0% and NaCl of 1.6%. Available from Difco, BD Diagnostic Systems, and Oxoid Unipath. Peptone P A peptic digest of fresh meat that has a high sulfur content and contains total nitrogen of 11.12% and NaCl of 9.3%. Available from Difco, BD Diagnostic Systems, and Oxoid Unipath. Peptonized Milk A pancreatic digest of high grade skim milk powder. It has a high carbohydrate and calcium concentration. It contains total nitrogen of 5.3% and NaCl of 1.6%. Available from Oxoid Unipath. Phytone™ Peptone A papaic digest of soybean meal. It has a high vitamin and a high carbohydrate content. Available from BD Diagnostic Systems. Polypeptone™ Peptone A mixture of peptones composed of equal parts of pancreatic digest of casein and peptic digest of animal tissue. Available from BD Diagnostic Systems. Proteose Peptone A specialized peptone prepared from a mixture of peptones that contains a wide variety of high molecular weight peptides. It contains total nitrogen of 12.7% and NaCl of 8.0%. Available from Difco, BD Diagnostic Systems, and Oxoid Unipath.
Proteose Peptone No. 2 An enzymatic digest of animal tissues with a high concentration of high molecular weight peptones. Available from Difco, BD Diagnostic Systems. Proteose Peptone No. 3 An enzymatic digest of animal tissues. It has a high concentration of high molecular weight peptones. Available from Difco, BD Diagnostic Systems. Soya Peptone A papaic digest of soybean meal with a high carbohydrate concentration. It contains total nitrogen of 8.7% and NaCl of 0.4%. Available from Oxoid Unipath. Soytone A papaic digest of soybean meal. Available from Difco, BD Diagnostic Systems, and Oxoid Unipath. Special Peptone A mixture of peptones, including meat, plant and yeast digests. It contains a wide variety of peptides, nucleotides, and minerals. It contains total nitrogen of 11.7% and NaCl of 3.5%. Available from Oxoid Unipath. Thiotone™ E Peptone An enzymatic digest of animal tissue. Available from BD Diagnostic Systems. Trypticase™ Peptone A pancreatic digest of casein. It has a very low carbohydrate content and a relatively high tryptophan content. Available from BD Diagnostic Systems. Tryptone A pancreatic digest of casein. It contains total nitrogen of 12.7% and NaCl of 0.4%. Available from Oxoid Unipath. Tryptone T A pancreatic digest of casein with lower levels of calcium, magnesium, and iron than tryptone. It contains total nitrogen of 11.7% and NaCl of 4.9%. Available from Difco, BD Diagnostic Systems, and Oxoid Unipath. Tryptose An enzymatic hydrolysate containing high molecular weight peptides. It contains total nitrogen of 12.2% and NaCl of 5.7%. Available from Difco, BD Diagnostic Systems, and Oxoid Unipath.
Meat and Plant Extracts Below is a list of some of the meat and plant extracts that are used as ingredients in various media.
Growth Factors Bacto Beef A desiccated powder of lean beef. Available from Difco, BD Diagnostic Systems. Bacto Beef Extract An extract of beef (paste). Available from Difco, BD Diagnostic Systems. Bacto Beef Extract Desiccated An extract of desiccated beef. Available from Difco, BD Diagnostic Systems. Bacto Beef Heart for Infusion A desiccated powder of beef heart. Available from Difco, BD Diagnostic Systems. Bacto Liver A desiccated powder of beef liver. Available from Difco, BD Diagnostic Systems. Lab-Lemco A meat extract powder. Available from Oxoid Unipath. Liver Desiccated Dehydrated ox livers. Available from Oxoid Unipath. Malt Extract A water soluble extract from germinated grain dried by low temperature evaporation. It has a high carbohydrate content. It contains total nitrogen of 1.1% and NaCl of 0.1%.
Growth Factors Many microorganisms have specific growth factor requirements that must be included in media for their successful cultivation. Vitamins, amino acids, fatty acids, trace metals, and blood components often must be added to media. Most often mixtures of growth factors are used in microbiological media. Acid hydrolysates of casein commonly are used as sources of amino acids. Extracts of yeast cells also are employed as sources of amino acids and vitamins for the cultivation of microorganisms. Many media, particularly those employed in the clinical laboratory, contain blood or blood components that serve as essential nutrients for fastidious microorganisms. X factor (heme) and V factor (nicotinamide adenine dinucleotide) often are supplied by adding hemoglobin (BBL and Difco, BD Diagnostic Systems), IsoVitaleX (BD Diagnostic Systems), and Supplement VX (Difco, BD Diagnostic Systems). Below is a list of some of the growth factors that are used as ingredients in microbiological media. Bacto Casamino Acids A mixture of amino acids formed by acid hydrolysis of casein. Available from Difco, BD Diagnostic Systems.
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Bacto Vitamin Free Casamino Acids A mixture of amino acids formed by acid hydrolysis of casein that is free of vitamins. Available from Difco, BD Diagnostic Systems. Bovine Albumin Bovine albumin fraction V 0.2% in 0.85% saline solution. Available from BD Diagnostic Systems. Bovine Blood, Citrated Calf blood washed and treated with sodium citrate as an anticoagulant. Available from BD Diagnostic Systems. Bovine Blood, Defibrinated Calf blood treated to denature fibrinogen without causing cell lysis. Available from BD Diagnostic Systems. Campylobacter Growth Supplement Sodium pyruvate, sodium metabisulfite, and FeSO4. Castenholtz Salts Agar, NaNO3, Na2HPO4, KNO3, nitrilotriacetic acid, MgSO4·7H2O, CaSO4·2H2O, NaCl, FeCl3, MnSO4, H3BO3, ZnSO4, CoCl2·6H2O, Na2MoO4, CuSO4, and H2SO4. CVA Enrichment Glucose, L-cysteine·HCl·H2O, vitamin B12, L-glutamine, L-cystine·2HCl, adenine, nicotinamide adenine dinucleotide, cocarboxylase, guanine·HCl, Fe(NO3)3, p-aminobenzoic acid, and thiamine·HCl. Cysteine Sulfide Reducing Agent L-Cysteine·HCl·H2O and Na2S·9H2O. Dubos Medium Albumin Albumin fraction V, glucose, and saline solution. Available from Difco, BD Diagnostic Systems. Dubos Oleic Albumin Complex Alkalinized oleic acid, albumin fraction V, and saline solution. Available from Difco, BD Diagnostic Systems. Egg Yolk Emulsion Chicken egg yolks and whole chicken egg. Available from Difco, BD Diagnostic Systems, and Oxoid Unipath. Egg Yolk Emulsion, 50% Chicken egg yolks, whole chicken egg, and saline solution. Available from Difco, BD Diagnostic Systems. EY Tellurite Enrichment Egg yolk suspension with potassium tellu-
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Growth Factors
rite. Available from Difco, BD Diagnostic Systems and Oxoid Unipath. Fresh Yeast Extract Solution Live, pressed, starch-free, Baker’s yeast.
hydrolyzed
tine, adenine, nicotinamide adenine dinucleotide, vitamin B12, thiamine pyrophosphate, guanine·HCl, Fe(NO3)3·6H2O, p-aminobenzoic acid, and thiamine·HCl. Available from BD Diagnostic Systems.
Fildes Enrichment A peptic digest of sheep or horse blood that is a rich source of growth factors including hemin and nicotinamide adenine dinucleotide. Available from BD Diagnostic Systems and Oxoid Unipath. Hemin Solution Hemin and NaOH.
Legionella Agar Enrichment L-Cysteine and ferric pyrophosphate. Available from Difco, BD Diagnostic Systems.
Hemoglobin Dried bovine hemoglobin. Used to provide hemin required by many fastidious microorganisms. Available from BD Diagnostic Systems. Hemoglobin Solution 2% Provides hemin required by many fastidious microorganisms. Available from BD Diagnostic Systems. Hoagland Trace Element Solution, Modified H3BO3, MnCl2·4H2O, AlCl3, CoCl2, CuCl2, KI, NiCl2, ZnCl2, BaCl2, Na2MoO4, SeCl4, SnCl2·2H2O, NaVO3·H2O, KBr, and LiCl.
Leptospira Enrichment Lyophilized pooled rabbit serum containing hemoglobin that provides long chain fatty acids and B vitamins for growth of Leptospira species. Available from Diagnostic Systems.
Horse Blood, Citrated Horse blood washed and treated with sodium citrate used as an anticoagulant. Available from BD Diagnostic Systems. Horse Blood, Defibrinated Horse blood treated to denature fibrinogen without causing cell lysis. Available from BD Diagnostic Systems and Oxoid Unipath. Horse Blood, Hemolysed Horse blood treated to lyse cells. Available from Oxoid Unipath. Horse Blood, Oxalated Horse blood treated with potassium oxalate as an anticoagulant. Available from Oxoid Unipath. Horse Serum Horse blood is allowed to clot at 2°–8°C so that the serum separates; the serum is filter sterilized. Serum usually is inactivated by heating to 56°C for 30 min to eliminate lipases that would cause degradation of lipids and inactivation of complement. Available from Difco, BD Diagnostic Systems, and Oxoid Unipath. IsoVitaleX® Enrichment Glucose, L-cysteine·HCl,
L-glutamine, L-cys-
Legionella BCYE Growth Supplement ACES buffer/KOH, ferric pyrophosphate, Lcysteine-HCl, and α-ketoglutarate. For the enrichment of Legionella species. Available from Oxoid Unipath.
Middlebrook ADC Enrichment NaCl, bovine albumin fraction V, glucose, and catalase. The albumin binds free fatty acids that may be toxic to mycobacteria. Available from BD Diagnostic Systems. Middlebrook OADC Enrichment NaCl, bovine albumin, glucose, oleic acid, and catalase. The albumin binds free fatty acids that may be toxic to mycobacteria; the enrichment provides oleic acid used by Mycobacterium tuberculosis for growth. Available from BD Diagnostic Systems. Mycoplasma Enrichment without Penicillin Horse serum, fresh autolysate of yeast— yeast extract, and thallium acetate. Provides cholesterol and nucleic acids for growth of Mycoplasma species. The thallium selectively inhibits other microorganisms. Available from BD Diagnostic Systems. Mycoplasma Supplement Yeast extract and horse serum. Available from Difco, BD Diagnostic Systems. Nitsch’s Trace Elements MnSO4, H3BO3, ZnSO4, Na2MoO4, CuSO4, CoCl2·6H2O, and H2SO4. Oleic Albumin Complex NaCl, bovine albumin fraction V, and oleic acid. The albumin binds free fatty acids that may be toxic to mycobacteria and the enrichment provides oleic acid that is used by Mycobacterium tuberculosis for growth. Available from BD Diagnostic Systems.
Selective Components PPLO Serum Fraction Serum fraction A. Available from Difco, BD Diagnostic Systems. Rabbit Blood, Citrated Rabbit blood washed and treated with sodium citrate as an anticoagulant. Available from BD Diagnostic Systems. Rabbit Blood, Defibrinated Rabbit blood treated to denature fibrinogen without causing cell lysis. Available from BD Diagnostic Systems. RPF Supplement Fibrinogen, rabbit plasma, trypsin inhibitor, and potassium tellurite. For the selection and nutrient supplementation of Staphylococcus aureus. Available from Oxoid Unipath. Sheep Blood, Citrated Sheep blood washed and treated with sodium citrate as an anticoagulant. Available from BD Diagnostic Systems. Sheep Blood, Defibrinated Sheep blood treated to denature fibrinogen without causing cell lysis. Available from Oxoid Unipath. SLA Trace Elements FeCl2·4H2O, H3BO3, CoCl2·6H2O, ZnCl2, MnCl2·4H2O, NiCl2·6H2O, CuCl2·2H2O, Na2MoO4·2H2O, and Na2SeO3·5H2O. Soil Extract African Violet soil and Na2CO3. Supplement A Yeast concentrate with Crystal Violet. Available from Difco, BD Diagnostic Systems. Supplement B Yeast concentrate, glutamine, coenzyme, cocarboxylase, hematin, and growth factors. Available from Difco, BD Diagnostic Systems. Supplement C Yeast concentrate. Available from Difco, BD Diagnostic Systems. Supplement VX Essential growth factors V and X. Available from Difco, BD Diagnostic Systems. VA Vitamin Solution Nicotinamide, thiamine·HCl, p-aminobenzoic acid, biotin, calcium pantothenate, pyridoxine·2HCl, and cyanocobalamin. Vitamin K1 Solution Vitamin K1 and ethanol.
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Vitox Supplement Glucose, L-cysteine·HCl, L-glutamine, L-cystine, adenine sulfate, nicotinamide adenine dinucleotide, cocarboxylase, guanine·HCl, Fe(NO3)3·6H2O, p-aminobenzoic acid, vitamin B12, and thiamine·HCl. Available from Oxoid Unipath. Yeast Autolysate Growth Supplement Yeast autolysate fractions, glucose, and NaHCO3. Available from Oxoid Unipath. Yeast Extract A water soluble extract of autolyzed yeast cells. Available from BD Diagnostic Systems, and Oxoid Unipath. Yeastolate A water soluble fraction of autolyzed yeast cells rich in vitamin B complex. Available from Difco, BD Diagnostic Systems.
Selective Components Below is a list of selective components that are used to inhibit the growth of nontarget microorganisms and favor the growth of specific organisms. Selective media are especially useful in the isolation of specific microorganisms from mixed populations. Ampicillin Selective Supplement Ampicillin. Used in media for the selection of Aeromonas hydrophila. Available from Oxoid Unipath. Anaerobe Selective Supplement GN Hemin, menadione, sodium succinate, nalidixic acid, and vancomycin. For the selection of Gram-negative anaerobes. Available from Oxoid Unipath. Anaerobe Selective Supplement NS Hemin, menadione, sodium pyruvate, and nalidixic acid. For the selection of nonsporulating anaerobes. Available from Oxoid Unipath. Bacillus cereus Selective Supplement Polymyxin B. For the selection of Bacillus cereus. Available from Oxoid Unipath. Bordetella Selective Supplement Cephalexin. For the selection of Bordetella species. Available from Oxoid Unipath. Brucella Selective Supplement Polymyxin B, bacitracin, cycloheximide, nalidixic acid, nystatin, and vancomycin. For the selection of Brucella species. Available from Oxoid Unipath. Campylobacter Selective Supplement Blaser-Wang Vancomycin, polymyxin B, trimethoprim, amphotericin B, cephalothin. For the selec-
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Selective Components
tion of Campylobacter species. Available from Oxoid Unipath. Campylobacter Selective Supplement Butzler Bacitracin, cycloheximide, colistin sulfate, sodium cephazolin, and novobiocin. For the selection of Campylobacter species. Available from Oxoid Unipath. Campylobacter Selective Supplement Preston Polymyxin B, rifampicin, trimethoprim, and cycloheximide. For the selection of Campylobacter species. Available from Oxoid Unipath. Campylobacter Selective Supplement Skirrow Vancomycin, trimethoprim, and polymyxin B. For the selection of Campylobacter species. Available from Oxoid Unipath. CCDA Selective Supplement Cefoperazone and amphotericin B. For the selection of Campylobacter species. Available from Oxoid Unipath. Cefoperazone Selective Supplement Cefoperazone. For the selection of Campylobacter species. Available from Oxoid Unipath. CFC Selective Supplement Cetrimide, fucidin, and cephaloridine. For the selection of pseudomonads. Available from Oxoid Unipath. Chapman Tellurite Solution Potassium tellurite 1% solution. Available from Difco, BD Diagnostic Systems. Chloramphenicol Selective Supplement Chloramphenicol. For the selection of yeasts and filamentous fungi. Available from Oxoid Unipath. Clostridium difficile Selective Supplement D-Cycloserine and cefoxitin. For the selection of Clostridium difficile. Available from Difco, BD Diagnostic Systems, and Oxoid Unipath. CN Inhibitor Cesulodin and novobiocin. It inhibits enteric Gram-negative microorganisms. Available from BD Diagnostic Systems. CNV Antimicrobic Colistin sulfate, nystatin, and vancomycin. Available from Difco, BD Diagnostic Systems. CNVT Antimicrobic Colistin sulfate, nystatin, vancomycin, and trimethoprim lactate. Available from Difco, BD Diagnostic Systems. Colbeck’s Egg Broth Egg emulsion and saline solution. Formerly
available from Difco, BD Diagnostic Systems—replaced with egg emulsion. Fraser Supplement Ferric ammonium sulfate, nalidixic acid, and Acriflavin hydrochloride. For the selection of Listeria species. Available from Oxoid Unipath. Gardnerella vaginalis Selective Supplement Gentamicin sulfate, nalidixic acid, and amphotericin B. For the selection of Gardnerella vaginalis. Available from Oxoid Unipath. GC Selective Supplement Yeast autolysate, glucose, Na2HCO3, vancomycin, colistin methane sulfonate, nystatin, and trimethoprim. For the selection of Neisseria species. Available from Oxoid Unipath. Helicobacter pylori Selective Supplement Dent Vancomycin, trimethoprim, cefulodin, and amphotericin B. For the selection of Helicobacter pylori. Kanamycin Sulfate Selective Supplement Kanamycin sulfate. For the selection of enterococci. Available from Oxoid Unipath. LCAT Selective Supplement Lincomycin, colistin sulfate, amphotericin B, and trimethoprim. For the selection of Neisseria species. Available from Oxoid Unipath. Legionella BMPA Selective Supplement Cefamandole, polymyxin B, and anisomycin. For the selection of Legionella species. Available from Oxoid Unipath. Legionella GVPC Selective Supplement Glycine, vancomycin hydrochloride, polymixin B sulfate, and cycloheximide. For the selection of Legionella species. Available from Oxoid Unipath. Legionella MWY Selective Supplement Glycine, polymyxin B, anisomycin, vancomycin, Bromthymol B, and Bromcresol Purple. For the selection of Legionella species. Available from Oxoid Unipath. Listeria Primary Selective Enrichment Supplement Nalidixic acid and acriflavin. For the selection of Listeria species. Available from Oxoid Unipath. Listeria Selective Enrichment Supplement Nalidixic acid, cycloheximide, and acriflavin. For the selection of Listeria species. Available from Oxoid Unipath. Listeria Selective Supplement MOX Colistin and moxalactam. For the selection
Selective Components of Listeria monocytogenes. Available from Oxoid Unipath. Listeria Selective Supplement Oxford Cycloheximide, colistin sulfate, acriflavin, cefotetan, and fosfomycin. For the selection of Listeria species. Available from Oxoid Unipath. Modified Oxford Antimicrobic Supplement Moxalactam and colistin sulfate. Available from Difco, BD Diagnostic Systems. MSRV Selective Supplement Novobiocin. For the selection of Salmonella. Available from Oxoid Unipath. Mycoplasma Supplement G Horse serum, yeast extract, thallous acetate, and penicillin. For the selection of Mycoplasma species. Available from Oxoid Unipath. Mycoplasma Supplement P Horse serum, yeast extract, thallous acetate, glucose, Phenol Red, Methylene Blue, penicillin, and Mycoplasma broth base. For the selection of Mycoplasma species. Available from Oxoid Unipath. Mycoplasma Supplement S Yeast extract, horse serum, thallium acetate, and penicillin. Available from Difco, BD Diagnostic Systems. Oxford Antimicrobic Supplement Cycloheximide, colistin sulfate, acriflavin, cefotetan, and fosfomycin. Available from Difco, BD Diagnostic Systems. Oxgall Dehydrated fresh bile. For the selection of bile tolerant bacteria. Available from Difco, BD Diagnostic Systems. Oxytetracycline GYE Supplement Oxytetracycline in a buffer. For the selection of yeasts and filamentous fungi. Available from Oxoid Unipath. PALCAM Selective Supplement Polymyxin B, acriflavin hydrochloride, and ceftazidime. For the selection of Listeria monocytogenes. Available from Oxoid Unipath. Perfringens OPSP Selective Supplement A Sodium sulfadiazine. For the selection of Clostridium perfringens. Available from Oxoid Unipath. Perfringens SFP Selective Supplement A Kanamycin sulfate and polymyxin B. For the selection of Clostridium perfringens. Available from Oxoid Unipath.
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Perfringens TSC Selective Supplement A D-Cycloserine. For the selection of Clostridium perfringens. Available from Oxoid Unipath. Sodium Desoxycholate Sodium salt of desoxycholic acid. Available from Difco, BD Diagnostic Systems. Sodium Taurocholate Sodium salt of conjugated bile acid—75% sodium taurocholate and 25% bile salts. For the selection of bile tolerant bacteria. Available from Difco, BD Diagnostic Systems. STAA Selective Supplement Streptomycin sulfate, cycloheximide, and thallous acetate. For the selection of Brochothrix thermosphacta. Available from Oxoid Unipath. Staph/Strep Selective Supplement Nalidixic acid and colistin sulfate. For the selection of Staphylococcus species and Streptococcus species. Available from Oxoid Unipath. Streptococcus Selective Supplement COA Colistin sulfate and oxolinic acid. For the selection of Streptococcus species. Available from Oxoid Unipath. Sulfamandelate Supplement Sodium sulfacetamide and sodium mandelate. For the selection of Salmonella species. Available from Oxoid Unipath. Tellurite Solution A solution containing potassium tellurite. Inhibits Gram-negative and most Gram-positive microorganisms. It is used for the isolation of Corynebacterium species, Streptococcus species, Listeria species, and Candida albicans. Available from BD Diagnostic Systems. Tinsdale Supplement Serum, potassium tellurite, and sodium thiosulfate. For the selection of Corynebacterium diphtheriae. Available from Oxoid Unipath. V C A Inhibitor Vancomycin, colistin, anisomycin, and trimethoprim. Inhibits most Gram-negative and Gram-positive bacteria and yeasts. It is used for the isolation of Neisseria species. Available from BD Diagnostic Systems. V C A T Inhibitor Vancomycin, colistin, anisomycin, and trimethoprim lactate. Inhibits most Gram-negative and Gram-positive bacteria and yeasts.
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pH Buffers
It is used for the isolation of Neisseria species. Available from BD Diagnostic Systems and Oxoid Unipath. V C N Inhibitor Colistin, vancomycin, and nystatin. Inhibits most Gram-negative and Gram-positive bacteria and yeasts. It is used for the isolation of Neisseria species. Available from BD Diagnostic Systems and Oxoid Unipath. V C N T Inhibitor Colistin, vancomycin, nystatin, and trimethoprim lactate. Inhibits most Gram-negative and Gram-positive bacteria and yeasts. It is used for the isolation of Neisseria species. Available from BD Diagnostic Systems and Oxoid Unipath. Yersinia Selective Supplement Cefsulodin, irgasan, and novobiocin. For the selection of Yersinia enterocolitica. Available from Oxoid Unipath.
pH Buffers . The pH using phosphate buffers is established by using varying volumes of equimolar concentrations of Na2HPO4 and NaH2PO4.
pH.
Na2HPO4 (mL)
5.4 5.6 5.8 6.0 6.2 6.4 6.6 6.8 7.0 7.2 7.4 7.6 7.8 8.0
NaH2PO4 (mL)
3.0 5.0 7.8 12.0 18.5 26.5 37.5 50.0 61.1 71.5 80.4 86.8 91.4 94.5
97.0 95.0 92.2 88.0 81.5 73.5 62.5 50.0 38.9 28.5 19.6 13.2 8.6 5.5
Differential Components Below is a list of some commonly used pH indicators and their color reactions.
pH Indicator
pH Range
m-Cresol Purple 0.5–2.5 Thymol Blue 1.2–2.8 Bromphenol Blue 3.0–4.6 Bromcresol 3.8–5.4 Green Chlorcresol 4.0–5.6 Green
Acid Color
Alkaline Color
Red Red Yellow Yellow
Yellow Yellow Blue Blue
Yellow
Blue
Methyl Red
4.2–6.3
Red
Yellow
pH Indicator
pH Range
Acid Color
Alkaline Color
Yellow Yellow
Red Purple
Yellow Yellow Yellow Yellow Yellow Colorless Colorless
Blue Red Red Purple Blue Red Red
Chlorphenol Red 5.0–6.6 Bromcresol 5.2–6.8 Purple Bromthymol Blue6.0–7.6 Phenol Red 6.8–8.4 Cresol Red 7.2–8.8 m-Cresol Purple 7.4–9.0 Thymol Blue 8.0–9.6 Cresolphthalein 8.2–9.8 Phenolphthalein 8.3–10.0
Preparation of Media The ingredients in a medium are usually dissolved and the medium is then sterilized. When agar is used as a solidifying agent the medium must be heated gently, usually to boiling, to dissolve the agar. In some cases where interactions of components, such as metals, would cause precipitates, solutions must be prepared and occasionally sterilized separately before mixing the various solutions to prepare the complete medium. The pH often is adjusted prior to sterilization, but in some cases sterile acid or base is used to adjust the pH of the medium following sterilization. Many media are sterilized by exposure to elevated temperatures. The most common method is to autoclave the medium. Different sterilization procedures are employed when heat-labile compounds are included in the formulation of the medium.
Autoclaving Autoclaving uses exposure to steam, generally under pressure, to kill microorganisms. Exposure for 15 min to steam at 15 psi—121°C is most commonly used. Such exposure kills vegetative bacterial cells and bacterial endospores. However, some substances do not tolerate such exposures and lower temperatures and different exposure times are sometimes employed. Media containing carbohydrates often are sterilized at 116°–118°C in order to prevent the decomposition of the carbohydrate and the formation of toxic compounds that would inhibit microbial growth. Below is a list of pressure–temperature relationships.
Pressure—psi Temperature—°C 0 1 2 3 4 5 6
100 101.9 103.6 105.3 106.9 108.4 109.8
Preparation of Media Pressure—psi Temperature—°C 7 111.3 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25
112.6 113.9 115.2 116.4 117.6 118.8 119.9 121.0 122.0 123.0 124.0 125.0 126.0 126.9 127.8 128.7 129.6 130.4
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followed by 15 min exposure during which the temperature is raised to 121°C using only steam under pressure in the chamber; the temperature then is slowly lowered to less than 60°C.
Filtration Filtration is commonly used to sterilize media containing heat-labile compounds. Liquid media are passed through sintered glass or membranes, typically made of cellulose acetate or nitrocellulose, with small pore sizes. A membrane with a pore size of 0.2mm will trap bacterial cells and, therefore, sometimes is called a bacteriological filter. By preventing the passage of microorganisms, filtration renders fluids free of bacteria and eukaryotic microorganisms, that is, free of living organisms, and hence sterile. Many carbohydrate solutions, antibiotic solutions, and vitamin solutions are filter sterilized and added to media that have been cooled to temperatures below 50°C.
Tyndallization
Caution about Hazardous Components
Exposure to steam at 100°C for 30 min will kill vegetative bacterial cells but not endospores. Such exposure can be achieved using flowing steam in an Arnold sterilizer. By allowing the medium to cool and incubate under conditions where endospore germination will occur and by repeating the 100°C–30 mi e exposure on three successive days the medium can be sterilized because all the endospores will have germinated and the heat exposure will have killed all the vegetative cells. This process of repetitive exposure to 100°C is called tyndallization, after its discoverer John Tyndall.
Some media contain components that are toxic or carcinogenic. Appropriate safety precautions must be taken when using media with such components. Basic fuchsin and acid fuchsin are carcinogens and caution must be used in handling media with these compounds to avoid dangerous exposure that could lead to the development of malignancies. Thallium salts, sodium azide, sodium biselenite, and cyanide are among the toxic components found in some media. These compounds are poisonous and steps must be taken to avoid ingestion, inhalation, and skin contact. Azides also react with many metals, especially copper, to form explosive metal azides. The disposal of azides must avoid contact with copper or achieve sufficient dilution to avoid the formation of such hazardous explosive compounds. Media with sulfur-containing compounds may result in the formation of hydrogen sulfide which is a toxic gas. Care must be used to ensure proper ventilation. Media with human blood or human blood components must be handled with great caution to avoid exposure to human immunodeficiency virus and other pathogens that contaminate some blood supplies. Proper handling and disposal procedures must be followed with blood-containing as well as other media that are used to cultivate microorganisms.
Inspissation Inspissation is a heat exposure method that is employed with high protein materials, such as eggcontaining media, that cannot withstand the high temperatures used in autoclaving. This process causes coagulation of the protein without greatly altering its chemical properties. Several different protocols can be followed for inspissation. Using an Arnold sterilizer or a specialized inspissator, the medium is exposed to 75°–80°C for 2 h on each of three successive days. Inspissation using an autoclave employs exposure to 85°–90°C for 10 min achieved by having a mixture of air and steam in the chamber,
Index A 1 Broth 9 A 3 Agar 5 A 3B Agar 5 A 7 Agar 6 A 7 Agar, Modified 7 A 7B Agar 7 A 8B Agar 8 AATCC Bacteriostasis Agar 201 AATCC Bacteriostasis Broth 201 Abeyta-Hunt Bark Agar 9 ABY Agar 10 AC Agar 10 AC Broth 10 AC Medium 10 Acanthamoeba Medium 11 Acanthamoeba species 11 ACC Medium 11 Acetamide Agar 11 Acetamide Broth 11 Acetamide Cetrimide Glycerol Mannitol Selective Medium 12 Acetamide Medium 12, 13 Acetate Differential Agar 13 Acetate fermentation 145 Acetobacteroides glycinophilus 14 Acetobacteroides glycinophilus Medium 13 Acetoin production 319, 473 Acholeplasma species 240 Achromobacter Choline Medium 14 Achromobacter Choline Medium, Modified 14 Achromobacter cholinophagum 14 Achromobacter Medium 15 Achromobacter species 15 Acid Bismuth Yeast Agar 10 Acid Egg Medium 15 Acid production 27, 46, 319 Acid Tomato Broth 15 Acinetobacter lwoffii 49 Acinetobacter species 242 Actidione® Agar 15 Actimomycetes 17 Actinobacillus lignieresii 371 Actinobacillus pleuropneumoniae 235 Actinobacillus species 81 Actinobacillus ureae 107 Actinobaculum spp 155 Actinomadura pelletieri 57 Actinomadura species 42, 116, 157, 228, 271, 341, 342, 468, 479 Actinomadura umbrina 56 Actinomyces Agar 16 Actinomyces bovis 58, 82 Actinomyces Broth 16 Actinomyces georgiae 58 Actinomyces gerencseriae 58
497
Actinomyces Isolation Agar 16 Actinomyces israelii 58, 82, 118, 322 Actinomyces naeslundii 58, 82, 100, 124, 211 Actinomyces odontolyticus 58, 79 Actinomyces species 16, 138, 154, 155 Actinomyces viscosus 58, 124, 211 Actinomycete Growth Medium 17 Actinomycetes 116, 343, 375, 407, 479 Actinoplanes caeruleus 229 Actinoplanes missouriensis 57 Actinoplanes philippinensis 57 Actinopolyspora species 42, 157, 271, 341 Activated Carbon Medium 17 AE Sporulation Medium, Modified 17 Aerial hyphae morphology 407 Aerobic bacteria 10, 75, 79, 161, 206, 207, 224, 225, 335, 336, 386, 407, 418, 420, 421, 453, 454, 455 Aerobic actinomycetes 140, 407, 465, 467 Aerobic Low Peptone Basal Medium 24 Aeromonas Differential Agar 18 Aeromonas hydrophila 18, 61, 192, 377 Aeromonas hydrophila Medium 18 Aeromonas Medium 18 Aeromonas salmonicida 204, 482, 484 Aeromonas species 18, 201, 259, 374, 384 AFPA 19 Agar diffusion technique 268, 269 Agar Listeria Ottavani & Agosti 23 Agar Medium A 34 Agar Medium C 35 Agars 487 AGS 39 AH5 Medium 19 AKI Medium 20 Albumin Fatty Acid Broth, Leptospira Medium 72 Albumin Fatty Acid Semisolid Medium, Modified 72 Alcaligenes Agar 20 Alcaligenes faecalis 21 Alcaligenes Medium 20 Alcaligenes N5 Medium 20 Alcaligenes NA YE Medium 21 Alcaligenes NB YE Agar 21 Alcaligenes NB YE Broth 21 Alcaligenes NB YE Medium 21 Alcaligenes Nutrient Agar Yeast Extract Medium 21 Alcaligenes Nutrient Broth Yeast Extract Agar 21 Alcaligenes Nutrient Broth Yeast Extract Broth 21 Alcaligenes Nutrient Broth Yeast Extract Medium 21 Alcaligenes species 15, 20, 21, 55 Alginate Utilization Medium 21 Aliphatic acid utilization 24 Alkaline Peptone Agar 22 Alkaline Peptone Salt Broth 22
498
Index
Alkaline Peptone Water 22 Alkvisco Medium 22 Allantoin Agar 22 Allantoin Broth 23 ALOA Medium 23 ALP Basal Medium 24 American Association of Textile Chemists and Colorists Bacteriostasis Agar 201 American Association of Textile Chemists and Colorists Bacteriostasis Broth 201 American Trudeau Society Medium 41 Amies Modified Transport Medium with Charcoal 24, 25 Amies Transport Medium without Charcoal 25 Amino acid decarboxylation 171 Ammonium compounds 280, 281 AMO.1 Medium 25 Amoebae species 180 Ampicillin Kanamycin Nutrient Agar 26 Ampicillin L Broth Medium 26 Ampicillin TY Salt Medium 27 Ampicillin Selective Supplement 491 Anaerobe Selcective Supplement GN 491 Anaerobe Selective Supplement NS 491 Amygdalin hydrolysis 27 Amygdalin Medium 27 Amylase production 46, 400, 401 Anaerobe Agar 27, 28 Anaerobe Medium 28 Anaerobes 10, 16, 29, 31, 32, 75, 79, 82, 83, 89, 118, 119, 120, 129, 134, 136, 138, 160, 161, 162, 166, 188, 198, 199, 200, 202, 206, 207, 212, 224, 225, 263, 283, 284, 286, 287, 288, 302, 303, 317, 365, 369, 376, 386, 387, 418, 420, 421, 433, 466, 477, 478 Anaerobic Agar 28, 29 Anaerobic Broth 29 Anaerobic CNA Agar 29 Anaerobic Colistin Nalidixic Acid Agar 29 Anaerobic Egg Yolk Agar 29, 30 Anaerobic indicator 344 Anaerobic LKV Blood Agar 30 Anaerobic Oxalate Medium 31 Anaerobic Trypticase Soy Agar with Calf Blood 32 Anaerobic Trypticase Soy Medium with Calf Blood 32 Anaerobic TVLS Medium 32 Andersen’s Pork Pea Agar 32 Andrade’s Broth 33 Animal tissue culture 184, 185, 186 Animal tissue culture cells 39 Anthracis Chromogenic Agar 34 Antibacterial testing 201 Antibiotic assay testing 34, 35, 36, 37
Antibiotic Medium 1 34 Antibiotic Medium 2 34 Antibiotic Medium 3 34 Antibiotic Medium 3 Plus 35 Antibiotic Medium 4 35 Antibiotic Medium 5 35 Antibiotic Medium 6 35 Antibiotic Medium 7 35 Antibiotic Medium 8 36 Antibiotic Medium 9 36 Antibiotic Medium 10 36 Antibiotic Medium 11 36 Antibiotic Medium 12 37 Antibiotic Medium 13 37 Antibiotic Medium 19 37 Antibiotic Medium 20 37 Antibiotic Medium 21 37 Antibiotic Sulfonamide Sensitivity Test Agar 38 Antibiotics 37, 38, 322 Antifungal 256 Antifungal agents 116, 117 Antimicrobial 38 Antimicrobial disc diffusion susceptibility testing 321 Antimicrobial sensitivity testing 177 Antimicrobial susceptibility 305, 306, 307, 308, 309, 313 Antimicrobial susceptibility (MIC) testing 478 Antimicrobial susceptibility testing 75, 116, 117, 176, 235, 262, 320, 477 Antiseptics 201 Anti-tubercular drugs 310, 311 AOAC Letheen Broth 38 APS Broth 22 Arabinose fermentation 389 Arcanobacterium spp. 154 Arenavirus Plaquing Medium 38 Arenaviruses 39 Arginine Broth 39 Arginine Broth with NaCl 39 Arginine decarboxylation 39 Arginine dihydrolase 315 Arginine Glucose Slants 39 Arizona species 412, 413 Armstrong Fusarium Medium 39 Arylsulfatase Agar 39 Ascospore Agar 40 Ascospores 40 Ascosporogenous yeasts 40 ASM Medium 40 Asparaginate Glycerol Agar 40 Asparagine Broth 40 Aspergillus amstelodami 41 Aspergillus awamori 41 Aspergillus Differential Medium 40
Index Aspergillus flavus 19, 41 Aspergillus flavus/parasiticus Agar 19 Aspergillus Medium 41 Aspergillus nidulans 41 Aspergillus parasiticus 19 ASS Agar 38 Assay testing 322 Association of Official Analytical Chemists Letheen Broth 38 Atopobium minutum 64, 211 ATS Medium 41 Autoclaving 494 AV Agar with Vitamins 41 Avian Mycoplasma Agar 42 Avian Mycoplasma Broth 42 Azide Agar 194 Azide Blood Agar 43 Azide Blood Agar with Crystal Violet 43 Azide Broth 44 Azide Citrate Broth 44 Azide Dextrose Broth 44 Azide Glucose Broth 44 Azide Medium 44 B Broth 44 Bacillus anthracis 34, 237, 270, 340, 361, 371 Bacillus cereus 34, 45, 49, 211, 237 Bacillus cereus Medium 44 Bacillus cereus Motility Medium 49 Bacillus cereus Selective Agar Base 45 Bacillus cereus Selective Supplement 491 Bacillus Medium 45, 46 Bacillus pseudogordonae 124 Bacillus species 23, 45, 46, 238, 363 Bacillus subtilis 35 Bacteriodes fragilis 46 Bacterionema helcogenes 472 Bacteroides Bile Esculin Agar 46 Bacteroides distasonis 64, 210 Bacteroides fragilis 60, 210, 418 Bacteroides gracilis 138, 209 Bacteroides melaninogenicus 118, 263 Bacteroides nodosus 472 Bacteroides ovatus 64, 210 Bacteroides pyogenes 472 Bacteroides salivosus 472 Bacteroides species 31, 46, 60, 89, 119, 137, 138, 211, 263, 286, 375, 386, 472 Bacteroides suis 472 Bacteroides thetaiotamicron 64, 118, 210 Bacteroides uniformis 64, 210 Bacteroides ureolyticus 97, 137, 138, 209 Bacteroides vulgatus 64, 210 BAF Agar 47 BAGG Broth 47 Baird–Parker Agar 47, 48
499
Baird–Parker Agar, Supplemented 48 Balamuth Medium 48 Balneatrix alpica 155 Bartonella bacilliformis 450 Bartonella elizabethae 239 Bartonella henselae 239 Bartonella quintana 239, 371 Basal Synthetic Medium 49 Base Agar 34 Base Agar with Low pH 36 Basic Cultivation Medium 49 Basic Mineral Medium 49 Bauer-Kirby method 321 BBE Agar 46 BBGS Agar 61 BC Motility Medium 49 BCG vaccine 385 BCM 44 BCM Bacillus cereus Group Plating Medium 49 BCM for Listeria monocytogenes 62 BCM O157 H7(+) Plating Medium 50 BCP Broth 85 BCP D Agar 50 BCP DCLS Agar 50 BCYE α Agar, Modified 277 BCYE Agar 50 BCYE alpha Base 50 BCYE Differential Agar 51 BCYE Medium, Diphasic Blood Culture 51 BCYE Selective Agar with CCVC 52 BCYE Selective Agar with GPVA 52 BCYE Selective Agar with GVPC 53 BCYE Selective Agar with PAC 53 BCYE Selective Agar with PAV 54 BCYEα with Alb 54 BCYEα without L-Cysteine 54 Beef extract 489 Beef Extract Agar 55 Beef Extract Broth 55 Beef Extract Peptone Serum Medium 55 Beef Heart 489 Beef Infusion Agar 55 Beef Infusion Broth 56 Beef Liver Medium for Anaerobes 55 Bennett’s Agar 56 Bennett’s Agar with Maltose 56 Bennett’s Modified Agar Medium 56 Beta hemolytic streptococci 396 BG Sulfa Agar 56 BHI 74 BHI Agar 75 BHI Agar 0.7% 75 BHI Broth 79 BHI Glucose Medium 57
500
Index
BHI Medium 58 BHI with Glucose 57 BHI with Glycerol and Reducing Agents 57 BHI/1 Medium 58 BHI/2 Medium 58 BHI/3 Medium 58 Bifidobacterium adolescentis 472 Bifidobacterium bifidum 472 Bifidobacterium breve 472 Bifidobacterium infantis 58 Bifidobacterium longum 472 Bifidobacterium Medium 58 Bifidobacterium species 58, 64, 137, 211, 376, 422 BiGGY Agar 59 Bile Esculin Agar 59 Bile Esculin Agar with Kanamycin 60 Bile Esculin Azide Agar 60 Bile Oxalate Sorbose Broth 60 Bile Salts Brilliant Green Starch Agar 61 Bile Salts Gelatin Agar 61 Bile tolerance 59, 60, 410 BIN Medium 62 Biosynth Chromogenic Medium for Listeria monocytogenes 62 Biphasic Medium for Neisseria 62 Bird Seed Agar 63 Bismuth Sulfite Agar 63 Bismuth Sulfite Broth 64 Bismuth Sulfite Glucose Glycerin Yeast Extract Agar 59 BL Agar 64 Blaser’s Agar 108 Blaser’s Campylobacter Agar 101 Blaser-Wang Campylobacter Medium 108, 109 Blastocrithidia culicis 179 Blastocrithidia leptocoridis 79 Blastomyces dermatitidis 74, 80, 252, 254, 360, 380, 483 Blood 65, 89, 125, 154, 175, 277, 305, 312, 380, 399, 469 Blood Agar 64 Blood Agar Base 65 Blood Agar Base No. 2 65 Blood Agar Base with Peptone 66 Blood Agar Base with Special Peptone 66 Blood Agar Base, Sheep 66 Blood Agar No. 2 67 Blood Agar with Low pH 67 Blood Agar, Diphasic 66 Blood Agar, Diphasic Base Medium 67 Blood Base Agar 67 Blood Base Agar with Charcoal 67 Blood Base Agar with Horse Blood 68 Blood Base Agar with Horse Blood, Fumarate and Formate 68 Blood culture 75
Blood Glucose Cystine Agar 68 BMPA–α Medium 68, 69 Body fluids 322, 422 Bonner–Addicott Medium 69 Bordet Gengou Agar 70, 71 Bordetella bronchiseptica 331 Bordetella parapertussis 70, 71, 241, 375, 376 Bordetella pertussis 70, 71, 126, 263, 375, 376 Bordetella pertussis Selective Medium with Bordet-Gengou Agar Base 69 Bordetella pertussis Selective Medium with Charcoal Agar Base 70 Bordetella Selective Supplement 491 Bordet-Gengou Medium 71 Borrelia afzelii 96 Borrelia anserina 96 Borrelia burgdorferi 95, 96, 265, 266 Borrelia garinii 96 Borrelia gorinii 95 Borrelia hermsii 72 Borrelia japonica 96 Borrelia Medium 71 Borrelia parkeri 72 Borrelia species 94 Borrelia turicatae 72 BOS Broth 60 Botulism 146 Bouillon Medium 72 Bovine albumin 489 Bovine Albumin Tween 80 Medium, Ellinghausen and McCullough, Modified 72 Bovine Albumin Tween 80 Semisolid Medium, Ellinghausen and McCullough, Modified 72 Bovine blood, citrated 489 Bovine blood, defibrinated 489 Bovine Serum Albumin Tween 80 Agar 73 Bovine Serum Albumin Tween 80 Broth 73 Bovine Serum Albumin Tween 80 Soft Agar 74 Brain Heart CC Agar 74 Brain Heart Cycloheximide Chloramphenicol Agar 74 Brain Heart Infusion 74 Brain Heart Infusion Agar 75, 79 Brain Heart Infusion Agar 0.7% 75 Brain Heart Infusion Agar with 10% Sheep Blood, Gentamicin and Chloramphenicol 77 Brain Heart Infusion Agar with Chloramphenicol 76 Brain Heart Infusion Agar with Kanamycin 76 Brain Heart Infusion Agar with Penicillin and Streptomycin 76 Brain Heart Infusion Agar with Tween 80 77 Brain Heart Infusion Blood Agar 78 Brain Heart Infusion Broth 79 Brain Heart Infusion Casein Starch 79 Brain Heart Infusion Soil Extract Medium 81
Index Brain Heart Infusion with 0.7% Agar 76 Brain Heart Infusion with 3% Sodium Chloride 81 Brain Heart Infusion with 5% NaCl 80 Brain Heart Infusion with Agar, Yeast Extract, NaCl, Inactivated Horse Serum and Penicillin 80 Brain Heart Infusion with Agar, Yeast Extract, NaCl, Inactivated Horse Serum, and Penicillin 77 Brain Heart Infusion with Agar, Yeast Extract, Sucrose, Horse Serum, and Penicillin 78 Brain Heart Infusion with Agar, Yeast Extract, Sucrose, Inactivated Horse Serum, and Penicillin 78 Brain Heart Infusion with Casein 79 Brain Heart Infusion with Cystine 79 Brain Heart Infusion with Glucose and Horse Serum 80 Brain Heart Infusion with PABA 80 Brain Heart Infusion with PABA and Agar 80 Brain Heart Infusion with p-Aminobenzoic acid 80 Brain Heart Infusion with p-Aminobenzoic acid and Agar 80 Brain Heart Infusion with Rabbit Serum 81 Brain Heart Infusion with Sucrose and Horse Serum 82 Brain Liver Heart Semisolid Medium 82 Branhamella catarrhalis 58, 213, 214 Brevibacterium Medium 82 Brewer Anaerobic Agar 82 Brewer Thioglycollate Medium 82 Brewer Thioglycollate Medium, Modified 82 BRILA 84 BRILA MUG Broth 83 Brillant Green 2%-Bile MUG Broth 83 Brilliant Green 2%-Bile Broth, Fluorocult® 84 Brilliant Green Agar 83 Brilliant Green Agar, Modified 83 Brilliant Green Lactose Bile Broth 84 Brilliant Green Phenol Red Agar 84 Brilliant Green Sulfapyridine Agar 56 Brochothrix thermosphacta 227 BROLACIN MUG Agar 84 Bromcresol Purple Broth 85 Bromcresol Purple Deoxycholate Agar 50 Bromcresol Purple Deoxycholate Citrate Lactose Sucrose Agar 50 Bromcresol Purple Dextrose Broth 85 Bromothymol Blue Lactose Cystine MUG Agar 84 Bromthymol Blue Agar 85 Bromthymol Blue Broth 86 Bromthymol Blue Lactose Agar 96 Broth dilution susceptibility testing method 256 Brucella Agar 86 Brucella Agar Base– Campylobacter Medium 87 Brucella Agar with Vitamin K1 87 Brucella Albimi Broth 89 Brucella Albimi Broth with 0.16% Agar 87 Brucella Albimi Broth with 0.16% Agar and 1% Glycine 87
501
Brucella Albimi Broth with Formate and Fumarate 88 Brucella Albimi Broth with Sheep Blood 88 Brucella Albimi Medium, Semisolid 88 Brucella Anaerobic Blood Agar 88 Brucella Blood Agar with Hemin and Vitamin K1 89 Brucella Blood Culture Broth 89 Brucella Broth 89 Brucella Broth Base Campylobacter Medium 91 Brucella Broth with 0.16% Agar 90, 449 Brucella Broth with Additives 90 Brucella Broth, Modified 91 Brucella FBP Agar 91 Brucella FBP Broth 91 Brucella Medium Base 92 Brucella Medium, Selective 92 Brucella Selective Medium 92 Brucella Selective Supplement 491 Brucella Semisolid Medium with Cysteine 92 Brucella Semisolid Medium with Glycine 93 Brucella Semisolid Medium with NaCl 93 Brucella Semisolid Medium with Nitrate 93 Brucella species 66, 86, 87, 90, 91, 92, 283, 390, 391, 453, 454, 455 BSA Tween 80 Agar 73 BSA Tween 80 Broth 73 BSA Tween 80 Soft Agar 74 BSK Medium 94 BSK Medium, Modified 94 BSK Medium, Revised 95 BTB Lactose Agar 96 BTB Teepol® Agar 96 BTU Medium 97 Buffered Azide Glucose Glycerol Broth 47 Buffered Charcoal Yeast Extract Agar 50 Buffered Charcoal Yeast Extract Agar with Albumin 54 Buffered Charcoal Yeast Extract Agar without L-Cysteine 54 Buffered Charcoal Yeast Extract Differential Agar 51, 97 Buffered Charcoal Yeast Extract Medium, Diphasic Blood Culture 51 Buffered Charcoal Yeast Extract Selective Agar with Cephalothin, Colistin, Vancomycin, and Cycloheximide 52 Buffered Charcoal Yeast Extract Selective Agar with Glycine, Polymyxin B, Vancomycin, and Anisomycin 52 Buffered Charcoal Yeast Extract Selective Agar with Glycine, Vancomycin, Polymyxin B, and Cycloheximide 53 Buffered Charcoal Yeast Extract Selective Agar with Polymyxin B, Anisomicin, and Vancomycin 54 Buffered Charcoal Yeast Extract Selective Agar with Polymyxin B, Anisomycin, and Cefamandole 53
502
Index
Buffered Enrichment Broth 97 Buffered Peptone Water 98 Buffered Yeast Extract Broth 99 Burkholderia cepacia 98 Burkholderia cepacia Agar 98 Burkholderia species 374 Butzler’s Campylobacter Medium 109 BYE Agar 98 BYEB 99 C.L.E.D. MUG Agar 84 CA YE Broth 116 Cadmium Fluoride Acriflavin Tellurite Medium 124 CAFC Test Medium 99 Caffeic Acid Agar 99 Caffeic Acid Ferric Citrate Test Medium 99 Caffeine Medium 99 CAL Agar 100 CAL Broth 100 Calymmatobacterium granulomatis 100, 182 Calymmatobacterium granulomatis Semidefined Medium 100 CAMG Broth 100 CAMP test 446, 447 Camplyobacter Selective Medium, Blaser-Wang 109 Campy BAP Medium 108 Campy Cefex Agar 107 Campy THIO Medium 100 Campylobacter Agar 101 Campylobacter Agar with 5 Antimicrobics and 10% Sheep Blood 101 Campylobacter Agar, Blaser’s 101 Campylobacter Agar, Skirrow’s 102 Campylobacter Blood-Free Agar Base Modified 102 Campylobacter Blood-Free Selective Agar 102 Campylobacter Charcoal Differential Agar 103 Campylobacter coli 90, 91, 103, 443, 472 Campylobacter concisus 472 Campylobacter curvus 108 Campylobacter divergens 64, 211 Campylobacter Enrichment Broth 103, 104 Campylobacter fecalis 90, 91, 105 Campylobacter fecalis Medium 105 Campylobacter fetus 91, 106, 206, 472 Campylobacter fetus Medium 105, 106 Campylobacter fetus Selective Medium 106 Campylobacter gracilis 339 Campylobacter growth supplement 489 Campylobacter hyointestinalis 472 Campylobacter Isolation Agar A 106 Campylobacter Isolation Agar B 107 Campylobacter jejuni 87, 91, 101, 102, 103, 111, 206, 443, 472 Campylobacter lari 472 Campylobacter laridis 103 Campylobacter Medium 107
Campylobacter mucosalis 88, 108, 138, 472 Campylobacter mucosalis Medium 107 Campylobacter rectus 108, 339 Campylobacter rectus Medium 108 Campylobacter Selective Medium, Blaser-Wang 108 Campylobacter Selective Medium, Butzler’s 109 Campylobacter Selective Medium, Karmali’s 110 Campylobacter Selective Medium, Preston’s 110 Campylobacter Selective Supplement Blaser-Wang 491 Campylobacter Selective Supplement Butzler 492 Campylobacter Selective Supplement Preston 492 Campylobacter Selective Supplement Skirrow 492 Campylobacter species 10, 87, 88, 92, 93, 101, 102, 103, 104, 105, 107, 108, 109, 110, 111, 164, 167, 209, 210, 336, 388, 394, 443 Campylobacter sputorum 58, 111, 472 Campylobacter sputorum subspecies bubulus 111 Campylobacter sputorum subspecies bubulus Medium 110 Campylobacter sputorum subspecies mucosalis 111 Campylobacter sputorum subspecies mucosalis Medium 111 Campylobacter Thioglycollate Medium with 5 Antimicrobics 111 Campylocbacter pylori 213, 214 Candida albicans 10, 59, 112, 127, 140, 170, 315, 349, 377, 431, 479 Candida BCG Agar Base 111 Candida Bromcresol Green Agar Base 111 Candida Isolation Agar 112 Candida kefyr 479 Candida krusei 59, 112, 315 Candida parakrusei 59 Candida pseudotropicalis 59, 112 Candida species 10, 59, 112, 127, 140, 142, 315, 349, 377 Candida stellatoidea 59, 112, 315, 377 Candida tropicalis 10, 59, 112, 140, 315, 479 Capnocytophaga gingivalis 472 Capnocytophaga granulosa 112 Capnocytophaga haemolytica 112 Capnocytophaga II Medium 112 Capnocytophaga Medium 112 Capnocytophaga ochracea 472 Capnocytophaga species 112, 137 Capnocytphaga sputigena 472 Caprylate Thallous Agar 165 Capsule production 479 Carbohydrate 355, 368, 369, 453 Carbohydrate assimilation 114, 475, 476 Carbohydrate fermentation 33, 34, 113, 183, 193, 202, 207, 282, 348, 353, 397, 445, 484 Carbohydrate Fermentation Broth 112 Carbohydrate Medium Base 129
Index Carbon Assimilation Medium 113 Carbon Assimilation Medium, Auxanographic Method for Yeast Identification 113 Carbon source 14, 22, 24, 115, 133, 139, 140, 144, 259, 298, 345, 394 Carbon Utilization Test 114 Cardiobacterium hominis 114 Cardiobacterium hominis Medium 114 Carnitine Chloride Medium 114 Carrot Potato Dextrose Agar 115 Cary and Blair Transport Medium 115 Cary and Blair Transport Medium, Modified 115 Casamino acids 489 Casamino Acids Yeast Extract Lincomycin Medium 116 Casamino Acids Yeast Extract Salts Broth, Gorbach 116 Casein Agar 116 Casein hydrolysate 487 Casein Medium 116 Casein Yeast Extract Glucose Agar 116 Casein Yeast Extract Glucose Broth 117 Casitone 487 Casman Agar Base 117 Casman Agar Base with Rabbit Blood 117 Casman-Medium 117 CASO MUG Agar 117 Catalase production 287 Castenholtz Salts 489 Cautions 495 CBI Agar 145 CCDA 103 CCDA, Modified 102 CCDA Selective Supplement 492 CCFA 146 CCY Modified Medium 118 CDC Anaerobe Blood Agar 118 CDC Anaerobe Blood Agar with Kanamycin and Vancomycin 118 CDC Anaerobe Blood Agar with PEA 119 CDC Anaerobe Blood Agar with Phenylethyl Alcohol 119 CDC Anaerobe Laked Blood Agar with Kanamycin and Vancomycin 119 CDC Anaerobe Laked Blood Agar with KV 119 CDC Modified McClung – Toabe Egg Yolk Agar 302 Cefiximine Rhamnose Sorbitol MacConkey Agar 120 Cefoperazone Selective Supplement 492 Cefoperazone Vancomycin Amphotericin Medium 167 Cefsulodin Irgasan® Novobiocin Agar 120, 144 Cell Growth Medium 121 Cell lines 184, 185, 186, 424, 425, 426, 427 Cellobiose Arginine Lysine Agar 100 Cellobiose Arginine Lysine Broth 100 Cellobiose Polymyxin B Colistin Agar, Modified 122
503
Cellobiose Polymyxin Colistin Agar 123 Cereal Agar 123 Cetoin production 319 Cetrimide Agar, Non-USP 123 Cetrimide Agar, USP 123 CF Assay Medium 123 CFAT Medium 124 CFC Selective Supplement 492 CGY Agar 124 CH 1 Medium 124 Chapman Stone Agar 125 Chapman Tellurite Solution 492 Charcoal Agar 125 Charcoal Agar Slants 179 Charcoal Agar with Horse Blood 125 Charcoal Agar with Horse Blood and Cepahalexin 125 Charcoal Blood Medium 126 Charcoal Yeast Extract Agar 167 Charcoal Yeast Extract Agar, Buffered 168 Charcoal Yeast Extract Diphasic Blood Culture Medium 277 Chlamydia Growth Medium 126 Chlamydia Isolation Medium 127 Chlamydia species 127, 406 Chlamydospore Agar 127 Chlamydospore formation 127, 377 Chlamydospore production 170 Chlamydospores 431, 479 Chloramphenicol Ampicillin LB Medium 127 Chloramphenicol Erythromycin LB Medium 128 Chloramphenicol L Broth Medium No. 1 128 Chloramphenicol L Broth Medium No. 2 128 Chloramphenicol L Broth Medium No. 3 129 Chloramphenicol LB Medium No. 2 129 Chloramphenicol LB Medium No.1 129 Chloramphenicol Selective Supplement 492 Chlorinated Fatty Acid Medium 129 CHO Medium 201 CHO Medium Base 129 Chocolate Agar 129, 130 Chocolate Agar, Enriched 130, 131 Chocolate Agar-Bartonella C-29 131 Chocolate II Agar 132 Chocolate II Agar with Hemoglogin and IsoVitaleX® 132 Chocolate Tellurite Agar 132 Cholera enterotoxin 482 Cholera Medium TCBS 133 Cholic Acid Medium 133 Chopped Meat Agar 134 Chopped Meat Broth 134 Chopped Meat Broth with Carbohydrates 134 Chopped Meat Broth with Formate and Fumarate 134 Chopped Meat Broth with Vitamin K1 135 Chopped Meat Carbohydrate Medium 135
504
Index
Chopped Meat Glucose Agar 136 Chopped Meat Glucose Broth 136 Chopped Meat Glucose Medium 136 Chopped Meat Medium 136 Chopped Meat Medium with Formate and Fumarate 137 Chopped Meat Medium, Modified 137 Chopped Meat Medium, Modified with Formate and Fumarate 138 Christensen Agar 139 Christensen Citrate Agar 139 Christensen Citrate Agar, Modified 139 Christensen Citrate Sulfide Medium 139 Christensen’s Urea Agar 140 CHROMagar Candida 140 CHROMagar E. coli 140 CHROMagar ECC 140 CHROMagar Listeria 141 CHROMagar O157 141 CHROMagar Orientation 141 CHROMagar Salmonella 141 CHROMagar Staph. aureus 141 CHROMagar Vibrio 141 Chromatiaceae Medium 1 143 Chromocult Coliform Agar 153 Chromocult Coliform Agar ES 153 Chromocult Enhanced Selectivity Agar 153 Chromocult Enterococci Broth 193 Chromocult® TBX 451 ChromocultTryptone Bile X-glucuronide Agar 451 Chromogenic Candida Agar 142 Chromogenic Listeria Agar 142 Chromogenic MRSA Agar 142 Chromogenic Salmonella Esterase Agar 143 Chromogenic Substrate Broth 143 Chromogenic Urinary Tract Infection (UTI) Medium 143 Chromogenic UTI Medium, Clear 144 CIN Agar 120, 144 Citrate Agar 139, 393 Citrate Medium, Koser’s Modified 144 CLED Agar 145 CLED Agar with Andrade Indicator 145 Clinical specimens 19, 47, 70, 71, 75, 76, 77, 86, 89, 97, 101, 115, 116, 118, 119, 120, 124, 132, 144, 146, 147, 152, 154, 156, 157, 167, 182, 198, 199, 200, 210, 211, 212, 222, 223, 230, 237, 241, 263, 269, 272, 274, 276, 278, 296, 299, 300, 319, 324, 332, 334, 335, 353, 358, 364, 373, 375, 376, 379, 380, 381, 388, 399, 400, 404, 408, 418, 421, 448, 449, 451, 456, 462, 463, 464, 468, 485 Clostridia Medium 145 Clostridium botulinum 146, 283, 302, 397, 445, 446, 455 Clostridium botulinum Isolation Agar 145
Clostridium CK Medium 146 Clostridium colinum 472 Clostridium difficile 146, 147, 167, 472 Clostridium difficile Agar 146 Clostrideium difficile Selective Supplement 492 Clostridium estertheticum Medium 147 Clostridium haemolyticum 118 Clostridium histolyticum 276 Clostridium Medium 147, 148, 149 Clostridium novyi 150, 276 Clostridium novyi Blood Agar 149 Clostridium oxalicum 32 Clostridium perfringens 18, 150, 182, 249, 261, 274, 276, 283, 301, 303, 317, 397, 418, 446, 456, 457, 458 Clostridium perfringens Agar, OPSP 150 Clostridium Selective Agar 150 Clostridium septicum 276 Clostridium sordelli 276 Clostridium species 28, 29, 30, 33, 56, 57, 135, 136, 137, 138, 145, 146, 147, 148, 149, 150, 188, 189, 211, 225, 261, 274, 276, 282, 286, 302, 376, 455 Clostridium spiroforme 472 Clostrisel Agar 150 CM3 Medium 150 CMA 162 CMYG 163 CN Inhibitor 492 CN Screen Medium 151 CNV Antimicrobic 492 CNVT Antimicrobic 492 Coagulase Agar Base 151 Coagulase Mannitol Agar 151 Coagulase production 151 Coagulase-positive staphylococci 47, 48, 197, 409 COBA 151 Coccidioides immitis 75, 81, 160, 483 Colbeck’s Egg Broth 492 Coletsos Medium 152 Coletsos Selective Medium 152 Coliform 84, 143, 189, 190, 191, 192, 275, 281, 297, 398, 409, 473 Coliform Agar ES, Chromocult 153 Coliform Agar, Chromocult® 153 Coliform bacteria 297 Coliform microorganisms 201 Coliform Rapid HiCrome Broth 249 Coliforms 83, 139, 140, 144, 153, 244, 273, 284, 295, 296, 297, 298, 304, 409, 410, 451 Colistin Oxolinic Acid Blood Agar 151 Colony characteristics 145 Columbia Agar 154 Columbia Blood Agar 154 Columbia Blood Agar Base 154 Columbia Blood Agar Base with Horse Blood 155
Index Columbia Blood Agar Base with Horse Blood and Charcoal 155 Columbia Broth 155, 156 Columbia CNA Agar 156 Columbia CNA Agar, Modified with Sheep Blood 156 Columbia Colistin Nalidixic Acid Agar 156 Comamonas acidovorans 177 Comamonas testosteroni 257, 340 Complex Medium 157 Congo Red Acid Morpholinepropanesulfonic Acid Pigmentation Agar 157 Congo Red Agar 157, 158 Congo Red BHI Agarose Medium 158, 159 Congo Red Magnesium Oxalate Agar 159 Conradi Drigalski Agar 159 Converse Liquid Medium, Levine Modification 160 Cooke Rose Bengal Agar 160 Cooked Meat Medium 160, 161 Cooked Meat Medium with Glucose, Hemin, and Vitamin K 161 Cooked Meat Medium with Peptone and Yeast Extract 162 Cooked Meat Medium, Modified 161 Corn Meal Agar 162 Corn Meal Agar with Strep100 and Tet100 162 Corn Meal Phytophthora Isolation Medium No. 1 162 Corn Meal Yeast Glucose Agar 163 Cornmeal and V8 Juice Agar 162 Corynebacterium diphtheriae 133, 169, 255, 256, 268, 269, 285, 289, 290, 354, 371, 422 Corynebacterium diphtheriae Virulence Test Medium 268 Corynebacterium genitalium 451, 452 Corynebacterium minutissimum 57 Corynebacterium pseudogenitalium 452 Corynebacterium pseudotuberculosis 239 Corynebacterium species 22, 57, 58, 90, 133, 155, 238, 276, 349, 370, 392 Corynebacterium vaginale 301, 400, 401 CPC Agar 123 CR Agar 157, 158 CRAMP Agar 157 CRBHO Medium 159 CREA 163 Creatine Agar 163 Creatinine Agar 163 Creatinine Medium 163 CreDm1 Medium 164 Crithidia deanei 179 Crithidia flexonema 179 Crithidia mellificae 179 CRMOX Agar 159 CR-SMAC Agar Base 120 Cryptococcus species
505
Cryptococcus albidus 479 Cryptococcus neoformans 63, 99, 151, 259, 431 Cryptococcus neoformans Screen Medium 151 Cryptococcus species 63, 99, 259, 431, 486 Crystal Violet Agar 164 Crystal Violet Azide Esculin Agar 165 Crystal Violet Esculin Agar 165 CSE Agar 143 CT Agar 165 CTA Agar 166 CTA Medium 166 CTA Medium with Yeast Extract and Rabbit Serum 166 CTLM Medium 166 CVA Enrichment 489 CVA Medium 167 Cyanide production 27 Cycloheximide Agar 15 Cycloheximide Chloramphenicol Agar 324 Cycloserine Cefoxitin Egg Yolk Fructose Agar 167 Cycloserine Cefoxitin Fructose Agar 146 CYE Agar 167 CYE Agar, Buffered 168 CYE–DBCM 277 CYG Agar 116 CYG Broth 117 Cylinder plate technique 35 Cysteine Sulfide Reducing Agent 489 Cysteine Tellurite Blood Agar 169 Cystine Heart Agar 168 Cystine Heart Agar with Rabbit Blood 169 Cystine Lactose Electrolyte Deficient Agar 145 Cystine Lactose Electrolyte Deficient Agar with Andrade Indicator 145 Cystine Tryptic Agar 166 Cystine Trypticase Agar Medium 166 Cystine Trypticase Agar 166 Cystine Trypticase Agar Medium with Yeast Extract and Rabbit Serum 166 Cytopathogenicity 425 Czapek Agar with Sucrose 169 Czapek Dox Agar, Modified 169 Czapek Dox Broth 170 Czapek Dox Liquid Medium, Modified 170 Czapek Solution Agar 170 Czapek Yeast Extract Agar 170 DCLS Agar 171 Decarboxylase Base, Møller 171 Decarboxylase Medium Base, Falkow 171 Decarboxylase Medium, Ornithine Modified 171 Delayed-incubation total coliform procedure 398 DeMan, Rogosa, Sharpe Agar 319 DeMan, Rogosa, Sharpe Broth 319 Demi-Fraser Broth 172 Dental caries 394, 395
506
Index
Dental plaque 224, 225, 375 Deoxycholate Agar 172 Deoxycholate Citrate Agar 172, 173 Deoxycholate Citrate Agar, Hynes 173 Deoxycholate Citrate Lactose Sucrose Agar 171 Deoxycholate Lactose Agar 173 Deoxyribonuclease 180, 181 Deoxyribonuclease production 432 Dermasel Agar Base 174 Dermatophilus congolensis 57, 205 Dermatophyte Test Medium Agar 182 Dermatophyte Test Medium Base 174 Dermatophytes 283, 379, 380, 381 Dermatophytic fungi 174, 182 Desoxycholate Agar 172 Desoxycholate Citrate Agar 173 DEV Lactose Peptone MUG Broth 174 Dextrin fermentation 18 Dextrin Fuchsin Sulfite Agar 18 Dextrose Agar 174, 175 Dextrose Ascitic Fluid Semisolid Agar 175 Dextrose Broth 175 Dextrose Proteose No. 3 Agar 175 Dextrose Starch Agar 176 Diagnostic bacteriology 421 Diagnostic Sensitivity Test Agar 176 Diagnostic test 22 Diamonds Medium, Modified 177 Diethyl Phosphonate Agar 177 DIFF/BCYE 97 Differential Agar Medium A8 for Ureaplasma urealyticum 177 Differential Broth for Lactic Streptococci 178 Differential Components 494 Dilute Peptone Water 178 Dilute Potato Medium 178 Diphasic Blood Agar Base Medium 178 Diphasic Blood Agar Medium with 10% Blood 178 Diphasic Blood Agar Medium with 30% Blood 179 Diphasic Blood Culture Buffered Charcoal Yeast Extract Medium 277 Diphasic Medium for Amoeba 179 Diphtheria 392 Disc plate technique 362 Disinfectant products 38 Disinfectants 201 Dixon Agar 180 DNase Agar 180 DNase Medium 180 DNase production 432 DNase Test Agar 181 DNase Test Agar with Methyl Green 181 DNase Test Agar with Toluidine Blue 181 Dorset Egg Medium 181 Drug resistant 310, 311, 371
DS Sporulation Medium, Modified 182 DST AGAR 176 DST Agar 176 DTC Agar 181 DTM Agar 182 Dubos Medium Albumin 489 Dubos Oleic Albumin Complex 489 Ducreyi Medium, Revised 233 Dulaney Slants 182 Duncan–Strong Sporulation Medium, Modified 182 Dunkelberg Agar 352 Dunkelberg Carbohydrate Medium, Modified 182 Dunkelberg Maintenance Medium 183 Dunkelberg Semisolid Carbohydrate Fermentation Medium 183 E. coli 83, 84, 85, 144, 153, 174, 208, 246, 284, 297, 304, 361, 407, 4451, 52, 473 E. coli O157:H7 50, 183, 208, 248, 372 E. coli O157:H7 Agar, Fluorocult 208 E. coli O157:H7 MUG Agar 183 Eagle Medium 183, 184, 185 Eagle Medium, Modified 185 Eagle’s Minimal Essential Medium with Earle’s Salts and Nonessential Amino Acids 186 Earle’s Balanced Salts, Phenol Red–Free 183 EB Motility Medium 187 EC Broth 187 EC Broth with MUG 187 EC Medium, Modified with Novobiocin 187 ECD MUG Agar 188 Ecithinase production 302 Edelstein BMPA–a Medium 68 Egg Tellurite Glycine Pyruvate Agar 196 Egg Yolk Agar 188 Egg Yolk Agar with Neomycin 288 Egg Yolk Agar, Lombard–Dowell 287 Egg Yolk Agar, Modified 188 Egg Yolk Emulsion 189, 489 Egg Yolk Emulsion, 50% 189, 489 EHEC serovar BCM O157:H7(+) 50 Eijkman Lactose Medium 189, 190 Eikenella corrodens 214 Elek Agar 268 EMB Agar 190 EMB Agar Base 190 EMB Agar, Modified 190 Encephalitozoon cuniculi 314 Encephalitozoon hellem 314 Encephalitozoon intestinalis 314 Endo Agar 190, 191 Endo Agar, Laurance Experimental Station 191 Endo Agar, LES 191 Endo Broth 192 Endotrypanum species 179 Enriched Nutrient Broth 192
Index Enrichment Broth for Aeromonas hydrophila 192 Entamoeba histolytica 49, 193, 351 Entamoeba Medium 192 Entamoeba species 460, 485 Enteric bacteria 50, 63, 64, 160, 172, 191, 298, 383 Enteric Fermentation Base 193 Enteric pathogens 139, 140, 173, 174, 295, 296, 297, 480 Enterobacteaceae 453 Enterobacter aerogenes 271 Enterobacter agglomerans 294 Enterobacter Medium 193 Enterobacter species 59, 60, 172, 193, 195, 298 Enterobacteria 251 Enterobacteriaceae 33, 34, 59, 60, 86, 113, 139, 140, 263, 264, 270, 294, 297, 313, 317, 318, 345, 368, 369, 393, 443, 465, 466, 467, 468, 471 Enterococci 59, 60, 194, 196, 197, 247, 250, 267, 296, 297, 304, 392, 395, 413, 474, 475 Enterococci Broth, Chromocult 193 Enterococci HiCrome Broth 247 Enterococci Rapid HiCrome Agar 250 Enterococcosel Agar 194 Enterococcosel Broth 194 Enterococcus 373 Enterococcus Agar 194 Enterococcus avium 204 Enterococcus cecorum 155 Enterococcus columbae 155 Enterococcus faecalis 204, 363, 404 Enterococcus faecium 195, 204 Enterococcus faecium Medium 195 Enterococcus parauberis 155 Enterococcus pseudoavium 155 Enterococcus raffinosus 155 Enterococcus saccharolyticus 155 Enterococcus species 141, 143, 144, 203, 354, 449 Enterotoxigenic Escherichia coli 116 Enterotoxigenic staphylococci 399 Enterotoxin production 76 Enterovirulent Escherichia coli 319, 320 Eosin Methylene Blue Agar 190 Eosin Methylene Blue Agar, Levine 281 Eosin Methylene Blue Agar, Modified 190 Erysipelothris tonsillarum 455 Erysipelothrix rhusiopathiae 43, 107, 165 Erythritol Agar 195 Erythritol Broth 195 Escherichia coli 13, 27, 35, 84, 116, 122, 128, 129, 141, 158, 172, 187, 188, 189, 190, 230, 236, 242, 244, 245, 246, 247, 249, 258, 260, 271, 272, 275, 281, 332, 340, 365, 366, 372, 383, 396, 445, 452, 482 Escherichia coli Broth 187 Escherichia coli enterotoxin 482
507
Escherichia coli O157:H7 120, 188, 208, 249, 342 Esculin Agar 195 Esculin Agar, Lombard–Dowell 287 Esculin Agar, Modified CDC 195 Esculin Broth 195 Esculin hydrolysis 46 Esculin hydrolysis 59, 60, 287 Esculin Iron Agar 196 Esculin Mannitol Agar 196 Esculin Thallium Medium 196 ETGPA 196 Ethyl Violet Azide Broth 197 Eubacterium alactolyticum 211 Eubacterium combesii 386 Eubacterium contortum 386 Eubacterium Medium 198 Eubacterium species 16, 136, 137, 138, 198 EVA Broth 197 Excellospora species 42, 157, 271, 341 EY Tellurite Enrichment 489 FAA 198 FAA Alternative Selective 198 FAA Alternative Selective with Neomycin, Vancomycin, and Josamycin 199 FAA Selective 199 FAA Selective with Neomycin and Vancomycin 200 Falcivibrio grandis 472 Falcivibrio vaginalis 472 Fastidious Anaerobe Agar 198 Fastidious Anaerobe Agar, Alternative Selective 198 Fastidious Anaerobe Agar, Alternative Selective with Neomycin, Vancomycin, and Josamycin 199 Fastidious Anaerobe Agar, Selective 199 Fastidious Anaerobe Agar, Selective with Neomycin and Vancomycin 200 Fastidious bacteria 68, 117, 340 Fastidious fungi 77, 78, 82 Fastidious microorganisms 82, 130, 454 Fay and Barry Medium 200 FCIC 201 FDA Agar 201 FDA Broth 201 Fecal 47, 50, 87, 91, 100, 101, 102, 111, 146, 150, 194, 195, 197, 267, 436, 441 Fecal Coliform Agar, Modified 201 Fecal coliforms 9, 201 Fecal enterococci 197 Fecal specimens 50, 87, 100, 101, 102, 111, 146, 150, 171, 315, 384, 410, 412, 413 Fecal streptococci 47, 195, 267 Fecal transport 397 Fecal treponemes 436, 441 Feces 83, 167, 344, 378, 388, 411, 412 Feeley–Gorman Agar 202 Feeley–Gorman Agar with Selenium 202
508
Index
Feeley–Gorman Broth 203 Fermentation Base for Campylobacter 193 Fermentation Broth 201 Fermentation Medium 202 Fermentation reactions 355 F–G Agar 202 F–G Agar with Selenium 202 F–G Broth 203 FGTC Agar 203 Fildes Enrichment 490 Fildes Enrichment Agar 204 Fish Peptone Agar 204 Fish Peptone Broth 204 Fresh Yeast Extract Solution 490 Five g Agar 205 Flavobacterium meningosepticum 295 Fletcher Medium 205 Fletcher Medium with Fluorouracil 205 Fletcher’s Semisolid Medium 205 FLN Medium 205 Fluid Saboraud Medium 37 Fluid Sabouraud Medium 206 Fluid Thioglycolate Agar 206 Fluid Thioglycolate Agar with Calcium Carbonate 206 Fluid Thioglycolate Medium 206 Fluid Thioglycolate Medium with Beef Extract 207 Fluid Thioglycolate Medium with K Agar 207 Fluid Thioglycolate Medium with Rabbit Serum 207 Fluid Thioglycolate Medium, without Glucose or Eh Indicator 207 Fluorescein production 206, 208 Fluorescence Denitrification Medium 208 Fluorescence Lactose Nitrate Medium 205 Fluorocult Brilliant Green 2%-Bile Broth 84 Fluorocult Tryptose Sulfite Cycloserine Agar 457 Fluorocult TSC Agar 457 Fluorocult® E. coli 0157:H7 Agar 208 Fluorogenic procedure 187, 275 Flurouracil Leptospira Medium 205 FN Medium 208 Folic Acid Agar 208 Formate Fumarate Medium 209 FRAG Agar 209 Fragilis Agar 209 Francisella philomiragia 168, 169 Francisella tularensis 68, 168, 169, 210, 224 Francisella tularensis Isolation Medium 210 Fraser Supplement 492 Free-living amoebae 337 Freezing Medium 210 Fungi 19, 69, 74, 75, 76, 77, 81, 115, 123, 160, 162, 170, 174, 178, 182, 271, 283, 299, 300, 310, 324, 325, 343, 363, 379, 380, 381, 382, 407, 414, 417, 483 Fusarium species 39
Fusobacteria 375 Fusobacterium necrophorum 118, 211 Fusobacterium nucleatum 345 Fusobacterium pseudonecrophorum 211 Fusobacterium simiae 472 Fusobacterium species 16, 137, 138, 199, 200, 286, 345, 375 G Medium 210 GA Medium 224 GAM Agar 211 GAM Semisolid 211 Gardnerella vaginalis 117, 183, 211, 237, 301, 352, 400, 401, 468, 472 Gardnerella vaginalis Selective Medium 211 Gardnerella vaginalis Selective Supplement 492 GBNA Medium 211 GBS Agar Base, Islam 212 GBS Medium, Rapid 212 GC Agar 212, 213 GC Agar with Ampicillin 214 GC Agar with Ampicillin and Gentamicin 215 GC Agar with Ampicillin and Tetracycline 215 GC Agar with Chloramphenicol, Tetracycline, and Ampicillin 216 GC Agar with Defined Supplements 217 GC Agar with Penicillin G 217 GC Agar with Supplement A 218 GC Agar with Supplement A and with VCN Inhibitor 219 GC Agar with Supplement A and with VCTN Inhibitor 219 GC Agar with Supplement B 220 GC Medium 213 GC Medium with Chloramphenicol 223 GC Medium, New York City Formulation 221 GC Selective Supplement 492 GCA Agar with Thiamine 223 GCII Agar 221, 222 GCII Agar with Hemoglogin and IsoVitaleX® 132 GC-Lect Agar 222 Gelatin Agar 224 Gelatin Infusion Broth 224 Gelatin liquefaction 418 Gelatin liquifaction 417 Gelatin liquification 341 Gelatin Medium 225 Gelatin Metronidazole Cadmium Medium 225 Gelatin Phosphate Salt Agar 225 Gelatin Phosphate Salt Broth 226 Gelatin Salt Agar 226 Gelatin utilization 24, 225 Gelatinase 224, 225, 226 Gelatinase production 288 Gelatinase Test Medium 226
Index Gelatin-utilization 225 Gelatone 487 Gelysate peptone 487 Gemmiger formicilis 136 Genital 436 Genital treponemes 436 Genitourinary tract 301, 400, 401 Geodermatophilus obscurus 205 Germ tubes 431 Giardia cati 264 Giardia intestinalis 264 GIBCO BRL Kelly Medium, Nonselective Modified 265 Kelly Medium, Selective Modified 266 Gluconate Peptone Broth 226 Glucose Blood Liver Agar 64 Glucose fermentation 202, 355, 379, 443, 453 Glucose fermenting 256 Glucose Nutrient Agar 226 Glucose Phosphate Broth 227 Glucose Salt Teepol Broth 227 Glucose Salts Medium 227 Glucose-fermenting 85 Glutamate fermentation 147 Glutarate Medium 227 Glutarate utilization 228 Glycerol Agar 228 Glycerol Asparagine Meat Agar 228 Glycerol sensitive 291 Glycine utilization 93 GMC Medium 225 GN Broth, Hajna 228 Gonococcus Medium 229 GP Agar 229 GPHF Agar 229 GPS Agar 225 GPS Broth 226 Gram-negative anaerobes 387, 477 Gram-negative bacteria 40, 50, 119, 123, 141, 160, 190, 241, 242, 281, 296, 315, 316, 317, 335, 336, 344, 346, 347, 348, 357, 377, 384, 387, 393 Gram-negative cocci 169 Gram-negative enteric bacteria 31, 50, 160, 190, 241, 281, 315, 316, 318, 357, 363, 379 Gram-positive cocci 156, 157, 384, 403 Granada Medium 229 Group A Selective Strep Agar with Sheep Blood 230 Group A streptococci 431 Group B streptococci 446, 447 Group B Streptococci Agar 212 Group B Streptococci Medium 212 Group B Streptococcus 403 Group D-streptococci 194 GSTB 227
509
Gum Base Nalidixic Acid Medium 211 H Agar 230 H agglutination antigen 231 H Broth 231 H Diphasic Medium 232 H2S production 93, 241, 270, 275, 287, 292, 294, 317, 352, 377, 383, 393, 443 Haemophilus ducreyi 233, 234, 240, 371 Haemophilus ducreyi Medium 233 Haemophilus ducreyi Medium, Revised 233 Haemophilus Identification Quadrant Plate with Growth Factors 242 Haemophilus influenzae 117, 125, 126, 204, 214, 234, 235, 236, 321 Haemophilus influenzae Defined Medium MI 234 Haemophilus influenzae Defined Medium MI–Cit 234 Haemophilus Medium 235 Haemophilus parainfluenzae 213, 214, 215, 216, 217 Haemophilus species 32, 132, 213, 214, 219, 220, 222, 235, 242, 281 Haemophilus Test Medium 235 Haemophilus vaginalis 301, 400, 401 Ham’s F–10 Medium 236 Harlequin TBGA 451 Harpo's Htye 236 HBT Bilayer Medium 236 HC Agar 242 Heart Infusion Agar 237 Heart Infusion Agar (pH 7.6) with Inactivated Horse Serum 238 Heart Infusion Agar with 0.1% Glucose 238 Heart Infusion Agar with Glucose 238 Heart Infusion Agar with Horse Serum and Fresh Yeast Extract 238 Heart Infusion Agar with Inactivated Horse Serum 238 Heart Infusion Agar with Inactivated Horse Serum, NaCl and Penicillin 238 Heart Infusion Agar with Rabbit Blood 239 Heart Infusion Broth 239 Heart Infusion Broth (pH 7.5) with Inactivated Human Serum and Yeast Extract 239 Heart Infusion Broth with Additives for Staphylococcus 239 Heart Infusion Broth with Additives for Streptobacillus 239 Heart Infusion Broth with Inactivated Horse Serum and Fresh Yeast Extract 240 Heart Infusion Broth with Inactivated Horse Serum, Fresh Yeast Extract, and Sucrose 240 Heart Infusion Medium with Fetal Bovine Serum 240 Heart Infusion Tyrosine Agar 240 Hektoen Enteric Agar 241
510
Index
HeLa cell test 258, 260 HeLa tissue culture 122 Helicobacter Medium 241 Helicobacter nemestrinae 88 Helicobacter pylori 88, 107, 213, 214, 241, 242 Helicobacter pylori Isolation Agar 241 Helicobacter pylori Selective Medium 241 Helicobacter pylori Selective Supplement Dent 492 Helicococcus kunzii 77 Hemin Medium for Mycobacterium 308 Hemin Solution 490 Hemo ID Quad Plate 242 Hemo ID Quad Plate with Growth Factors 242 Hemoglobin 490 Hemoglobin Solution 2% 490 Hemolysis 211 Hemolytic 65, 66, 67, 237, 358, 446, 447 Hemolytic Streptococcus 404 Hemorrhagic coli Agar 242 Heparin Medium 242 Herellea Agar 242 Herellea species 242 Herpetomonas mariadeanei 282 Herpetomonas muscarum 179 Herpetomonas species 273 Hershey’s Tris–Buffered Salts Medium 243 Heterotrophic microorganisms 243, 273, 449, 451, 483, 484 Hexamita inflata 244 Hexamita Medium 243 Hexamita pusilla 244 Hexamita species 264 HiCrome Listeria Agar Base, Modified 247 HiCrome MacConkey-Sorbitol Agar 247 HiCrome MacConkey-Sorbitol Agar with Tellurite-Cefixime Supplement 248 HiCrome Enterococci Broth 247 HiCrome M-CP Agar Base 248 HiCrome MS.O157 Agar 249 HiCrome MS.O157 Agar with Tellurite 249 HiCrome Rapid Coliform Broth 249 HiCrome Rapid Enterococci Agar 250 HiCrome Salmonella Agar 250 HiCrome Salmonella Chromogen Agar 250 HiCrome UTI Agar, Modified 250 High level aminoglycoside resistant enterococci 474, 475 Hippurate Broth 395 Hippurate hydrolysis 396 Histolytic clostridia 276 Histoplasma capsulatum 74, 75, 80, 81, 252, 253, 254, 360, 380, 483 Histoplasma capsulatum Agar 251, 252 Histoplasma capsulatum Broth 253 Histoplasma duboisii 252, 254
HL Agar 254 HLARE 474, 475 Hoagland Trace Element Solution, Modified 490 Holding medium 101, 111, 115, 116, 398 HO-LE Trace Element Solution 254 Hominis Agar 230 Hominis Broth 231 Horse Blood Agar 254 Horse Blood, Citrated 490 Horse Blood, Defibrinated 490 Horse Blood, Hemolysed 490 Horse Blood, Oxalated 490 Horse Serum 490 Horse Serum Agar 255 Horse Serum Broth 255 Hoyle Medium 255 Hoyle Medium Base 255 HR Antifungal Assay Medium Buffered with MOPS 256 HTM 235 HTM Base 235 Hugh–Leifson’s Glucose Broth 256 Hugh–Leifson’s Oxidation Fermentation Medium 347 Human Blood Tween Bilayer Medium 236 Hutner’s Mineral Base 490 Hydroxybenzoate Agar 256 Hydroxybenzoate Broth 257 Hypotrichomonas species 460 IBB Agar 259 IGP Medium 260 Imidazole 116, 117 Imidazole Utilization Medium 257 Immunocompromised hosts 277 In vitro toxigenicity testing 268, 269 Indole Medium 258 Indole Nitrite Medium 258 Indole production 258, 313, 316, 393, 399, 452, 453 Indole test 258, 352 Infant botulism 146 Infection Medium 258 Infusion Agar 65 Infusion Broth 258 Inhibitory Mold Agar 259 Inositol Brilliant Green Bile Salts Agar 259 Inositol Urea Caffeic Acid Medium 259 Inositol utilization 259 Inspissation 495 International Streptomyces Project Medium 8 335 Intestinal 357, 438, 439, 441 Intestinal treponemes 438, 439, 441 Intracellular Growth Phase Medium 260 Intracellular poly-β-hydroxybutyrate production 362 Intrasporangium calvum 57 Ion Agar for Ureaplasma 260 Ionagar 487
Index Irgasan® Ticarcillin Chlorate Broth 261 Iron Agar, Lyngby 261 Iron Bacteria Isolation Medium 261 Iron Milk Medium 261 Islam GBS Agar 212 IsoVitaleX® Enrichment 490 Isobaculum melis 154 Isoleucine Hydroxamate Medium 262 Iso–Sensitest Agar 261 Iso–Sensitest Broth 262 ISP Medium 8 335 ITC Broth 261 Jones–Kendrick Pertussis Transport Medium 262 Jordan’s Tartrate Agar 263 Kanagawa reaction 475 Kanamycin Sulfate Selective Supplement 492 Kanamycin Vancomycin Blood Agar 263 Kanamycin Vancomycin Laked Blood Agar 263 Karmali’s Campylobacter Medium 110 Kasai Medium 264 KCN Broth 264 Keister's Modified TYI-S-33 Medium 264 Kelly Medium, Nonselective Modified 264 Kelly Medium, Selective Modified 265 KF Streptococcus Agar 266, 267 KF Streptococcus Broth 267 King’s OF Medium 347 Kirchner’s Enrichment Medium 267 K–L Virulence Agar 268 Klebsiella Medium 269 Klebsiella pneumoniae 193, 195, 269, 383 Klebsiella Selective Agar 269 Klebsiella species 59, 60, 98, 172, 269, 479 Klebs–Loeffler Virulence Agar 268 Kligler Iron Agar 270 Knisely Medium for Bacillus anthracis 270 Koch’s K1 Medium 270 Korthof Medium, Modified 271 Korthof’s Medium 271 Koser Citrate Medium 271 Kosmachev’s Medium 271 Kupferberg Trichomonas Base 271 Kupferberg Trichomonas Broth 272 KVBA 263 L Agar 272 L and F Basal Salts, Modified with Heptadecane 274 L Broth 272 L Diphasic Blood Agar Medium 272, 273 L Medium with Tetracycline 273 Lab-Lemco 489 Lab-Lemco Agar 273 Lactalbumin hydrolysate 488 Lactate fermentation 145 Lactobacilli 375, 376, 378, 394, 395 Lactobacillus iners 154, 155
511
Lactobacillus species 319 Lactose Broth 273 Lactose Egg Yolk Milk Agar 274 Lactose fermentation 206, 383, 409, 480 Lactose fermentation 190, 241, 276, 281, 356, 379, 409, 443, 480 Lactose Gelatin Medium 274 Lactose metabolism 344 Lash Serum Medium 274 Lauryl Sulfate Broth 275 Lauryl Sulfate Broth with MUG 275 Lauryl Tryptose Broth 275 LB Agar 275 LB Modified Broth 449 LCAT Selective Supplement 492 LD Agar 286 LD Bile Agar 286 LD Broth 286 LD Egg Yolk Agar 287 LD Esculin Agar 287 LD Gelatin Agar 287 Lead Acetate Agar 275 Lecithin Lactose Agar 276 Lecithin Lipase Anaerobic Agar 276 Lecithin Tween Medium 276 Lecithinase production 276, 287, 288, 302, 303 Legionella Agar Base 277 Legionella Agar Enrichment 490 Legionella BCYE Growth Supplement 490 Legionella BMPA Selective Supplement 492 Legionella GVPC Selective Supplement 492 Legionella Medium 277 Legionella micdadei 51 Legionella MWY Selective Supplement 492 Legionella pneumophila 51, 52, 53, 54, 55, 69, 97, 99, 202, 203, 277, 320, 322 Legionella pneumophila Medium 277 Legionella Selective Agar 277 Legionella species 51, 52, 53, 54, 55, 69, 97, 168, 277, 278, 304, 322 Leishmania aethiopica 79 Leishmania amazonensis 79 Leishmania aristedesi 79 Leishmania braziliensis 79, 178, 179, 444 Leishmania chagasi 79 Leishmania donovani 79, 179, 273, 278, 444 Leishmania enriettii 79, 178, 179 Leishmania garnhami 79 Leishmania gerbilli 79 Leishmania guyanensis 79 Leishmania hertigi 79, 278 Leishmania infantum 79 Leishmania major 79 Leishmania Medium 278 Leishmania mexicana 79
512
Index
Leishmania panamensis 79 Leishmania pifanoi 79 Leishmania species 67, 337 Leishmania tarentolae 179 Leishmania tropica 79, 178, 179, 278 LEMB Agar 281 Leptospira Enrichment 490 Leptospira Medium 278 Leptospira Medium, Ellinghausen–McCullough/ Johnson–Harris 278 Leptospira Medium, EMJH 278 Leptospira Medium, Modified 279 Leptospira PF Medium 279 Leptospira Protein–Free Medium 279 Leptospira species 72, 73, 74, 205, 271, 278, 279, 372, 405 Leptotrichia buccalis 206, 264, 280, 472 Leptotrichia buccalis Medium 279 Leptotrichia Medium 280 Letheen Agar 280 Letheen Agar, Modified 280 Letheen Broth 281 Letheen Broth, Modified 281 Levine EMB Agar 281 Levine Eosin Methylene Blue Agar 281 Levinthal’s Agar 281 L-forms 99 Lipase activity 146, 393 Lipase production 276, 288, 302, 303 Listeria Enrichment Broth 281 Listeria Fermentation Broth 282 Listeria HiCrome Agar Base, Modified 247 Listeria ivanovii 142 Listeria monocytogenes 59, 60, 62, 142, 194, 212, 247, 254, 282, 292, 300, 317, 346, 350, 449, 468 Listeria Primary Selective Enrichment Supplement 492 Listeria Selective Agar, Modified Oxford 346 Listeria Selective Agar, Oxford 346 Listeria Selective Enrichment Supplement 492 Listeria Selective Supplement MOX 492 Listeria Selective Supplement Oxford 493 Listeria species 98, 172, 282, 350, 373, 444 Listeria Transport Enrichment Medium 282 LIT Medium 282 Lithium Chloride Phenylethanol Moxalactam Plating Agar 291 Litmus Milk 282 Littman Oxgall Agar 283 Liver Broth 283 Liver digest neutralized 488 Liver Infusion Agar 283 Liver Infusion Broth 283 Liver Veal Agar 283 Liver Veal Egg Yolk Agar 284 Loeffler Blood Serum Medium 284, 285
Loeffler Medium 285 Loeffler Slant 285 Loeffler Slant, Modified 285 LOM Agar 294 Lombard–Dowell Agar 286 Lombard–Dowell Bile Agar 286 Lombard–Dowell Broth 286 Lombard–Dowell Egg Yolk Agar 287 Lombard–Dowell Esculin Agar 287 Lombard–Dowell Gelatin Agar 287 Lombard–Dowell Neomycin Agar 288 Long–Term Preservation Medium 288 Low Iron YC Agar 289 Low Iron YC Broth 289 Lowenstein–Gruft Medium 290 Lowenstein–Jensen Medium 290, 291 Lowenstein–Jensen Medium with NaCl 291 Lowenstein–Jensen Medium without Glycerol 291 LPM Agar 291 LPM Agar with Esculin and Ferric Iron 292 LST-MUG Broth 292 LT Medium 276 Lyngby Iron Agar 261 Lysine Arginine Iron Agar 292 Lysine Broth Falkow with NaCl 293 Lysine deaminase 313 Lysine decarboxylase 293, 294, 313, 377 Lysine Decarboxylase Broth, Falkow 293 Lysine Decarboxylase Broth, Taylor Modification 293 Lysine Decarboxylase Medium 293 Lysine Iron Aga 293 Lysine Ornithine Mannitol Agar 294 Lysine-decarboxylase 480 M7 Medium 294 M9 Medium with Casamino Acids 295 MacConkey Agar 295 MacConkey Agar No. 2 296 MacConkey Agar No. 3 296 MacConkey Agar with Sorbitol 396 MacConkey Agar without Crystal Violet 296 MacConkey Agar without Salt 297 MacConkey Agar, CS 296 MacConkey II Agar 296 MacConkey MUG Agar 297 MacConkey-Sorbitol Agar, HiCrome 247 Macrospore 343 Magnesium Oxalate Agar 297 Maintenance of L Antigen in Neisseria 297 Malachite Green Broth 298 Malassezia species 180 Malonate Broth 298 Malonate Broth, Ewing Modified 298 Malonate utilization 357 Malt Agar 298 Malt extract 489
Index Mammalian cells 379, 428, 429 Mannitol Egg Yolk Polymyxin Agar 298 Mannitol fermentation 121, 144, 151, 196, 202, 294, 356, 453 Mannitol Salt Agar 298 Martin–Lewis Agar 299 Martin–Lewis Agar, Enriched 299 Mastigamoeba invertens 244 Maximum Recovery Diluent 300 M-Bismuth Sulfite Broth 64 MBM Medium 304 McBride Listeria Agar 300 McCarthy Agar 300 McClung Carbon–Free Broth 301 McClung Toabe Agar 301 McClung–Toabe Agar, Modified 301, 302 McClung–Toabe Egg Yolk Agar, CDC Modified 302 McCoy cells 186 M-CP HiCrome Agar Base 248 M-CP Medium 303 Medium for Ureaplasma 44 MEM with Earle’s Salts and Nonessential Amino Acids 186 Membrane Clostridium perfringens HiCrome Agar Base 248 Membrane filter method 64, 191, 192, 269, 275, 399, 411, 412 Membrane Lactose Glucuronide Agar 303 M-Endo Agar, LES 191 M-Endo Broth 192 Meningococci 75, 455 M-Enterococcus Agar 194 Mercurial preservatives 419 MES Agar 461 Metabolic 25 Metabolism of carbohydrates 346, 347, 348 Methyl Red test 319 Methyl Red– Voges–Proskauer Broth 319 Methyl Red Voges–Proskauer Medium 319 Methylene Blue Milk Medium 304 M–Fecal Coliform Agar, Modified 201 MH IH Agar 304 MIC testing 478 Microaerophiles 10, 418, 419 Microaerophilic 82, 83, 206, 207, 420 Microaerophilic microorganisms 29 Micrococcus luteus 332, 340 Micrococcus species 202 Micromonospora purpurea 56 Micromonospora species 229 Microspora species 42, 157, 271, 341 Microtetraspora fusca 229 Microtetraspora helvata 56 Middlebrook 13A Medium 304
513
Middlebrook 7H10 Agar with Middlebrook ADC Enrichment 307 Middlebrook 7H10 Agar with Middlebrook OADC Enrichment 307 Middlebrook 7H10 Agar with Middlebrook OADC Enrichment and Hemin 308 Middlebrook 7H10 Agar with Middlebrook OADC Enrichment and Triton WR 1339 308 Middlebrook 7H10 Agar with Streptomycin 309 Middlebrook 7H11 Agar with Middlebrook ADC Enrichment 310 Middlebrook 7H11 Agar with Middlebrook OADC Enrichment 310 Middlebrook 7H11 Agar with Middlebrook OADC Enrichment and Triton WR 1339 311 Middlebrook 7H11 Agar, Selective 309 Middlebrook 7H12 Medium 311 Middlebrook 7H9 Broth with Middlebrook ADC Enrichment 305 Middlebrook 7H9 Broth with Middlebrook OADC Enrichment 305 Middlebrook 7H9 Broth with Middlebrook OADC Enrichment and Triton WR 1339 306 Middlebrook 7H9 Broth, Supplemented 305, 306 Middlebrook ADC Enrichment 305, 490 Middlebrook Albumin Dextrose Catalase Enrichment 305 Middlebrook and Cohn 7H10 Agar 307 Middlebrook Medium 312 Middlebrook Medium with Mycobactin 312 Middlebrook OADC Enrichment 313, 490 Middlebrook OADC Enrichment with Triton WR 1339 313 Middlebrook Oleic Albumin Dextrose Catalase Enrichment 313 Middlebrook Oleic Albumin Dextrose Catalase Enrichment with Triton WR 1339 313 MIL Medium 313 Milk carbohydrate fermentation 261 Minimum Essential Medium with Bicarbonate, Serum, and Antibiotics 313 MIO Medium 316 Mitis–Salivarius Agar 314 M-Lauryl Sulfate Broth 275 M–LES, Endo Agar 191 MLGA 303 Modified Oxford Antimicrobic Supplement 493 Modified Thayer–Martin Agar 413, 415 Molds 16, 37, 75, 79, 81, 115, 206, 363, 382 Møller Decarboxylase Broth 315 Molybdate Agar 315 Monkey kidney cells 337 Monsur Agar 315 Moraxella bovis 107 Moraxella catarrhalis 58
514
Index
Moraxella lacunata 285 Moraxella lincolnii 101 Moraxella nonliquefaciens 107, 213, 214 Moraxella osloensis 107, 320 Moraxella urethralis 58 Morococcus cerebrosis 214 Motile phase 316 Motility 49, 166, 187, 313, 316, 317, 318, 389, 393, 445 Motility GI Medium 315 Motility Indole Lysine Medium 313 Motility Indole Ornithine Medium 316 Motility Medium S 316 Motility Nitrate Agar 316 Motility Nitrate Medium 316, 317 Motility Nitrate Medium, Buffered 317 Motility Sulfide Medium 317 Motility Test and Maintenance Medium 317 Motility Test and Maintenance Medium, Gilardi 318 Motility Test and Maintenance Medium, Tatum 318 Motility Test Medium 318 Motility Test Medium, Semisolid 318 Mouse adrenal assay 236 MOX Agar 297, 346 MRS Agar 319 MRS Broth 319 MRVP Broth 319 MRVP Medium 319 MS.O157 Agar HiCrome 249 MS.O157 Agar with Tellurite, HiCrome 249 MSRV Selective Supplement 493 M–ST Holding Medium 398 M–Staphylococcus Broth 399 M–Tetrathionate Broth 411 MTM II 413 M–TT Broth 411 Mucate Broth 319 Mucate Control Broth 320 Mucor hiemalis 80 Mueller Hinton Agar 320 Mueller Hinton Broth 320 Mueller Hinton Chocolate Agar 321 Mueller-Hinton Agar with IsoVitaleX® and Hemoglobin 320 Mueller-Hinton II Agar 321 Mueller-Hinton Medium with Garden Soil 321 MUG Tryptone Soya Agar 321 Muller-Kauffmann Tetrathionate Broth 321 Multiple tube technique 354 Multiple-tube fermentation technique 275 Multiple-Tube Technique 44 MWY Medium 322 Mycelial phase 253 Mycin Assay Agar 322 Mycobacteremia patients 305, 312
Mycobacteria 344 Mycobacteria 7H11 Agar with Middlebrook ADC Enrichment 310 Mycobacteria 7H11 Agar with Middlebrook OADC Enrichment 310 Mycobacteria 7H11 Agar with Middlebrook OADC Enrichment and Triton WR 1339 311 Mycobacterium Agar 322 Mycobacterium avium 290, 291, 307, 323, 352 Mycobacterium avium subsp. paratuberculosis 313 Mycobacterium bovis 291, 402, 407, 408 Mycobacterium chelonae 40 Mycobacterium diernhoferi 57 Mycobacterium fortuitum 40 Mycobacterium gastri 352 Mycobacterium gordonae 290, 291 Mycobacterium haemophilum 308 Mycobacterium kansasii 290, 291, 309, 352 Mycobacterium leprae 41, 475 Mycobacterium paratuberculosis 323 Mycobacterium scrofulaceum 352 Mycobacterium smegmatis 229, 290, 291 Mycobacterium species 40, 41, 57, 181, 229, 267, 305, 306, 307, 308, 309, 312, 313, 322, 324, 343, 353, 371, 392, 407, 408, 458, 475 Mycobacterium terrae 352 Mycobacterium tuberculosis 15, 40, 41, 152, 153, 290, 291, 305, 306, 307, 308, 309, 310, 311, 385, 407, 408 Mycobacterum species 290, 291 Mycobactin Medium 322 Mycobactosel Agar 323 Mycobactosel L–J Medium 324 Mycobiotic Agar 324 Mycological Agar 324 Mycological Agar with Low pH 324 Mycological Broth 325 Mycological peptone 488 Mycophil Broth 325 Mycoplasma 326, 462, 463, 464 Mycoplasma Agar 325 Mycoplasma Agar Base 326 Mycoplasma Agar with Increased Selectivity 326 Mycoplasma Agar with Supplement G 326 Mycoplasma Agar with Supplement P 327 Mycoplasma Broth 327 Mycoplasma Broth Base 328 Mycoplasma Broth with Supplement G 328 Mycoplasma Broth with Supplement P 329 Mycoplasma Broth, Supplemented 328 Mycoplasma Enrichment without Penicillin 490 Mycoplasma hominis 231, 232 Mycoplasma Horse Serum Broth 329 Mycoplasma pneumoniae 231, 233, 330, 334, 335 Mycoplasma pneumoniae Isolation Medium 329
Index Mycoplasma species 42, 43, 99, 240, 326, 327, 328, 329, 363, 364, 397 Mycoplasma Supplement 490 Mycoplasma Supplement G 493 Mycoplasma Supplement P 493 Mycoplasma Supplement S 493 Mycoplasmal Agar 330 Mycoplasmas 166 Mycoplasmatales 334, 335 Nadi reaction 18 Naegleria australiensis 385 Naegleria fowleri 295, 314, 331, 385 Naegleria gruberi 295 Neisseria animalis 176 Neisseria gonorrhoeae 25, 117, 155, 158, 176, 217, 218, 219, 220, 221, 223, 229, 243, 298, 321, 417, 436 Neisseria lactamica 239 Neisseria Medium 330 Neisseria meningitidis 117, 158, 320, 321, 330, 417 Neisseria meningitidis Medium 330 Neisseria species 63, 131, 132, 158, 166, 213, 214, 219, 220, 221, 222, 299, 300, 320, 330, 334, 335, 365, 366, 373, 405, 406, 414, 415, 416, 417, 434, 435 Nelson Medium for Naegleria fowleri 331 Nelson's Culture Medium for Naegleria 330, 331 Neomycin Agar, Modified 331 Neomycin Assay Agar 36 Neomycin Blood Agar 331 Neomycin Luria Agar 332 Neomycin Medium No. 1 332 Neopeptone Glucose Agar 332 Neopeptone Glucose Rose Bengal Aureomycin® Agar 332 Neopeptone Infusion Agar 333 Neufeld (Quellung) reaction 479 New York City Medium 333 New York City Medium, Modified 334 Newborn infants 360, 361 Nickerson Medium 59 Niger Seed Agar 63 NIH Agar 335 NIH Thioglycolate Broth 335 Nitrate Agar 335 Nitrate assimilation 476 Nitrate Broth 335, 336 Nitrate Broth, Campylobacter 336 Nitrate reduction 93, 258, 316, 317, 335, 336, 337, 407, 444 Nitrate Reduction Broth 336 Nitrate Reduction Broth for Pseudomonas and Related Genera 337 Nitrate Reduction Broth, Clark 336 Nitrogen source 170, 171, 259, 298
515
Nitsch’s Trace Elements 490 NNN Medium 337 Noble agar 487 Nocardia asteroides 57, 225 Nocardia brasiliensis 225 Nocardia brevicatena 57 Nocardia calcarea 57 Nocardia farcinica 322 Nocardia histidans Medium 337 Nocardia otitidiscaviarum 57 Nocardia paucivorans 154 Nocardia salmonicolor 56 Nocardia species 57, 133, 225, 291, 479 Nocardia transvalensis 40 Nonfat Dry Milk, Reconstituted 337 Nonfermenting Gram-negative bacteria 13, 140, 465 Nonnutrient Agar Plates 337 Non-sporeforming anaerobes 166 Nonsporulating anaerobes 478 NOS Medium, Modified 337 NOS Spirochete Medium 338 Nose 451 Nosema corneum 314 Novobiocin Agar 338 Novy, MacNeal and Nicole Medium 337 Nuclearia species 295 Nutrient 340 Nutrient Agar 339 Nutrient Agar No.2 339 Nutrient Agar with 0.5% NaCl 340 Nutrient Agar with 2% NaCl 340 Nutrient Agar with Dihydrostreptomycin 339 Nutrient Agar with Erythromycin 340 Nutrient Agar with Formate, Fumarate, and Horse Blood 339 Nutrient Agar with Horse Serum 340 Nutrient Agar with Yeast Extract 340 Nutrient Broth 340, 341 Nutrient Broth No. 2 341 Nutrient Broth, Standard II 341 Nutrient Gelatin 341 Nystatin Assay Agar 37 N–Z Amine A Medium with Soluble Starch and Glucose 341 N-Z-Amine Glycerol Agar 341 NZY Agar 342 NZY Broth 342 O157:H7 ID Agar 342 O157:H7(+) Plating Medium 342 OA 343 Oatmeal Agar 343 Obligate anaerobes 419, 421 Octosporomyces octosporus 479 OF Glucose Medium, Semisolid 348 OF Glucose Medium, Semisolid with NaCl 348
516
Index
OF Medium 346, 347 OF Test Medium 348 Ogawa TB Medium 343 Oleic Albumin Complex 343, 490 Oligella ureolytica 214 Oligella urethralis 58, 214 Olinella succinogenes 138 Önöz Salmonella Agar 343 ONPG Broth 344 Onsporulating anaerobes 477 OR Indicator Agar 344 Oral 436, 437, 438, 439 Oral cavity 375 Oral Fusobacterium Medium 344 Oral Treponema Medium 345 Oral treponemes 436, 437, 438, 439 Organic Acid Medium KP 345 Organic Acid Medium, Kauffmann and Petersen 345 Ornithine Broth 345 Ornithine Broth with NaCl 345 Ornithine decarboxylase 171, 294, 315, 316, 343, 377, 389 Oxford Antimicrobic Supplement 493 Oxford Agar 346 Oxford Agar, Modified 346 Oxgall 493 Oxidation–Fermentation Medium 346 Oxidation-Fermentation Medium, Hugh–Leifson’s 347 Oxidation-Fermentation Medium, King’s 347 Oxidation–Reduction Indicator Agar 344 Oxidative-Fermentative Glucose Medium, Semisolid 348 Oxidative-Fermentative Glucose Medium, Semisolid, with NaCl 348 Oxidative-Fermentative Medium 347 Oxidative–Fermentative Test Medium 348 Oxytetracycline GYE Supplement 493 P Agar 348 Packer’s Agar 43 Paenibacillus spp. 155 Pagano Levin Agar 348 Pai Medium 349 PALCAM Agar 349 PALCAM Selective Supplement 493 Paracoccidioides brasiliensis 80 Paratetramitus jugosus 331 Paratyphoid 357 Paromomycin Vancomycin Blood Agar 369 Pasteurella haemolytica 107, 350 Pasteurella haemolytica Selective Medium 350 Pasteurella multocida 107, 350, 485 Pasteurella multocida Selective Medium 350 Pasteurella species 450 Pasteurella volantium 214
PDM-114 Medium 350 PDY Agar 363 Pectinatus frisingensis 472 Pediococcus acidilactici 124 Pediococcus halophilus 80 Pediococcus species 211 Penassay Base Agar 34 Penassay Broth 34 Penassay Seed Agar 34 Penicillium 170 Penicillium species 163 Peptamin 487 Peptococcus species 387 Peptone Glycerol Phosphate Broth 354 Peptone Iron Agar 351 Peptone Meat Extract Soil Extract Agar 352 Peptone Starch Dextrose Agar 352 Peptone Water 352 Peptone Water with Andrade’s Indicator 352 Peptone Yeast Trypticase Agar 353 Peptones 487 Peptonized Milk Agar 353 Peptostreptococcus anaerobius 472 Peptostreptococcus asaccharolyticus 472 Peptostreptococcus hydrogenalis 211 Peptostreptococcus indolicus 472 Peptostreptococcus magnus 160, 162, 472 Peptostreptococcus micros 472 Peptostreptococcus prevotii 472 Peptostreptococcus species 138, 387 Peptostreptococcus tetradius 211, 472 Perfringens Agar, OPSP 150 Perfringens OPSP Selective Supplement A 493 Perfringens SFP Selective Supplement A 493 Perfringens TSC Selective Supplement A 493 Petragnani Medium 353 Pfizer Selective Enterococcus Agar 353 PGA 354 PGP Broth 354 PGS Agar 354 PGT Medium 354 pH buffers 494 pH indicators 494 PHB Medium 362 Phenol coefficients 38 Phenol Red Agar 354, 355 Phenol Red Broth 355 Phenol Red Glucose Broth 355 Phenol Red Lactose Agar 355 Phenol Red Lactose Broth 356 Phenol Red Mannitol Agar 356 Phenol Red Mannitol Broth 356 Phenol Red Sucrose Broth 356 Phenol Red Tartrate Agar 357 Phenol Red Tartrate Broth 357
Index Phenylalanine Agar 357 Phenylalanine Deaminase Medium 357 Phenylalanine Malonate Broth 357 Phenylalanine production 357 Phenylethanol Agar 357 Phenylethanol Blood Agar 358 Phenylketonuria 360, 361 Phenylketonuria Test Agar 360 PHYG Medium 358 Phytone peptone 488 Pigment production 285, 366, 367 Pike Streptococcal Broth 358 Pine and Drouhet’s Histoplasma Yeast Phase Medium 358 Pisu Medium 360 PKU 360, 361 PKU Test Agar 360 Plaque 264 Plate Count MUG Agar 361 Pleisomonas Differential Agar 259 Plesiomonas species 259, 384 PLET Agar 361 Pneumococci 67, 75, 166, 455 Pneumonia 363, 364 Poly-b-Hydroxybutyrate Medium 362 Polymyxin Acriflavine LiCl Ceftazidime Esculin Mannitol Agar 349 Polymyxin Base Agar 36 Polymyxin Seed Agar 36 Polymyxin Staphylococcus Medium 362 Polypeptone 488 Porcine Heart Agar 362 Porphyromonas species 138 Potassium Cyanide Broth 362 Potassium Tellurite Agar 363 Potato Dextrose Yeast Agar 363 Potato Extract Agar 363 Potato-Glucose Agar 354 PPLO Agar 363 PPLO Agar Base 326 PPLO Broth Base without Crystal Violet 328 PPLO Broth with Crystal Violet 364 PPLO Broth without Crystal Violet 364 PPLO Broth without Crystal Violet with Horse Serum and Fresh Yeast Extract 364 PPLO Serum Fraction 491 PPLOs 364 Preparation of Media 494 Preston Blood–Free Medium 103 Preston’s Campylobacter Medium 110 Presumpto Media 364 Pressure–temperauture relationships 494 Prevotella species 138 Propionibacterium acnes 472 Propionibacterium avidum 472
517
Propionibacterium granulosum 472 Propionibacterium lymphophilum 472 Propionibacterium propionicus 58 Propionibacterium species 16, 138, 483 Prosthetic valve endocarditis 277 Proteolytic ability 287, 288, 303 Proteolytic activity 394, 396 Proteolytic microorganisms 224 Proteose No. 3 Agar 365, 366 Proteose Peptone 487, 488 Proteose peptone No. 2 488 Proteose peptone No. 3 488 Proteose Yeast Extract Medium 366 Proteus mirabilis 214 Proteus species 83, 172, 251, 297, 362, 363, 383, 412, 465 Proteus vulgaris 283 Providencia species 480 PSD Agar 352 PSE Agar 353 Pseudomonadaceae 336, 337 Pseudomonads 206 Pseudomonas 444 Pseudomonas aeruginosa 11, 12, 13, 40, 55, 98, 123, 206, 208, 255, 283, 298, 332, 340, 366, 367, 395 Pseudomonas Agar F 366 Pseudomonas Agar P 366 Pseudomonas alcaligenes 12 Pseudomonas Basal Mineral Medium 367 Pseudomonas cepacia 12, 206, 344 Pseudomonas CFC Agar 367 Pseudomonas chlorotidismutans Medium 367 Pseudomonas CN Agar 367 Pseudomonas denitrificans 206, 208 Pseudomonas fluorescens 12 Pseudomonas maltophila 344 Pseudomonas mendocina 206, 208 Pseudomonas pertucinogena 71 Pseudomonas putida 12 Pseudomonas species 11, 83, 99, 114, 172, 209, 226, 238, 258, 362, 367, 368, 458 Pseudomonas species. 164 Pseudonocardia thermophila 57 Pseudosel® Agar 123 Purine fermenting 147 Purple Agar 368 Purple Broth 368 Purple Carbohydrate Broth 368 Purple Lactose Agar 369 Purple Serum Agar Base 369 PV Blood Agar 369 PY Basal Medium 369 Pyrazinamidase Agar 370 Pyrazinamidase production 370
518
Index
Pyrazinamide Medium 370 Pyruvate metabolization 370 Pyruvate Utilization Medium 370 Pyruvic Acid Egg Medium 370 Quaternary ammonium compounds 281 R Medium 371 Rabbit Blood Agar 371 Rabbit Blood, Citrated 491 Rabbit Blood, Defibrinated 491 Rabbit Heart Infusion Agar 371 Rabbit Serum Bovine Serum Albumin Tween 80 Medium 371 Rabbit Serum BSA Tween 80 Medium 371 Rabbit Serum Medium 371 Rainbow Agar O157 372 Rambach Equivalent Agar 250, 382 RAMBACH® Agar 372 Rap Broth, Modified 373 Rapid Coliform HiCrome Broth 249 Rapid Enterococci HiCrome Agar 250 Rapid Fermentation Medium 373 RAPID´E. coli 2 Agar 373 RAPID´Enterococcus Agar 373 RAPID´L. mono Medium 373 Rappaport Broth, Modified 373 Rappaport–Vassiliadis Enrichment Broth 374 Rappaport–Vassiliadis R10 Broth 374 Rappaport–Vassiliadis Soya Peptone Broth 374 Reactivation with Tryptone Soya Broth 374 Rectal swabs 87, 91 Reduced Transport Fluid 375 Regan–Lowe Charcoal Agar 375 Regan–Lowe Medium 375 Regan–Lowe Semisolid Transport Medium 375 Reinforced Clostridial Agar 376 Reinforced Clostridial Medium 376 Reinforced Clostridial Medium with Sodium Lactate 376 Replicate plating technique 447 Rhodococcus species 57, 291 Rice Extract Agar 376, 377 Rice Infusion Oxgall Tween 80 Agar 377 Rimler–Shotts Medium 377 RIOT Agar 377 Rogosa Agar 377 Rogosa Selective Lactobacillus Agar 378 Rogosa Selective Lactobacillus Broth 378 Rogosa SL Agar 378 Rogosa SL Broth 378 RPF Supplement 491 RPMI 1640 Medium with L-Glutamine 378 RS Medium 377 Russell Double-Sugar Agar 379 RV Enrichment Broth 374 RVS Broth 374
Ryan’s Aeromonas Medium 18 SABHI® Agar 379 SABHI Agar, Modified 380 SABHI Blood Agar 380 Sabouraud Agar 380 Sabouraud Agar with CCG and 3% NaCl 380 Sabouraud Agar with CCG and 5% NaCl 381 Sabouraud Agar, Diluted 1/10 381 Sabouraud Glucose Agar, Emmons 381 Sabouraud Glucose and Brain Heart Infusion Agar 379 Sabouraud Glucose Broth 381 Sabouraud Liquid Broth, Modified 37 Sabouraud Maltose Agar 381 Sabouraud Maltose Broth 382 Sabouraud Medium, Fluid 382 Saccaromyces cerevisiae 315 Saccharomyces species 479 Saccharopolyspora rectivirgula 57 Saliva 264, 378, 394, 395 Salmonella 293, 297, 357, 382, 383, 410, 413 Salmonella Agar, HiCrome 250 Salmonella Chromogen Agar 382 Salmonella Chromogen Agar, HiCrome 250 Salmonella Chromogenic Agar 382 Salmonella enteritidis 263 Salmonella paratyphi 388 Salmonella paratyphi A 263 Salmonella Rapid Test Elective Medium 383 Salmonella Rapid Test Elective Medium, 2X 383 Salmonella Shigella Agar, Modified 383 Salmonella species 50, 57, 64, 83, 84, 98, 141, 143, 171, 172, 173, 174, 228, 231, 241, 250, 263, 273, 296, 318, 322, 337, 344, 349, 363, 372, 374, 382, 383, 385, 388, 411, 412, 445, 478, 481 Salmonella typhi 57, 63, 64, 83, 349, 388, 410, 411, 412, 478 Salmonella–Shigella Agar 383 Salmonella–Shigella Deoxycholate Agar 397 Salt Meat Broth 383 Salt tolerance 384, 395 Salt Tolerance Medium 384 Salt Tolerance Medium, Gilardi 384 Salt Tolerance Medium, Tatum 384 Sauton’s Medium 385 SBG Enrichment Broth 385 SBG Sulfa Enrichment 385 SCGYEM Medium 385 Schaedler Agar 385, 386 Schaedler Agar with Vitamin K1 and Sheep Blood 386 Schaedler Anaerobic Agar 385 Schaedler Anaerobic Broth 386 Schaedler Broth 386 Schaedler CNA Agar with Vitamin K1 and Sheep Blood 386
Index Schaedler KV Agar with Vitamin K1 and Sheep Blood 387 Schizophyllum Medium 387 Schleifer–Krämer Agar 387 SD Medium 389 Seed Agar 34 Selective 7H11 Agar 392 Selective Components 491 Selenite Brilliant Green Enrichment Broth 385 Selenite Broth 387 Selenite Broth Base, Mannitol 388 Selenite Broth, Lactose 387 Selenite Cystine Broth 388 Selenite F Broth 388 Selenite F Enrichment Medium 387 Selenomonas noxia 136 Selenomonas species 138 Semiselective Medium for Legionella pneumophila 69 Semisolid Brucella Broth 388 Semisolid BSA Tween 80 Medium 74 Semisolid Medium for Motility 388 Sensitest Agar 389 Sensitivity assays 389 Sensitivity testing 177 Serological identification 431 Serological typing 431 Serratia Differential Medium 389 Serratia Hd–MHr 389 Serratia liquefaciens 389 Serratia marcescens 55, 79, 181, 262, 354, 389, 390, 449, 450 Serratia Medium 390 Serratia species 27, 59, 60, 165, 182, 389, 413 Serum Glucose Agar 390 Serum Glucose Agar, Farrell Modified 390 Serum Potato Infusion Agar 391 Serum Tellurite Agar 391 Seven H11 Agar 392 SF Broth 392 Sheep Blood, Citrated 491 Sheep Blood, Defibrinated 491 Shepard’s Differential Agar 6 Shepard’s M10 Medium 398 Shigella 297 Shigella Broth 392 Shigella dysenteriae 340 Shigella flexneri 340 Shigella species 13, 50, 158, 171, 172, 173, 174, 228, 241, 296, 319, 320, 340, 363, 383, 393, 480, 481 Shiitake Agar 393 Sierra Medium 393 SIM Medium 393 Simmons’ Citrate Agar 393
519
Simmons’ Citrate Agar, Modified 13 SK Agar 387 Skim Milk Agar 394 Skin 174, 197 Skirrow Brucella Medium 394 Skirrow’s Campylobacter Agar 102 SLA Trace Elements 491 Snyder Agar 394 Snyder Test Agar 394 Sodium Acetate Agar 13 Sodium Biselenite Medium 387 Sodium Chloride Broth, 6.5% 395 Sodium Chloride SUC Medium 900 395 Sodium Chloride Sucrose Medium 900 395 Sodium Chloride Sucrose Medium 900 with Penicillin G 395 Sodium Desoxycholate 493 Sodium Hippurate Broth 395 Sodium Hydrogen Selenite Medium 387 Sodium Taurocholate 493 Soft Agar Gelatin Overlay 396 Solution sterility 419 Sorbitol MacConkey Agar 396 Soy Peptone Broth 397 Soya peptone 488 Soybean Casein Digest Agar 446 Soytone 487 Special peptone 488 Specimen Preservative Medium 397 Spinal fluid 175 Spirochaeta species 94 Spirochetes 265 Sporothrix schenckii 80 Sporulation 18 Sporulation Medium, Modified 182 Spray’s Fermentation Medium 397 Sprotrichum schenckii 252, 254 SPS Agar 397 SS Agar 383 SS Agar, Modified 383 SS Deoxycholate Agar 397 SSDC 397 ST Holding Medium 398 STAA Selective Supplement 493 Staib Agar 63 Standard Fluid Medium 10B 398 Standard II Nutrient Agar 399 Stanier’s Basal Medium with Pyridoxine and Yeast Extract 399 Staph/Strep Selective Supplement 493 Staphylococcal enterotoxin 76 Staphylococcal food poisoning 384 Staphylococci 43, 47, 48, 65, 96, 125, 194, 197, 297, 299, 358, 384, 399, 409, 433 Staphylococcus Agar No. 110 399
520
Index
Staphylococcus aureus 35, 48, 118, 141, 151, 164, 196, 197, 237, 339, 362, 399, 400, 432, 450, 453, 473 Staphylococcus Broth 399 Staphylococcus Medium 399 Staphylococcus Medium No. 110 399 Staphylococcus species 44, 98, 151, 165, 180, 181, 189, 202, 239, 348, 387, 400 Staphylococcus–Streptococcus Selective Medium 400 Starch Agar 400 Starch Agar with Bromcresol Purple 400, 401 Starch hydrolysis 204, 400, 401 Starch Hydrolysis Agar 401 Sterility Test Broth 401 Sterility testing 10, 82, 83, 206, 207, 335, 401, 418, 420, 421 Stock Culture Agar 401 Stock Culture Agar with L-Asparagine 402 Stonebrink’s Medium 402 Stool specimens 397 Strep (Streptococcus) ID (Identification) Quad Plate 403 Strep ID Quad Plate 402 StrepB Carrot Broth 403 Streptobacillus moniliformis 239, 240, 255 Streptobacillus species 240 Streptococcal Growth Medium 403 Streptococci 29, 43, 47, 59, 60, 65, 66, 67, 75, 140, 166, 194, 195, 196, 212, 230, 267, 304, 332, 358, 375, 400, 402, 403, 404, 405, 431, 453, 454, 455, 465, 469 Streptococcus Agar 403 Streptococcus agalactiae 332, 446, 447 Streptococcus Blood Agar, Selective 403 Streptococcus bovis 203 Streptococcus dysgalactiae 155 Streptococcus equinus 204 Streptococcus faecalis 392, 413 Streptococcus faecalis Broth 392 Streptococcus faecium 392 Streptococcus iniae 57 Streptococcus Medium 404 Streptococcus mitis 315 Streptococcus mutans 375 Streptococcus pneumoniae 43, 154, 321, 404, 448 Streptococcus pneumoniae Medium 404 Streptococcus pyogenes 57, 80, 230, 332, 469 Streptococcus salivarius 315 Streptococcus sanguis 375 Streptococcus Selective Medium 404 Streptococcus Selective Supplement COA 493 Streptococcus species 44, 206, 304, 384, 392, 403, 404, 413, 472 Streptomyces flocculus 57
Streptomyces species 56, 58, 116, 225, 228, 479 Streptomyces thermoautotrophicus 17 Streptomyces yerevanensis 229 Streptomycin 422 Streptomycin Assay Agar with Yeast Extract 35 Streptosel Agar 404 Streptosel Broth 405 STT Agar 406 Stuart Leptospira Broth, Modified 405 Stuart Medium Base 405 Stuart Transport Medium 405 Stuart Transport Medium, Modified 405 Sucrose fermentation 241, 356, 406, 443, 480 Sucrose Phosphate Glutamate Transport Medium 406 Sucrose Phosphate Transport Medium 406 Sucrose Teepol Tellurite Agar 406 Sucrose Yeast Extract Medium 406 Sudan Black B 362 Sugar fermentation 270 Sulfamandelate Supplement 493 Sulfite Polymyxin Sulfadiazine Agar 397 Sulfonamide therapy 80, 81 Sulfonamides 38, 422 Supplement A 491 Supplement B 491 Supplement C 491 Supplement VX 491 Swab specimens 25, 436 T1N0 Broth 429 T1N1 Agar 430 T1N1 Broth 430 T1N2 Agar 430 T1N3 Broth 430 T1N6 Broth 430 T1N8 Broth 430 T1N10 Broth 430 Tap Water Agar 407 Tarshis Blood Agar 407 Tartrate fermentation 357 Taurocholate Tellurite Gelatin Agar 315 Taylorella equigenitalis 214 TB Nitrate Reduction Broth 407 TBX Agar 407 TC Amino Acids, HeLa 100X 422 TC Amino Acids, Minimal Eagle 50X 422 TC Dulbecco Solution 423 TC Earle Solution 423 TC Hanks Solution 423 TC Medium 199 423 TC Medium Eagle with Earle BSS 424 TC Medium Eagle with Hanks BSS 424 TC Medium Eagle, HeLa 425 TC Medium Ham F10 425 TC Medium NCTC 109 426 TC Medium RPMI #1640 427
Index TC Minimal Medium Eagle Spinner Modified MEM–S 429 TC Minimal Medium Eagle with Earle BSS 428 TC Tyrode Solution 429 TC Vitamins Minimal Eagle, 100X 429 TCBS Agar 407 TCH Medium 408 Tellurite Blood Agar 132 Tellurite Glycine Agar 408, 409 Tellurite Polymyxin Egg Yolk Agar 432 Tellurite Solution 493 Tergitol 7 Agar 409 Tergitol 7 Agar H 410 Tergitol 7 Broth 410 Tetrathionate Broth 410, 411 Tetrathionate Broth with Novobiocin 412 Tetrathionate Broth, Hajna 412 Tetrathionate Broth, USA 412 Tetrathionate Crystal Violet Enhancement Broth 412 Tetrathionate Reductase Test Medium 413 Tetrathionate reduction 413 Tetrazolium Thallium Glucose Agar 413 Tetrazolium Tolerance Agar 413 Thayer–Martin Agar, Modified 413 Thayer–Martin Medium 414 Thayer–Martin Medium, Modified 415 Thayer–Martin Medium, Selective 416 Thayer–Martin Selective Agar 417 THIO + Bile Medium 418 THIO Medium 419 Thiogel ® Medium 417 Thioglycolate Bile Broth 417 Thioglycolate Broth USP, Alternative 418 Thioglycolate Gelatin Medium 418 Thioglycolate Medium 418 Thioglycolate Medium with 20% Bile 418 Thioglycolate Medium with Vitamin K1 and Hemin 419 Thioglycolate Medium without Glucose 420 Thioglycolate Medium without Glucose and Indicator 420 Thioglycolate Medium without Indicator 420 Thioglycolate Medium without Indicator with Hemin 421 Thioglycolate Medium without Indicator–135C 421 Thioglycolate Medium, Brewer 418, 419 Thioglycolate Medium, Brewer Modified 419 Thioglycolate Medium, Enriched 419 Thioglycolate Medium, Supplemented 421 Thioglycolate Medium, USP 421 Thioglycolate Peptone Glucose Yeast Extract Medium 433 Thiol Medium 422 Thiophene 2 Carboxylic Acid Hydrazide Medium 408
521
Thiosulfate Citrate Bile Salt Sucrose Agar 407 Thiotone E peptone 488 Throat 332, 451 Throat swabs 358 Tinsdale Agar 422 Tissierella creatinini 26 Tissue culture 122, 187, 337, 422, 423, 424, 425, 426, 427, 428, 429, 482 Tissue Culture Amino Acids, HeLa 100X 422 Tissue Culture Amino Acids, Minimal Eagle 50X 422 Tissue culture cells 99, 424 Tissue Culture Dulbecco Solution 423 Tissue Culture Earle Solution 423 Tissue Culture Hanks Solution 423 Tissue Culture Medium 199 423 Tissue Culture Medium Eagle with Earle Balanced Salt Solution 424 Tissue Culture Medium Eagle with Hanks Balanced Salt Solution 424 Tissue Culture Medium Eagle, HeLa 425 Tissue Culture Medium Ham F10 425 Tissue Culture Medium NCTC 109 426 Tissue Culture Medium RPMI #1640 427 Tissue Culture Minimal Medium Eagle 427 Tissue Culture Minimal Medium Eagle Spinner Modified 429 Tissue Culture Minimal Medium Eagle with Earle Balanced Salts Solution 428 Tissue Culture Tyrode Solution 429 Tissue Culture Vitamins Minimal Eagle, 100X 429 TMAO Medium 443 T–mycoplasmas 334, 335 TN Broth 445 TNSA Agar 443 TOC Agar 431 Todd–Hewitt Broth 431 Todd–Hewitt Broth, Modified 431 Toluidine Blue DNA Agar 432 Tonsillophilus suis 472 Toxoplasma gondii 432 Toxoplasma Medium 432 TPEY Agar 432 TPGY Broth 445 TPGY Medium 433 TPGYT Broth 446 Trace Element Mixture 491 Trace Element Solution HO-LE 433 Trace Elements Solution SL-6 491 Trace metals 433 Transgrow Medium 433, 434 Transgrow Medium with Trimethoprim 434 Transgrow Medium without Trimethoprim 435 Transport 25, 101, 111, 115, 116, 282, 334, 335, 375, 398, 405, 406, 434, 436, 471
522
Index
Transport Medium 435 Transport Medium Stuart 436 Trebouxia Agar 436 Trepomonas agilis 244 Treponema denticola 338, 345, 439 Treponema Isolation Medium 436 Treponema Medium 437, 438, 439, 440 Treponema Medium 1 440 Treponema Medium 2 440 Treponema Medium 3 440 Treponema Medium, Prereduced 441 Treponema oralis 345 Treponema pallidum 440 Treponema species 338, 440 Treponema vincentii 338 Treponemes 358, 370, 440, 441 Trichoderma longibrachiatum 13 Trichomonas Medium 441 Trichomonas Medium No. 2 441 Trichomonas Selective Medium 442 Trichomonas species 177, 272, 442, 460 Trichomonas vaginalis 167, 274, 441, 442, 460, 461 Trichosel Broth, Modified 442 Trimethylamine N–Oxide Medium 443 Triple Sugar Iron Agar 443 Tritrichomonas foetus 461 Trypaflavin Nalidixic Acid Serum Agar 443 Trypanoplasma borreli 282 Trypanosoma conorrhini 79, 178, 179 Trypanosoma cruzi 178, 179, 282, 337 Trypanosoma gambiense 444 Trypanosoma neveulemairei 273 Trypanosoma rangeli 178, 179 Trypanosoma rhodesiense 444 Trypanosoma species 67, 273 Trypanosome Medium 444 Tryptic Digest Broth 444 Tryptic Nitrate Medium 444 Tryptic Soy Agar 446 Tryptic Soy Agar with Magnesium Ions 32 Tryptic Soy Agar with Sodium Chloride 444, 445 Tryptic Soy Blood Agar 447 Tryptic Soy Broth with 0.1% Potassium Nitrate 449 Tryptic Soy Fast Green Agar 445 Trypticase 1% Solution 453 Trypticase Agar Base 445 Trypticase Agar Base with Carbohydrate 445 Trypticase Novobiocin Broth 445 Trypticase peptone 488 Trypticase Peptone Glucose Yeast Extract Broth 445 Trypticase Peptone Glucose Yeast Extract Broth with Trypsin 446 Trypticase Peptone Glucose Yeast Extract Broth, Buffered 446 Trypticase Soy Agar 446
Trypticase Soy Agar with Human Blood 446 Trypticase Soy Agar with Lecithin and Polysorbate 80 446 Trypticase Soy Agar with Sheep Blood 447 Trypticase Soy Agar with Sheep Blood and Gentamicin 448 Trypticase Soy Agar with Sheep Blood, Formate and Fumarate 447 Trypticase Soy Agar with Sheep Blood, Sucrose, and Tetracycline 448 Trypticase Soy Agar Yeast Extract 449 Trypticase Soy Agar, Modified 447 Trypticase Soy Broth with 10mM Glucose 449 Trypticase Soy Broth with Neomycin 450 Trypticase Soy Broth with Tobramycin 450 Trypticase Soy Broth with Tween 80 450 Trypticase Soy Broth with Yeast Extract 451 Trypticase Soy Broth without Glucose 450 Trypticase Sulfite Neomycin Agar 457 Trypticase Tellurite Agar Base 451 Trypticase Yeast Extract Glucose Medium 452 Trypticase Nitrate Broth 258 Trypticase Soy Agar with Sheep Blood and Tween 80 449 Trypticase Soy Agar with Sheep Blood and Vacnomycin 449 Trypticase Soy Agar with Tobramycin 448 Trypticase Soy Broth with 1.5% NaCl 450 Trypticase Soy Broth with 10 mM Glucose 449 Trypticase Soy Broth with Sheep Blood 450 Tryptone 487, 488 Tryptone Bile Glucuronide Agar, Harlequim 451 Tryptone Bile X-glucuronide Agar 407 Tryptone Bile X-glucuronide Agar, Chromocult 451 Tryptone Broth 429, 452 Tryptone Phosphate Broth 452 Tryptone Salt Agar 430 Tryptone Salt Broth 430 Tryptone Soya Agar 452 Tryptone Soya Broth 452 Tryptone Soya Broth with 0.1% Tween 80 452 Tryptone Soya Broth with Yeast Extract 452 Tryptone Water Broth 452 Tryptone Yeast Extract Agar 452 Tryptone Yeast Extract Agar 1 453 Tryptone Yeast Extract Glucose Salt Medium 459 Tryptophan 1% Solution 453 Tryptophan test 258 Tryptose 487, 488 Tryptose Agar 453 Tryptose Agar with Citrate 453 Tryptose Agar with Sheep Blood 453 Tryptose Agar with Thiamine 454 Tryptose Blood Agar 454 Tryptose Blood Agar Base with Yeast Extract 454
Index Tryptose Broth 454 Tryptose Broth with Citrate 455 Tryptose Cycloserine Dextrose Agar 455 Tryptose Phosphate Agar 455 Tryptose Phosphate Broth 455 Tryptose Phosphate Broth, Modified 455 Tryptose Sulfite Cycloserine Agar 456 Tryptose Sulfite Cycloserine Agar with Polymyxin and Kanamycin 456 Tryptose Sulfite Cycloserine Agar without Egg Yolk 456 Tryptose Sulfite Cycloserine Agar, Fluorocult 457 TSA Blood Agar 447 TSA II 447 TSA II with Sheep Blood and Gentamicin 448 Tsatumella ptyseos 237 TSAYE 449 TSC Agar 456 TSC Agar without Egg Yolk 456 TSC Agar, Fluorocult 457 TSFA 445 TSI Agar 443 TSN Agar 457 T-strain mycoplasmas 462, 463, 464 Tsukamurella paurometabolum 291 TT Broth 411 TT Broth, Hajna 412 TT Broth, USA 412 TTC Agar 413 Tuberculosis 310, 311 Tween 80 Hydrolysis Broth 458 Tween 80 Hydrolysis Medium 458 Tween 80 hydrolyzation 458 Tween 80 Oxgall Caffeic acid Agar 431 TY Medium 459 TY Salt Medium 459 TYGS Medium 459 TYI-S-33 Medium 459 TYM Basal Medium, Modified 1 460 TYM Basal Medium, Modified 2 460 TYM Basal Medium, Modified 4 460 Tyndallization 495 U Agar Plates 461 U Broth 461 U9 Broth 462 U9 Broth with Amphotericin B 463 U9B Broth 463 U9C Broth 464 University of Vermont Listeria Enrichment Broth 468 University of Vermont Modified Listeria Enrichment Broth 468 Urea Agar 464 Urea Agar Base 465 Urea Agar Base, Christensen 464
523
Urea Broth 467 Urea Broth 10B for Ureaplasma urealyticum 465 Urea Broth Base 466 Urea R Broth 466 Urea Rapid Broth 466 Urea Semisolid Medium 466 Urea Test Broth 467 Urea utilization 259 Ureaplasma Agar Plates 461 Ureaplasma Broth 461 Ureaplasma species 5, 6, 7, 8, 9, 20, 44, 86, 397, 461, 466, 467 Ureaplasma urealyticum 5, 6, 7, 8, 9, 20, 44, 178, 399, 462, 463, 464, 466 Urease 363, 463, 464, 465, 466 Urease Color Test Medium 462 Urease production 140, 465, 466, 467, 468 Urease Test Agar 464 Urease Test Broth 467 Urethral specimens 243 Urinary 369 Urinary tract infections 5, 6, 7, 9, 143, 144, 251 Urine 5, 6, 7, 8, 9, 20, 38, 84, 145, 297, 360, 361, 410, 411, 412, 413 Urogenital 334, 335 USP Alternative Thioglycolate Medium 401 UTI Agar, Modified HiCrome 250 UVM Listeria Enrichment Broth 468 UVM Modified Listeria Enrichment Broth 468 V Agar 468 V C A Inhibitor 493 V C A T Inhibitor 493 V C N Inhibitor 494 V C N T Inhibitor 494 V-8 Agar 468, 469 VA Vitamin Solution 491 Vaginal specimens 243, 378, 451 Vancomycin resistant enterococci 474 Veal Infusion Agar 469 Veal Infusion Broth 469 Veal Infusion Broth with Horse Serum 469 Veillonella Agar 469 Veillonella Medium 470 Veillonella Medium, DSM 470 Veillonella parvula 470 Veillonella Selective Medium 470 Veillonella species 375, 470 Vero tissue culture 122 Verotoxin-producing 445 Vibrio Agar 470 Vibrio alginolyticus 133, 142 Vibrio anguillarum 96 Vibrio cholerae 20, 22, 61, 33, 142, 158, 315, 340, 406, 408, 430, 431, 482, Vibrio hemolysin 475
524
Index
Vibrio mimicus 134, 482 Vibrio parahaemolyticus 81, 133, 142, 340, 406, 408, 471 Vibrio parahaemolyticus Sucrose Agar 471 Vibrio species 20, 22, 39, 123, 133, 171, 226, 227, 236, 293, 40, 345, 347, 348, 406, 430, 431, 444, 471 Vibrio vulnificus 340, 471 Violet Peptone Bile Lactose Broth 471 Violet Red Bile Lactose MUG Agar 473 Viral 425, 471 Viral Transport Medium 471 Viridans enterococci 315 Viridans streptococci 315 Viruses 422, 423, 424, 428 Vitamin B6 Blood Agar 471 Vitamin B6 Blood Agar with Pyridoxal-HCl 472 Vitamin free casamino acids 489 Vitamin K1 Solution 491 Vitox Supplement 491 VL Agar with Blood 472 VL Medium 472 Vogel and Johnson Agar 472 Voges-Proskauer Medium 473 Voges-Proskauer reaction 319 VP Medium 473 VPSA 471 VRB MUG Agar 473 VRE 474 VRE Agar 473, 474 VRE Broth 474 VTM 471 Wadowsky and Yee Medium, Modified 322 Wadowsky–Yee Medium 54 Wagatsuma Agar 475 Wallenstein Medium 475 Water 97, 100, 197 Wayne Sulfatase Agar 39 Wickerham Broth 475, 476 Wickerham Broth with Raffinose 476 Wilkins–Chalgren Agar 476 Wilkins–Chalgren Anaerobe Agar 477 Wilkins–Chalgren Anaerobe Agar with G–N Supplement 477 Wilkins–Chalgren Anaerobe Agar with N–S Supplement 477 Wilkins–Chalgren Anaerobe Broth 478 Wilson Blair Base 478 Winge Agar 478
Wolin–Bevis Medium 479 Wolinella species 137, 209 Worfel–Ferguson Agar 479 Wounds 150 Xanthine Agar 479 Xanthine utilization 479 XL Agar Base 479, 480 XLD Agar 480 XLT-4 480 XPS Agar 481 Xylose fermentation 480 Xylose Lactose Tergitol 4 480 Xylose Lysine Agar Base 479 Xylose Lysine Deoxycholate Agar 480 Xylose Sodium Deoxycholate Citrate Agar 481 Y 1 Adrenal Cell Growth Medium 481, 482 Y-1 adrenal assay 236 Y-1 mouse adrenal cells 482 Yeast 37, 75, 79, 81, 151, 252, 315, 484 Yeast Autolysate Growth Supplement 491 Yeast Beef Agar 35 Yeast Dialysate 491 Yeast Extract 491 Yeast Extract Agar 482, 483 Yeast Extract Sodium Lactate Medium 483 Yeast Extract Sucrose Agar 483 Yeast Fermentation Medium 483 Yeast Glucose Agar 484 Yeast phase 254, 380 Yeastolate 491 Yeastrel Agar 484 Yeasts 16, 40, 63, 114, 115, 206, 363, 382 YEPD Medium 484 Yersinia enterocolitica 30, 100, 121, 144, 159, 297, 374, 398, 485 Yersinia Isolation Agar 100 Yersinia pestis 62 Yersinia pseudotuberculosis 255 Yersinia Selective Agar 120, 144 Yersinia Selective Agar Base 484 Yersina Selective Supplement 494 Yersinia species 157, 159, 261, 340, 370 Yersinina enterocolitica 61 YESA 483 YI-S Medium 485 YPC Medium 485 YPNC Medium 485
